SYNTHESIS OF BACKBONE MODIFIED MORPHOLINO OLIGONUCLEOTIDES AND CHIMERAS USING PHOSPHORAMIDITE CHEMISTRY
20190218236 ยท 2019-07-18
Inventors
Cpc classification
C07H21/00
CHEMISTRY; METALLURGY
Y02P20/55
GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
C07F9/65616
CHEMISTRY; METALLURGY
C07H1/00
CHEMISTRY; METALLURGY
C07D413/04
CHEMISTRY; METALLURGY
C07F9/65586
CHEMISTRY; METALLURGY
C07F9/6561
CHEMISTRY; METALLURGY
C07F9/4461
CHEMISTRY; METALLURGY
C07F9/65583
CHEMISTRY; METALLURGY
C07D473/18
CHEMISTRY; METALLURGY
International classification
C07F9/6558
CHEMISTRY; METALLURGY
Abstract
Amine substituted morpholino oligonucleotides, other than the classical N,N-dimethylamino PMO analogue, and methods of efficiently synthesizing these oligonucleotides with high yield are provided. Morpholino oligonucleotides having thiophosphoramidate, phosphoramidate, and alkyl phosphoramidate linkers. Chimeras containing unmodified DNA/RNA and other analogs of DNA/RNA can be prepared. These oligonucleotides form duplexes with complementary DNA or RNA that are more stable than natural DNA or DNA/RNA complexes, are active with RNAse H1, and may be transfected into cells using standard lipid reagents. These analogues are therefore useful for numerous applications.
Claims
1. An oligomer comprising a monomer subunit comprising the chemical structure of formula I: ##STR00004## wherein: each B is independently a nucleic acid base (adenosine, guanosine, uracil, thymine, cytosine, innosine), or a nucleic acid base protected with a silyl protecting group or an acid-labile or base-labile protecting group; X is oxygen or sulfur, methyl, ethyl, any C.sub.3-7 alkyl, a 5-7 membered aliphatic or aromatic ring, carboxylate, acetate or formate derivatives, an amine, or amine substituted with any linear or branched C.sub.1-5 alkyl; Y is oxygen or sulfur, and, each R is independently linked to a glass substrate, a polystyrene resin, dimethoxytrityl protecting group, a phosphorus derivative, a DNA or RNA oligonucleoside/oligonucleotide, trimethoxytrityl, monomethoxy trityl, tritly, any silyl, or another morpholino of formula I, wherein the linker is phosphorodiamidate linker with phosphate/phosphorothioate/bornaphosphate linkages, or a phosphoroamidate linker, a phosphate linkage, or a thio linkage, or any other linkage with a morpholino ring with X.
2. The oligomer of claim 1, wherein the nucleic acid base protecting group is selected from: ##STR00005##
3. The oligomer of claim 1, comprising between 2 and 40 monomeric subunits.
4. A phosphoramidite synthon having a chemical structure: ##STR00006## wherein: B is independently a nucleic acid base selected from adenosine, guanosine, uracil, thymine, cytosine, and inosine, or a nucleic acid base protected with a silyl protecting group or an acid-labile or base-labile protecting group; R.sup.1 and R.sup.2 are independently alkyl or aryl optionally substituted with one or more heteroatoms; R.sup.3 is a protecting group that is easily removed following synthesis of an oligonucleotide, such as cyanoethyl or methyl; R.sup.4 is a linker selected from a phosphorodiamidate linker, a phosphate linkage, a thio linker, or a phosphorodimidate linker with phosphate/phosphorothioate/bornaphosphate linkages; wherein the linker is linked to dimethoxytrityl protecting group, a phosphorus derivative, a DNA or RNA oligonucleoside/oligonucleotide, trimethoxytrityl, monomethoxy trityl, tritly, any silyl, or another morpholino of formula I.
5. The phosphoramidite synthon of claim 4, wherein the nucleic acid base protecting group is selected from: ##STR00007##
6. A method of preparing a phosphorodiamidite monomer comprising: a. contacting a 5-O-Dimethoxytrityl ribo-base with sodium periodate and ammonium biborate to produce a dihydroxyribose morpholino monomer, wherein the base is one of thymidine, cytosine, adenine, and guanine, optionally protected at the nucleoside amino groups by a protecting group, b. reducing hydroxyl groups on the dihydroxyribose morpholino monomer with sodium cyanoborohydride to produce a morpholino monomer, and c. phosphitylating the morpholino monomer with 2-cyanoethyl-N,N,N,N-tetraisopropylphosphordiamidite and 4,5-dicyanoimidazole (DCI) in dichloromethane to produce a phosphorodiamidite monomer.
7. The method of claim 6, wherein the protecting group at the nucleoside amino groups is any protecting group of claim 4 or claim 5.
8. A method of forming an oligomer comprising at least one monomeric subunit of claim 1, comprising: a. providing a 5-unprotected-2-deoxyribonucleoside linked to a polystyrene/CPG support; b. reacting the 5-unprotected-2-deoxyribonucleoside with a phosphoramidite of claim 4 in anhydrous acetonitrile containing 4,5-dicyanoimidazole (DCI) to generate a dimer having a phosphoramidite diester internucleotide linkage; c. chemically activating the dimer comprising at least one of boronating, sulfurizing, or oxidizing the dimer, d. capping the dimer, e. detritylating the dimer, f. repeating steps b. to e. to elongate the oligomer, g. contacting morpholino borane phosphoroamidate monomers with iodine and an amine in tetrahydrofuran to convert morpholino phosphoroamidate to amino-PMOs, h. contacting the oligomers with a solution comprising ammonium hydroxide and ethylene diamine to remove the oligomer from the polystyrene support.
9. The method of claim 8, wherein the activating step c. comprises boronating the dimer and further comprising the additional step of: removing cyanoethyl groups from the internucleotide linkages after the elongating step f and before the contacting step g.
10. The method of claim 8, wherein the activating step c. comprises boronating the dimer and further comprising the additional step of: contacting the monomers with a solution of tetrabutyl ammonium fluoride (TBAF) in THF to remove BIBS protecting groups from the monomers, after the contacting step g and before step h.
11. The method of claim 8, wherein the repeating synthesis step f is conducted on a commercial DNA synthesizer.
12. The method of claim 8, wherein after sulfurizing to generate a thiomorpholino linkage the oligomer synthesized comprises at least one monomer subunit of claim 1.
13. An oligonucleotide of claim 1, comprising thiomorpholino internucleotide linkages that readily form duplexes with complementary DNA or RNA that are more stable than natural DNA or DNA/RNA complexes.
14. An oligonucleotide of claim 1, that activates RNAse H1 enzymatic activity.
15. An oligonucleotide of claim 1, that inactivates enzymatic activity.
16. An oligonucleotide of claim 1, that is readily transfected into cells using standard lipid reagents.
Description
BRIEF DESCRIPTION OF FIGURES
[0015]
[0016]
[0017]
[0018]
[0019]
[0020]
[0021]
DESCRIPTION OF EMBODIMENTS
[0022] The terms below have the following meanings, unless indicated otherwise:
[0023] The term oligonucleotide analog refers to oligonucleotide having a modified backbone structure, e.g., a backbone other than the standard phosphodiester linkage found in natural oligo- and polynucleotides, and optionally, modified sugar moieties, e.g., morpholino moieties rather than ribose or deoxyribose moieties. The analog supports bases capable of hydrogen bonding by Watson-Crick base pairing to standard polynucleotide bases, where the analog backbone presents the bases in a manner to permit such hydrogen bonding in a sequence-specific fashion between the oligonucleotide analog molecule and bases in a standard polynucleotide (e.g., single-stranded RNA or single-stranded DNA). Preferred analogs are those having a substantially uncharged, phosphorus containing backbone.
[0024] A nucleic acid base is not particularly limited as long as it can be used for the synthesis of nucleic acid and includes, for example, a pyrimidine base such as cytosine group, uracil group, thymine group and the like, and a purine base such as adenine group, guanine group and the like. The optionally protected nucleic acid base means, for example, that an amino group may be protected in an adenine group, a guanine group, or a cytosine group, which is a nucleic acid base having an amino group, and a nucleic acid base wherein the amino group therein is protected by a protecting group sustainable under the deprotection conditions of the morpholine ring nitrogen atom of the morpholino nucleotide is preferable.
[0025] The amino-protecting group is not particularly limited, and examples thereof include the protecting groups described in Greene's PROTECTIVE GROUPS IN ORGANIC SYNTHESIS, 4th edition, Wiley-Interscience, 2006 and the like. Specific examples of the amino-protecting group include a pivaloyl group, a pivaloyloxymethyl group, a trifluoroacetyl group, a phenoxyacetyl group, a 4-isopropylphenoxyacetyl group, a 4-tert-butylphenoxyacetyl group, an acetyl group, a benzoyl group, an isobutyryl group, a dimethylformamidinyl group, a 9-fluorenylmethyloxycarbonyl group and the like. Among them, a phenoxyacetyl group, a 4-isopropylphenoxyacetyl group, an acetyl group, a benzoyl group, an isobutyryl group and a dimethylformamidinyl group are preferable. In addition, the carbonyl group of the nucleic acid base is optionally protected, and can be protected, for example, by reacting phenol, 2,5-dichlorophenol, 3-chlorophenol, 3,5-dichlorophenol, 2-formylphenol, 2-naphthol, 4-methoxyphenol, 4-chlorophenol, 2-nitrophenol, 4-nitrophenol, 4-acetylaminophenol, pentafluorophenol, 4-pivaloyloxybenzyl alcohol, 4-nitrophenethyl alcohol, 2-(methyl sulfonyl)ethanol, 2-(phenyl sulfonyl)ethanol, 2-cyanoethanol, 2-(trimethylsilyl)ethanol, dimethylcarbamoyl chloride, diethylcarbamoyl chloride, ethylphenylcarbamoyl chloride, 1-pyrrolidinecarbonyl chloride, 4-morpholinecarbonyl chloride, diphenylcarbamoyl chloride and the like.
[0026] In some cases, the carbonyl-protecting group does not need to be particularly introduced. Moreover, in addition to the above-mentioned groups, a modified nucleic acid base (e.g., a 8-bromoadenyl group, a 8-bromoguanyl group, a 5-bromocytosyl group, a 5-iodocytosyl group, a 5-bromouracil group, a 5-iodouracil group, a 5-fluorouracil group, a 5-methylcytosyl group, a 8-oxoguanyl group, a hypoxanthinyl group etc.), which is a nucleic acid base substituted by any 1 to 3 substituents (e.g., a halogen atom, an alkyl group, an aralkyl group, an alkoxy group, an acyl group, an alkoxyalkyl group, a hydroxy group, an amino group, monoalkylamino, dialkylamino, carboxy, cyano, nitro etc.) at any position(s), are also encompassed in the nucleic acid base.
[0027] A substantially uncharged, phosphorus containing backbone in an oligonucleotide analog is one in which a majority of the subunit linkages, e.g., between 60-100%, are uncharged at physiological pH, and contain a single phosphorous atom. The analog contains between 5 and 40 subunits, typically about 8-25 subunits, and preferably about 12 to 25 monomeric subunits. The analog may have exact sequence complementarity to the target sequence or near complementarity, as defined below.
[0028] A monomer or subunit of an oligonucleotide analog refers to one nucleotide (or nucleotide analog) unit of the analog. The term may refer to the nucleotide unit with or without the attached inter-subunit linkage, although, when referring to a charged subunit, the charge typically resides within the inter-subunit linkage (e.g. a phosphate or phosphorothioate linkage).
[0029] A morpholino oligonucleotide analog is an oligonucleotide analog composed of morpholino subunit structures. Exemplary structures are shown side-by-side (for comparative purposes) in
[0030] The subunits and linkages shown in
[0031] A preferred morpholino oligomer is either a phosphorodiamidate-linked morpholino oligomer, referred to herein as a PMO or a morpholino oligomer referred to herein as a TMO or TMO/DNA chimera. Such oligomers are composed of morpholino subunit structures such as shown in
[0032] The term substituted, particularly with respect to an alkyl, alkoxy, thioalkoxy, or alkylamino group, refers to replacement of a hydrogen atom on carbon with a heteroatom-containing substituent, such as, for example, halogen, hydroxy, alkoxy, thiol, alkylthio, amino, alkylamino, imino, oxo (keto), nitro, cyano, or various acids or esters such as carboxylic, sulfonic, or phosphonic. It may also refer to replacement of a hydrogen atom on a heteroatom (such as an amine hydrogen) with an alkyl, carbonyl or other carbon containing group.
[0033] Sequences are described as complementary to one another when hybridization occurs in an antiparallel configuration. A double-stranded polynucleotide can be complementary to another polynucleotide. A targeting sequence may have near or substantial complementarity to the target sequence and still function for the purpose of the present invention. Preferably, the oligonucleotide analogs of this disclosure have at most one mismatch with the target sequence out of 10 nucleotides, and preferably at most one mismatch out of 20. Alternatively, the antisense oligomers of this disclosure have at least 90% sequence homology, and preferably at least 95% sequence homology, with the exemplary targeting sequences as designated herein. Thus, the oligomers made by the methods of this disclosure are particularly useful as therapeutic antisense molecules when administered to treat a disease state amenable to antisense therapy.
[0034] An oligonucleotide analog specifically hybridizes to a target polynucleotide if the oligomer hybridizes to the target under physiological conditions, with a Tm substantially greater than 45 C., preferably at least 50 C., and typically 60 C.-80 C., or higher. Such hybridization preferably corresponds to stringent hybridization conditions. At a given ionic strength and pH, the Tm is the temperature at which 50% of a target sequence hybridizes to a complementary polynucleotide. Again, such hybridization may occur with near or substantial complementarity of the antisense oligomer to the target sequence, as well as with exact complementarity.
[0035] A nuclease-resistant oligomeric molecule (oligomer) refers to one whose backbone is substantially resistant to nuclease cleavage, in non-hybridized or hybridized form; by common extracellular and intracellular nucleases in the body; that is, the oligomer shows little or no nuclease cleavage under normal nuclease conditions in the body to which the oligomer is exposed.
[0036] A heteroduplex refers to a duplex between an oligonucleotide analog and the complementary portion of a target RNA. A nuclease-resistant heteroduplex refers to a heteroduplex formed by the binding of an antisense oligomer to its complementary target, such that the heteroduplex is substantially resistant to in vivo degradation by intracellular and extracellular nucleases, such as RNAseH, which are capable of cutting double-stranded RNA/RNA or RNA/DNA complexes.
[0037] The oligonucleotide analogs of this disclosure preferably specifically bind to a target RNA sequence inside a cell. The base specificity of such binding is sequence specific. For example, a single-stranded polynucleotide can specifically bind to a single-stranded polynucleotide that is complementary in sequence.
[0038] As detailed above, the antisense oligomer has a base sequence directed to a targeted portion of the viral genome, preferably either the 5-CS or 3-CS. In addition, the oligomer is able to effectively target infecting viruses, when administered to an infected host cell, e.g. in an infected animal subject. This requirement is met when the oligomer compound (a) has the ability to be actively taken up by mammalian cells, and (b) once taken up, form a duplex with the target ssRNA with a Tm greater than about 50 C.
[0039] As will be described below, the ability to be taken up by cells requires that the oligomer backbone be substantially uncharged, and, preferably, that the oligomer structure is recognized as a substrate for active or facilitated transport across the cell membrane. The ability of the oligomer to form a stable duplex with the target RNA will also depend on the oligomer backbone, as well as factors noted above, the length and degree of complementarity of the antisense oligomer with respect to the target, the ratio of G:C to A:T base matches, and the positions of any mismatched bases. The ability of the antisense oligomer to resist cellular nucleases promotes survival and ultimate delivery of the oligomer to the cell cytoplasm.
[0040] The following methods are useful for testing any given, substantially uncharged backbone for its ability to meet these requirements:
Active or Facilitated Uptake by Cells
[0041] The antisense oligomer may be taken up by host cells by facilitated or active transport across the host cell membrane if administered in free (non-complexed) form, or by an endocytotic mechanism if administered in complexed form.
[0042] In the case where the agent is administered in free form, the antisense compound should be substantially uncharged, meaning that a majority of its inter-subunit linkages are uncharged at physiological pH. Experiments carried out in support of this technology indicate that a small number of net charges, e.g., 1-2 for a 15- to 20-mer oligomer, can in fact enhance cellular uptake of certain oligomers with substantially uncharged backbones. The charges may be carried on the oligomer itself, e.g., in the backbone linkages, or may be terminal charged-group appendages. Preferably, the number of charged linkages is no more than one charged linkage per four uncharged linkages. More preferably, the number is no more than one charged linkage per ten, or no more than one per twenty, uncharged linkages. In one embodiment, the oligomer is fully uncharged.
[0043] An oligomer may also contain both negatively and positively charged backbone linkages, as long as opposing charges are present in approximately equal number. Preferably, the oligomer does not include runs of more than 3-5 consecutive subunits of either charge. For example, the oligomer may have a given number of anionic linkages, e.g. phosphorothioate or N3.fwdarw.P5 phosphoramidate linkages, and a comparable number of cationic linkages, such as N,N-diethylenediamine phosphoramidates. The net charge is preferably neutral or at most 1-2 net charges per oligomer.
[0044] In addition to being substantially or fully uncharged, the antisense agent is preferably a substrate for a membrane transporter system (i.e., a membrane protein or proteins) capable of facilitating transport or actively transporting the oligomer across the cell membrane. This feature may be determined by one of a number of tests for oligomer interaction or cell uptake, as follows.
[0045] A first test assesses binding at cell surface receptors, by examining the ability of an oligomer compound to displace or be displaced by a selected charged oligomer on a cell surface. The cells are incubated with a given quantity of test oligomer, which is typically fluorescently labeled, at a final oligomer concentration of between about 10-300 nM. Shortly thereafter, e.g., 10-30 minutes (before significant internalization of the test oligomer can occur), the displacing compound is added, in incrementally increasing concentrations. If the test compound is able to bind to a cell surface receptor, the displacing compound will be observed to displace the test compound. If the displacing compound is shown to produce 50% displacement at a concentration of 10 the test compound concentration or less, the test compound is considered to bind at the same recognition site for the cell transport system as the displacing compound.
[0046] A second test measures cell transport, by examining the ability of the test compound to transport a labeled reporter, e.g., a fluorescence reporter, into cells. The cells are incubated in the presence of labeled test compound, added at a final concentration between about 10-300 nM. After incubation for 30-120 minutes, the cells are examined, e.g., by microscopy, for intracellular label. The presence of significant intracellular label is evidence that the test compound is transported by facilitated or active transport.
[0047] The antisense compound may also be administered in complexed form, where the complexing agent is typically a polymer, e.g., a cationic lipid, polypeptide, or non-biological cationic polymer, having an opposite charge to any net charge on the antisense compound. Methods of forming complexes, including bilayer complexes, between anionic oligonucleotides and cationic lipid or other polymer components, are well known. For example, the liposomal composition Lipofectin, containing the cationic lipid DOTMA (N-[1-(2,3-dioleyloxy)propyI]-N,N,N-trimethylammonium chloride) and the neutral phospholipid DOPE (dioleyl phosphatidyl ethanolamine), is widely used. After administration, the complex is taken up by cells through an endocytotic mechanism, typically involving particle encapsulation in endosomal bodies.
[0048] The antisense compound may also be administered in conjugated form with an arginine-rich peptide linked to the 5 or 3 end of the antisense oligomer. The peptide is typically 8-16 amino acids and consists of a mixture of arginine, and other amino acids including phenyalanine and cysteine. Exposure of cells to the peptide conjugated oligomer results in enhanced intracellular uptake and delivery to the RNA target.
[0049] Alternatively, the requisite properties of oligomers with any given backbone can be confirmed by a simple in vivo test, in which a labeled compound is administered to an animal, and a body fluid sample, taken from the animal several hours after the oligomer is administered, is assayed for the presence of heteroduplex with target RNA.
Substantial Resistance to RNaseH
[0050] Two general mechanisms have been proposed to account for inhibition of expression by antisense oligonucleotides. In the first, a heteroduplex formed between the oligonucleotide and the viral RNA acts as a substrate for RNaseH, leading to cleavage of the target RNA. Oligonucleotides belonging, or proposed to belong, to this class include phosphorothioates, phosphotriesters, and phosphodiesters (unmodified natural oligonucleotides). Such compounds expose the viral RNA in an oligomer:RNA duplex structure to hydrolysis by RNaseH, and therefore loss of function.
[0051] A second class of oligonucleotide analogs, termed steric blockers or, alternatively, RNaseH inactive or RNaseH resistant, have not been observed to act as a substrate for RNaseH, and are believed to act by sterically blocking target RNA nucleocytoplasmic transport, splicing, translation, or replication. This class includes methylphosphonates, morpholino oligonucleotides, peptide nucleic acids (PNA's), certain 2-O-allyl or 2-O-alkyl modified oligonucleotides, and N3.fwdarw.P5 phosphoramidates.
[0052] A test oligomer can be assayed for its RNaseH resistance by forming an RNA:oligomer duplex with the test compound, then incubating the duplex with RNaseH under standard assay conditions. After exposure to RNaseH, the presence or absence of intact duplex can be monitored by gel electrophoresis or mass spectrometry.
In Vivo Uptake
[0053] Rapid tests exist for confirming that a given antisense oligomer type provides the required characteristics noted above, namely, high Tm, ability to be actively taken up by the host cells, and substantial resistance to RNaseH. This method is based on the discovery that a properly designed antisense compound will form a stable heteroduplex with the complementary portion of the target RNA when administered to a mammalian subject, and the heteroduplex subsequently appears in the urine (or other body fluid). Details of this method are given in U.S. patent application Ser. No. 09/736,920, entitled Non-Invasive Method for Detecting Target RNA (Non-Invasive Method), the disclosure of which is incorporated herein by reference. Briefly, a test oligomer containing a backbone to be evaluated, having a base sequence targeted against a known RNA, is injected into an animal, e.g., mammalian subject. The antisense oligomer may be directed against any intracellular RNA, including a host RNA or the RNA of an infecting virus. Several hours (typically 8-72) after administration, the urine is assayed for the presence of the antisense-RNA heteroduplex. If heteroduplex is detected, the backbone is suitable for use in the antisense oligomers of the present invention.
[0054] The oligomer may be labeled, e.g. by a fluorescent or a radioactive tag, to facilitate subsequent analyses, if it is appropriate for the mammalian subject. The assay can be in any suitable solid-phase or fluid format. Generally, a solid-phase assay involves first binding the heteroduplex analyte to a solid-phase support, e.g., particles or a polymer or test-strip substrate, and detecting the presence/amount of heteroduplex bound. In a fluid-phase assay, the analyte sample is typically pretreated to remove interfering sample components. If the oligomer is labeled, the presence of the heteroduplex is confirmed by detecting the label tags. For non-labeled compounds, the heteroduplex may be detected by immunoassay if in solid phase format or by mass spectroscopy or other known methods if in solution or suspension format.
Exemplary Oligomer Backbones
[0055] Examples of nonionic linkages that may be used in oligonucleotide analogs are shown in
[0056] A preferred oligomer structure employs morpholino-based subunits bearing base-pairing moieties, joined by uncharged linkages. Morpholino oligonucleotides, including antisense oligomers, are detailed, for example, in co-owned U.S. Pat. Nos. 5,698,685; 5,217,866; 5,142,047; 5,034,506; 5,166,315; 5,185,444; 5,521,063; and 5,506,337, all of which are expressly incorporated by reference herein.
[0057] Important properties of the morpholino-based subunits include: the ability to be linked in an oligomeric form by stable, uncharged backbone linkages; the ability to support a nucleotide base (e.g. adenine, cytosine, guanine or uracil) such that the polymer formed can hybridize with a complementary-base target nucleic acid, including target RNA, with high Tm, even with oligomers as short as 10-14 bases; the ability of the oligomer to be actively transported into mammalian cells; and the ability of the oligomer:RNA heteroduplex to resist RNAse degradation.
[0058] Backbone structures for antisense oligonucleotides of this disclosure include the morpholino subunit types shown in
[0059] As noted above, the substantially uncharged oligomer may advantageously include a limited number of charged linkages, e.g. up to about 1 per every 5 uncharged linkages, more preferably up to about 1 per every 10 uncharged linkages. Therefore, a number of charged linkages, e.g. charged phosphoramidate or phosphorothioate, may also be incorporated into the oligomers.
[0060] Another aspect of this disclosure provides methods of producing morpholino-containing oligonucleotide analogs, comprising starting with a 5-unprotected-2-deoxyribonucleoside linked to a polystyrene support, and reacting this 5-unprotected-2-deoxyribonucleoside with a phosphoramidite synthon (i.e., monomer) in anhydrous acetonitrile containing 4,5-dicyanoimidazole (DCI) to generate a dimer having a phosphoramidite diester internucleotide linkage. The dimer is then chemically activated by either boronating, sulfurizing, or oxidizing the dimer. The dimer is then capped and detritylated. These steps (adding a phosphoramidite synthon through the steps of capping and detritylating) are repeated as desired to elongate the oligomer by adding monomers to the growing oligomer (growing step-wise from a dimer, to a trimer, to a tetramer, pentamer, hexamer, etc.). The morpholino phosphoroamidate oligomers are then contacted with iodine and dimethylamine in tetrahydrofuran to convert morpholino boranephosphoroamidate to N,N-dimethylamino PMOs. The oligomers are then contacted with a solution comprising ammonium hydroxide and ethylene diamine to remove the oligomer from the polystyrene support. These repetitive monomer additions to the oligomer may be performed on a common commercial DNA synthesizer, thereby greatly enhancing the efficiency and speed of the synthesis in a cost-effective manner.
[0061] Exemplary monomers for use in the synthesis methods of this disclosure include phosphordiamidites having a chemical structure selected from the group consisting of:
##STR00001## ##STR00002##
[0062] Wherein:
B or B* may be a silyl protecting group, or acid labile or base labile protecting group;
X=Cyanoethyl or its derivative, alkyl, thio alkyl, thio carbonyl, carboxylate, acetate, or formate derivatives
R=Dimethoxytrityl, trimethoxyltrityl, or any silyl based protecting group
R.sub.1 and R.sub.2 are independently isopropyl, C.sub.2-20 linear or branched alkyl chain, or a 5-7 membered aliphatic ring.
[0063] Each publication or patent cited herein is incorporated herein by reference in its entirety.
[0064] The disclosure now being generally described will be more readily understood by reference to the following examples, which are included merely for the purposes of illustration of certain aspects of the embodiments of the present disclosure. The examples are not intended to limit the disclosure, as one of skill in the art would recognize from the above teachings and the following examples that other techniques and methods can satisfy the claims and can be employed without departing from the scope of the claimed disclosure.
EXAMPLES
Example 1
Synthesis of N-Di-Tertbutylisobutyl Protected Morpholino Phosphoradimidites
[0065] Phosphoradiamidite synthons were developed for all four bases that are needed to generate the boranephosphoramidate morpholino linkages (see the synthesis scheme of
[0066] The inventors also synthesized 5-dimethoxytrityl-morpholinothymidine-3-O-methyl-N,N-diisopropylphosphoradiamidite following a similar protocol, but the solid phase coupling with the cyanoethyl phosphoradiamidite was found to be more efficient than the O-methyl counterpart.
[0067] Synthesis of the corresponding monomers of cytosine, adenine, and guanine was initiated by first protecting the nucleoside amino groups with bis(tert-butyl)isobutylsilyl (BIBS) using a variation of the protocol reported previously (Roy, S., Olesiak, M., Shang, S., Caruthers, M. H., J. Am. Chem. Soc. 2013, 135:6234-41).
[0068] The reaction of 5,3,2-tri-O-acetylcytidine (10) with BIBS-OTf (Tf=triflate) in the presence of 2,6-lutidine gave 76% yield of the BIBS-protected cytidine after 2 h stirring at 60 C. under an argon atmosphere. But the synthesis of the corresponding adenine and guanosine required much longer reaction times (3 days) with yields of 25-31% for BIBS-protected guanosine and 74% for the corresponding adenosine derivative. As depicted in the synthesis scheme of
General Procedure for Synthesis of Morpholino Nucleosides.
[0069] 5-Dimethoxytrityl protected nucleosides were dissolved in methanol followed by addition of 1.2 equivalents of sodium periodate and ammonium biborate tetrahydrate (1.2 equivalents). Mixtures were stirred at room temperature for three hours when TLC indicated complete consumption of starting material. The reaction mixtures were filtered through a pad of celite and added to activated, powdered 4 A molecular sieves (0.4 g/mmol) followed by addition of 2.0 equivalents each of sodium cyanoborohydride and glacial acetic acid. Reaction mixtures were then stirred for 4-5 h when the intermediate diol was completely reduced. Reaction mixtures were filtered through a pad of celite and evaporated to dryness. Products were dissolved in chloroform and washed with saturated NaHCO.sub.3 and brine. Organic layers were collected, dried over Na.sub.2SO.sub.4 and filtered, and solvent removed under reduced pressure. Products were purified by flash chromatography on a silica gel column. In all cases, the silica gel slurries were prepared with the starting eluant mixture containing an additional 5% triethylamine. After pouring the slurry, columns were washed with two column volumes of the starting solvent mixture containing no triethylamine. Compounds 15, 16, and 17 in
[0070] 5-Dimethoxytritylmorpholinothymidine (compound 15,
[0071] N.sup.4-Di(tert-butyl)isobutylsilyl-5-dimethoxytritylmorphohnocytidine (compound 16,
[0072] N.sup.6-Di(tert-butyl)isobutylsilyl-5-dimethoxytritylmorpholinoadenosine (compound 17,
[0073] N.sup.2O.sup.6-Bis[di(tert-butyl)isobutylsilyl-5-dimethoxytritylmorpholino guanosine (compound 18,
[0074] Referring again to
[0075] The 5-O-DMT-N-BIBS protected morpholino nucleosides (compounds 16, 17, and 18,
[0076] 5-O-Dimethoxytritylmorpholinothymine-3-O-cyanoethyl-N,N-diisopropyl phosphordiamidite (compound 19,
[0077] N.sup.4-Di(tert-butyl)isobutylsilyl-5-dimethoxytrityl-morpholinocytosine-3-O-cyanoethyl-N,N-diisopropylphosphordiamidite (compound 20,
[0078] N.sup.6-Di(tert-butyl)isobutylsilyl-5-dimethoxytritylmorpholinoadenine-3-O-cyanoethyl-N,N-diisopropylphosphordiamidite (compound 21,
[0079] N.sup.2,O.sup.6-bis[di(tert-butyl)isobutylsilyl]-5-dimethoxytrityl-morpholinoguanine-3-O-cyanoethyl-N,N-diisopropylphosphoradiamidite (compound 22,
[0080] For the synthesis of PMO-DNA chimeras, 5-DMT-2-deoxyribonucleoside-3-phosphoramidite synthons (compounds 26, 27 and 28,
General Method for the Synthesis of Compounds 26, 27, and 28 of FIG. 3A
[0081] The 5-dimethoxytrityl-N-BIBS protected 2-deoxynucleoside was added to a round bottom flask flushed with argon. Anhydrous dichloromethane and 2-cyanoethyl-N,N,N,N-tetraisopropylphosphorodiamidite (1.2 equivalents) were added via syringe. 1.0 equivalent of tetrazole (0.4 M in CH.sub.3CN obtained from Glen Research) was added drop-wise to this solution over one-half hour while stirring. The reaction was stirred at room temperature for 2-3 hours at which time TLC showed complete disappearance of the starting material. The reaction mixture was diluted in dichloromethane and extracted twice with a saturated solution of NaHCO.sub.3. The organic layer was dried over Na.sub.2SO.sub.4, filtered and evaporated to dryness. The product was purified by flash chromatography on a silica column. The silica gel slurry was prepared with the starting eluant mixture containing an additional 5% triethylamine. After pouring the slurry, the column was washed with two column volumes of the starting solvent mixture containing no triethylamine. Compounds 24 and 25 of
[0082] N.sup.4-Di(tert-butyl)isobutylsilyl-5-dimethoxytrityl-2-deoxycytidine3-O-cyanoethyl-N,N-diisopropylphosphoramidite (compound 26,
[0083] N.sup.6-Di(tert-butyl)isobutylsilyl-5-dimethoxytrityl-2-deoxyadenosine3-O-cyanoethyl-N,N-diisopropylphosphoramidite (compound 27,
[0084] N.sup.2-Di(tert-butyl)isobutylsilyl-5-dimethoxytrityl-2-deoxyguanosine3-O-cyanoethyl-N,N-diisopropylphosphoramidite (compound 28,
Example 2
Synthesis of Morpholino Oligonucleotides Using BIBS-Protected Morpholino Phosphoradiamidites
[0085] Once the synthons described in Example 1 were available, the next goal was to optimize the solid-phase synthesis cycle for preparing borane phosphoroamidate morpholino derivatives, and for converting these compounds to the corresponding PMOs. The synthesis cycle is outlined in
[0086] The 5-unprotected-2-deoxyribonucleoside (
TABLE-US-00001 TABLE 1 Synthesis cycle for preparing PMOs and PMO-DNA chimeras. Reactions Wash/reagents/solvents Time (s) Detritylation 10% TMPB + 0.5% TFA in CHCl.sub.3 Flow 45 s Wash MeOH Flow 20 s, wait 10 s, flow 10 s. Condensation 0.1M phosphordiamidite 18, 19, 20, or 21 (in CH.sub.3CN) + Wait 300 s Activator (0.12M dicyanoimidazole in CH.sub.3CN) or 0.1M phosphoramidite 22, 23, 24, or 25 in CH.sub.3CN + Wait 180 s Activator (0.25M 5-(ethylthio)-1H-tetrazole (ETT) in CH.sub.3CN) Boronation 0.05M BH.sub.3THF in THF Flow 15 s, wait 45 s or 0.02M iodine in THF/water/pyridine Flow 8 s, wait 15 s Oxidation Wash Anhydrous CH.sub.3CN Flow 10 s Capping Cap A (THF/Pyridine/Ac.sub.2O) + Flow 10 s, wait 5 s Cap B (16% 1-methylimidazole in THF) Wash Anhydrous CH.sub.3CN Flow 10 s Wash Anhydrous CH.sub.2Cl.sub.2 Flow 25 s
[0087] Post synthesis, supports were washed with acetonitrile, treated with a 1:1 mixture of triethylamine:acetonitrile for 600 s in order to remove the cyanoethyl groups from internucleotide linkages (
[0088] To convert the morpholino borane phosphoroamidates to the N,N-dimethylamino PMOs, the morpholino borane phosphoroamidates were treated overnight with a solution of 0.05 M iodine and 2.0 M dimethylamine in tetrahydrofuran (
[0089] When oxidative amination reactions were carried out after removal of silyl protecting groups, amine substitution at the N-4 of cytosine was observed (
[0090] Once the silyl groups were removed, oligonucleotides were cleaved from supports using 30% ammonium hydroxide (
[0091] This synthesis was carried out on an ABI 394 Synthesizer. All syntheses were performed at a 0.2 micromol scale using a 5-DMT 2-deoxythymidine joined to a low volume polystyrene solid support via a succinate linkage. For synthesis of morpholino oligonucleotides, a standard 0.2 micro mole synthesis cycle was used with an increased coupling time of 300 s. A wash with methanol followed the detritylation step. All the phosphordiamidites (compounds 18, 19, 20, or 21 of
[0092] The vials containing resins were centrifuged at 4000 rpm and the supernatants removed with a pipette. Subsequently, resins were washed 4-5 times with 2 mL aliquots of acetonitrile, shaken vigorously, placed in a centrifuge at 4000 rpm for 5 minutes and supernatants removed. For amino-modified morpholino derivatives, the ammonia solution in isopropanol was removed under vacuum. These morpholino oligonucleotides were desilylated by overnight fluoride (1.0 mL of 1.0 M solution of tetrabutylammonium fluoride in THF) treatment. The resins were then treated with 1 mL of 37% ammonium hydroxide in water for 1 h in order to remove the product from the resins and the polystyrene resin beads were removed using a 0.2 m centrifugal filter.
[0093] The total volume of each solution was diluted to 2.5 mL by adding 0.5 mL Milipore water and the PMOs were desalted using Illustra NAP-25 Columns (GE Healthcare). Initially, these columns were equilibrated with 25.0 mL of water. After allowing water to completely enter the gel beds by gravity flow, 2.5 mL of samples were loaded onto columns and the purified samples were eluted using 3.5 mL Milipore water. Second step purifications were carried out for oligonucleotides having more than 10 nucleotides by using AMICON Ultra-4 3K devices. Solutions that accumulated after Nap column purification (3.5 mL total volume) were loaded on to Amicon devices and centrifuged at 4000g for 30 minutes. Concentrated solutes were washed with 3.0 mL2 of Milipore water in similar fashion. The oligonucleotides were collected and used for various experiments.
[0094] Incorporation of the uridine morpholino phosphordiamidite (similar to compound 18 of
[0095] Using this synthesis procedure outlined in
TABLE-US-00002 TABLE 2 Mass analysis (LCMS) of PMO and PMO-DNA chimeras (ODNs). Oligonucleotides containing N,N-dimethylamino-phosphorodiamidate (*) and phosphate (p) internucleotide linkages are shown. Morpholino and 2-deoxyribonucleosides are shown as upper and lower case letters respectively. Mol wt NO ODNs Cal Obs ODN 1 T*T*T*T*T*T*T*T*T*t 3214.00 3214.01 ODN 2 T*T*T*T*T*T*T*T*T*T*T*T*T*T*T*T*T*T*T*T*t 6846.17 6848.14 ODN 3 C*C*C*T*T*T*T*T*T*T*T*t 3829.36 3828.16 ODN 4 A*A*A*T*T*T*T*T*T*T*T*t 3901.44 3902.30 ODN 5 G*G*T*T*T*T*T*T*T*T*T*t 3924.42 3925.26 ODN 6 G*A*C*T*T*T*T*T*T*T*T*t 3893.41 3894.25 ODN 7 A*T*G*T*G*C*T*G*C*T*A*t 3937.44 3938.28 ODN 8 T*A*A*C*A*C*G*A*T*A*C*G*C*G*A*t 5264.26 5264.75 ODN 9 T*T*T*T*t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t 6430.17 6430.15 ODN 10 t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P T*T*T*T*t 6430.17 6430.15 ODN 11 t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P T*T*T*T*t.sub.p t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t 6430.17 6430.14 ODN 12 T*T*T*T*t.sub.p t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.P t.sub.p T*T*T*T*t 6534.17 6534.38 ODN 13 T*t.sub.P t.sub.p T*t.sub.P t.sub.p t.sub.p T*t.sub.P t.sub.p t.sub.p T*t.sub.P t.sub.p t.sub.p T*t.sub.P t.sub.p t.sub.p T*t 6482.26 6482.17 ODN 14 t.sub.Pa.sub.Pg.sub.Pt.sub.Pt.sub.Pg.sub.Pa.sub.Pg.sub.Pt.sub.Pg.sub.Pa.sub.Pt.sub.PA*T*C*A*t 5343.45 5343.07 ODN 15 G*T*A*G*t.sub.Pc.sub.Pc.sub.Pt.sub.Pg.sub.Pc.sub.Pa.sub.Pa.sub.Pt.sub.Pg.sub.Pa.sub.Pt 5000.26 4999.99 ODN 16 T*G*A*t.sub.Pc.sub.Pg.sub.Pc.sub.Pt.sub.Pg.sub.Pc.sub.Pa.sub.Pa.sub.PT*G*A*t 5052.26 5052.16
[0096] N,N-Dimethylamino PMOs having oligothymidine (Table 2, ODNs 1 and 2) and all four bases (Table 2, ODNs 3-8), were synthesized using this approach and characterized by LCMS. Because it has been established that PMOs 12-16 nucleosides in length are effective inhibitors of RNA expression (either via blockage of splicing or blockage of mRNA translation), the inventors next carried out the synthesis of a 16-mer having all four bases (Table 2, ODN 8). The LCMS chromatogram of the unpurified reaction mixture showed that both the yield (10 A.sub.260 units isolated) and mass analysis of this ODN were satisfactory.
Example 3
Synthesis of PMO-DNA Chimeras
[0097] For the synthesis of PMO-DNA chimeras, 4,5-dicyanoimidazole (0.12 M and 300 s coupling time) and ETT (0.25 M and 180 s coupling time) were used for the morpholino phosphordiamidite synthons (compounds 18, 19, 20, or 21 of
[0098] Because PMO-DNA chimeras are new to the scientific community and could prove to be useful for various research projects, several were synthesized (Table 2, ODNs 9-16). Initially these chimeras were prepared as a series of 21-mer oligothymidines containing four N,N-dimethylamino PMO linkages. In these 21-mers, the morpholino diamidate linkages were placed adjacent to either the 5 or 3 ends, or near the middle of the 21mer, and at every third position throughout the oligomer (Table 2; ODNs, 9, 10, 11, 12 and 13). For these chimeras, substitution of borane with dimethylamine upon activation by iodine proceeded efficiently and analysis of the crude reaction mixtures by LCMS revealed that the expected phosphorodiamidate linkages were formed in near quantitative yields. These encouraging results were followed by the synthesis of PMO-DNA chimeras containing all four nucleobases with variable locations and number of PMO linkages (Table 2: ODNs, 14, 15, and 16). LCMS analysis and 31.sup.P NMR of the reaction mixtures demonstrated that the expected PMO-DNA chimeras were obtained in high yields with an average yield being 10-20 A260 units (from a 0.2 M synthesis cycle). These experiments also demonstrated that treatment with dimethylamine does not lead to measurable cleavage of the succinate linkage and loss of product during synthesis.
Example 4
Solid Phase Synthesis of PMOs with Amino, N-Methylamino and Morpholino Linkages
[0099] It is known that boranephosphonate linkages can be activated with iodine for displacement by a large number of nucleophiles. Therefore in addition to testing this new synthetic route by synthesizing PMO analogues having the N,N-dimethylamino-phosphorodiamidate linkage, we decided to investigate whether other amines could be used in order to generate several new PMO-DNA derivatives.
[0100] Initially, an oligothymidine 21-mer having four boranephosphoramidate morpholino linkages near the center of this oligomer was synthesized. The support containing this oligonucleotide was divided into three samples that were treated with N-methylamine, ammonia, and morpholine under iodine oxidation conditions and then purified using reverse phase column chromatography. Additionally, mixed sequence PMO-DNA chimers having all four bases and amino-phosphorodiamidate internucleotide linkages were synthesized where the positions for the diamidate linkages were located at the 5, 3, and 5/3 termini of these chimeras. The sequence and mass analysis from LCMS of these PMOs are listed in Table 3. Yields were comparable to those obtained for the N,N-dimethylamino PMO chimeras.
TABLE-US-00003 TABLE 3 LCMS Analysis of PMO-DNA Chimeras. ODN 17, 20, 21and 22: * = NH.sub.2; ODN 18: .diamond-solid. = NHMe; ODN 19: = morpholine. Phosphate linkages are denoted by p. Morpholino and 2- deoxyribonucleosides are noted as upper and lower case letters respectively. Mol wt NO ODNs Cal Obs ODN t.sub.Pt.sub.Pt.sub.Pt.sub.Pt.sub.Pt.sub.Pt.sub.Pt.sub.PT*T*T*T*t.sub.Pt.sub.Pt.sub.Pt.sub.Pt.sub.Pt.sub.Pt.sub.Pt.sub.Pt 6318.21 6318.02 17 ODN t.sub.Pt.sub.Pt.sub.Pt.sub.Pt.sub.Pt.sub.Pt.sub.Pt.sub.PT.diamond-solid.T.diamond-solid.T.diamond-solid.T.diamond-solid.t.sub.Pt.sub.Pt.sub.Pt.sub.Pt.sub.Pt.sub.Pt.sub.Pt.sub.Pt 6374.32 6374.08 18 ODN t.sub.Pt.sub.Pt.sub.Pt.sub.Pt.sub.Pt.sub.Pt.sub.Pt.sub.PTTTTt.sub.Pt.sub.Pt.sub.Pt.sub.Pt.sub.Pt.sub.Pt.sub.Pt.sub.Pt 6598.57 6598.20 19 ODN t.sub.Pa.sub.Pg.sub.Pt.sub.Pt.sub.Pg.sub.Pa.sub.Pg.sub.Pt.sub.Pg.sub.Pa.sub.Pt.sub.PA*T*C*A*t 5231.48 5230.97 20 ODN G*T*A*G*t.sub.Pc.sub.Pc.sub.Pt.sub.Pg.sub.Pc.sub.Pa.sub.Pa.sub.Pt.sub.Pg.sub.Pa.sub.Pt 4888.26 4887.89 21 ODN T*G*A*t.sub.Pc.sub.Pg.sub.Pc.sub.Pt.sub.Pg.sub.Pc.sub.Pa.sub.Pa.sub.PT*G*A*t 4884.26 4883.96 22
Example 5
Melting Temperatures of PMO-DNA Chimeras
[0101] To assess the target binding ability of the modified PMO-DNA chimeras, duplex hybridization studies were performed with 2-deoxyoligothymidines having amino, methylamino, morpholino, and dimethylamino-morpholino internucleotide linkages. PMOs 11, 17, 18 and 19 were mixed with 2-deoxyribo-, or riboadenosine-oligonucleotides that were 21-nucleotides in length, in a 1:1 ratio in a buffer (1.0 M NaCl, 10 mM sodium phosphate, pH 7.1) at an overall concentration of 1.0 M of duplex. The samples were denatured at 90 C. and cooled to 15 C. They were then heated at a rate of 1 C./min, and A.sub.260 versus time was recorded. Melting temperatures were taken as the temperature of half dissociation and were obtained from the first derivative plots (Table 4).
[0102] Melting temperature studies of RNA heteroduplexes with PMOs 11, 17, 18, and 19 showed that introduction of phosphorodiamidate internucleotide linkages stabilized the PMO:RNA duplex relative to the unmodified duplex. The trend in increased stabilization was amino>N-methylamino>N,N-dimethylamino>morpholino. When the PMO-DNA chimeras were allowed to form duplexes with a 2-deoxyriboadenosine 21mer, a similar trend was observed when compared to the Tm of the unmodified DNA.DNA duplex, except for the morpholino analogue.
TABLE-US-00004 TABLE 4 Tm Results with PMO-DNA Chimeras. PMO-DNA chimeras (ODNs 11, 17, 18, and 19), and unmodified ODN 23, (d(T).sub.21), were mixed with complementary d(A).sub.21 or r(A).sub.21 and the melting temperatures measured (Supplementary Section). T.sub.m .sup.a( C.) T.sub.m .sup.b( C.) Number Modification DNA RNA DNA RNA ODN 23 58.47 51.13 ODN 11 NMe.sub.2 58.37 52.42 0.025 0.32 ODN 17 NH.sub.2 61.37 53.37 0.75 0.56 ODN 18 NHMe 59.03 52.17 0.14 0.26 ODN 19
Example 6
RNase H1 Activity of Chimeric PMO-RNA Heteroduplexes
[0103] N,N-Dimethylamino PMO-DNA chimeras were tested for their ability to stimulate RNase H1 activity. The test systems were composed of a 5-O-fluorescein-labeled RNA and complementary N,N-dimethylamino PMO-chimeras.
[0104] Synthesis of a 5-Fluorescein PMO-DNA Chimera.
[0105] After completion of a DMT-ON synthesis of the boranephosphoramidate morpholino chimera, the ODN was conjugated with 5-Amino-Modifier C6-TFA (Glen research) using a standard DNA synthesis cycle. After carrying out the iodine oxidation reaction and desilylation of exocyclic amines, the oligonucleotide was purified using reverse phase HPLC (Buffer A: triethylammonium bicarbonate, 0.05 M, Buffer B: acetonitrile; 0-100% B in 50 mins; 55 C.; 4.0 mL/min flow rate). The purified ODN was dissolved in 1 mL of a solution of 1:1 NH.sub.4OH:CH.sub.3NH.sub.2 and heated at 65 C. for three hours to remove the trifluroacetamido group. The reaction mixture was dried and dissolved in a buffer (200 microL) containing 20 mM sodium phosphate and 0.15 M NaCl (pH 8.0) and the concentration was measured. A 20 fold molar excess of 5-(and 6-)carboxy-fluorescein succinimidyl ester (Thermo Fisher Scientific) was dissolved in DMSO and added to the ODN solution. The reaction mixture was stirred at room temperature for 1 h followed by stirring at 4 C. for a period of 3 h. The reaction mixture was diluted using 300 microL water and excess NHS-fluorescein was removed using ILLUSTRA NAP-5 Column. The analyzed PMOs were oligothymidine 14-mers with cap/gap sequences (ODNs 24-26, Table 5) having N,N-dimethylamino PMO linkages on either end and 3-7 phosphodiester linkages in the center of the analogues. Controls were complementary DNA, and 2-O-methyl RNA (which activate, and do not stimulate RNase H1 activity, respectively). All these cap/gap oligonucleotide analogues were found to activate RNA hydrolysis.
[0106] Hydrolysis of RNA Heteroduplexes with E. coli RNase H1.
[0107] Experiments with E. coli RNaseH1 (Promega) were performed using previously-described conditions (J. Am. Chem. Soc., 2003, 125:940-50). The reactions were carried out using an assay buffer of 50 mM tris-HCl (pH 8.0), 20 mM KCl, 9 mM MgCl.sub.2, 1 mM -mercaptoethanol, and 250 g/mL bovine serum albumin. An oligodeoxynucleotide or modified oligodeoxynucleotide (200 pmol) and 5-O-fluorescein-labeled, complementary oligoribonucleotide were added to the assay buffer (35 L). Following the addition of E. coli RNase H1 (3 units), reactions were carried out at 25 C. over 12 h. The reaction mixtures were diluted with an equal volume of 80% formamide gel loading buffer containing tracking dyes and analyzed by polyacrylamide gel electrophoresis (20%, 19:1 cross-linking, 7 M urea). All reactions were performed in triplicate. The developed gels were analyzed using a Molecular Dynamics Typhoon Phosphorimager.
TABLE-US-00005 TABLE 5 PMO-DNA Chimeras Used for RNaseH1 assays. Oligonucleotides containing N,N-dimethylaminophosphorodiamidate (*) and phosphate (p) linkages are shown. Morpholino and 2- deoxynucleosidesare noted by upper and lower case letters respectively. Mol wt ODN ODNs Cal Obs ODN 24 T*T*T*T*T*T.sub.pT.sub.pT.sub.pT*T*T*T*T*t 4456.79 4457.29 ODN 25 T*T*T*T*T.sub.pT.sub.pT.sub.pT.sub.pT.sub.pT*T*T*T*t 4404.81 4405.14 ODN 26 T*T*T*T.sub.pT.sub.pT.sub.pT.sub.pT.sub.pT.sub.pT.sub.pT*T*T*t 4352.91 4353.01
Example 7
Cellular Uptake
[0108] Because uncharged PMOs cannot be delivered to cells using lipid-based transfection reagents, the cellular uptake of these PMO-DNA chimeras was investigated in the presence of Dharmafect 1, a commonly used siRNA transfection reagent. A PMO-DNA chimera was synthesize (ODN 27, 5-FL-T*G*T*A*a.sub.pa.sub.pc.sub.pc.sub.pa.sub.pt.sub.pg.sub.pa.sub.pt.sub.pg.sub.pt.sub.pg.sub.pc.sub.pt.sub.pG*C*T*A*t, See Table 2 for a description of these abbreviations) where the internal, normal nucleotides were flanked at the 5- and 3-ends with N,N-dimethylamino PMO nucleotides. ODN 27 also contained a fluorescein dye (FL) joined by a six-carbon linker. HeLa cells were transfected with ODN 27 (100 nM concentration) in the presence of Dharmafect 1 with live cells and fixed cells (
[0109] Lipid Transfection as Observed by Microscope Imaging.
[0110] An ODN 27 stock solution was diluted with 200 microL OptiMEM to a final concentration of 0.1 microM ODN. In a separate Eppendorf Tube, 5.0 microL DharmaFECT 1 was diluted with 200 microL OptiMEM. The 200 microL solution of ODN 27 and the DhamaFECT 1 solution were mixed, equilibrated for 20 min, and 600 microL OptiMEM was added. Hela cells were seeded at 0.310.sup.6 cells/well on a coverslip placed in a six well plate in DMEM medium containing 10% FBS and penstrep. After 24 hours, medium was removed and the cells were washed twice (2.0 mL D-PBS/wash) before transfection at 80% confluency. D-PBS was removed from the HeLa cells, and 1.0 mL of the transfection mixture was added to each well. Cells were then incubated at 37 C. for 18 hours and washed twice (2.0 mL D-PBS/wash). Cells were covered with 1.0 mL of 10% neutral buffer formalin for 15 mins. The formalin solution was removed and the cells were covered with 3.0 mL DPBS for 10 min at RT. The coverslips were removed from the wells and mounted upside down on coverslides using Flouromount-G with DAPI as mounting media and observed using an inverted microscope (OlympuslX 81) equipped with a Hamamatsu C4742-95 CCD and CoolSNAP ES digital camera.
[0111] The transfection was dose dependent as an increased fluorescent signal was observed when cells were incubated with 100 nM of ODN 27. The fluorescence appears to be distributed primarily in the nucleus although there is also evidence of cytoplasmic distribution without the common punctuated structures found for many analogues.
Example 8
Synthesis of Phosphoramidite Monomers for Thiomorpholino Synthesis
[0112] The general procedure for the synthesis of phosphoramidite monomers (compounds 19, 20, 21, and 22 of
5-dimethoxytrityl-morpholinothymidine-3-N-cyanoethyl-N,N diisopropyl phosphoradiamidite (compound 19 of
N.sup.4-benzoyl-5-dimethoxytrityl-morpholinocytidine-3-N-cyanoethyl-N,N-diisopropyl phosphoradiamidite (compound 20 of
N.sup.6-benzoyl-5-dimethoxytrityl-morpholinoadenosine-3-N-cyanoethyl-N,N-diisopropyl phosphoradiamidite (compound 21 of
N.sup.2-isobutyryl-5-dimethoxytrityl-morpholinoguanosine-3-N-cyanoethyl-N,N-diisopropyl phosphoradiamidite (compound 22 of
[0113] Solid Phase Synthesis: The procedure used to synthesize TMO and TMO-DNA chimeras is described in the synthesis scheme depicted in
[0114] Automated TMO Synthesis: Syntheses were carried out on an ABI 394 Synthesizer. All syntheses were performed at a 1.0 mol scale using a 5-DMTr-2-OMe-ribouridine joined to a CPG solid support via a succinate linkage. For the synthesis of thiomorpholino oligonucleotides, the phosphordiamidites (19, 20, 21, or 22; 0.1 M) were dissolved in anhydrous CH.sub.3CN. The standard 1.0 mole synthesis cycle was used with an increase in coupling time to 300 s. Following oxidation and capping, detritylations were carried out using a 3% solution of trichloroacetic acid in dichloromethane. A stepwise description of the synthesis cycle is described in Table 6. All syntheses were carried out with DMT ON. Following synthesis, resins were transferred to a 1.5 mL screw cap vial and treated with 1.0 mL NH.sub.4OH (37%) for 18 h at 55 C.
TABLE-US-00006 TABLE 6 Chemical Steps used to Prepare Thiomorpholino Oligonucleotides. Reactions Wash/reagents/solvents Time (s) Detritylation 3% trichloroacetic acid in dichloromethane Flow 90 s Condensation 0.1M phosphordiamidite 19, 20, 21, or 22 Wait 300 s (in CH.sub.3CN) + Activator (0.12M dicyanoimidazole in CH.sub.3CN) or 0.1M phosphoramidite 23, 24, 25, or 26 in Wait 180 s CH.sub.3CN + Activator (0.25M ethylthio tetrazole in CH.sub.3CN) Sulfurization 3-((N,N-dimethylaminomethylidene)amino)- Flow 15 s, 3H-1,2,4-dithiazole-5- wait 90 s thione in pyridine, acetonitrile; 3:2 Wash Anhydrous CH.sub.3CN Flow 10 s Capping Cap A (THF/Pyridine/Ac.sub.2O) + Flow 10 s, Cap B (16% 1-methyl imidazole in THF) wait 5 s Wash Anhydrous CH.sub.3CN Flow 10 s Wash Anhydrous CH.sub.2Cl.sub.2 Flow 25 s
[0115] The RP-HPLC purification protocol: A linear gradient of 0 to 40% B over 301.0 min at a flow rate of 1.0 Room Temperature mL/min; buffer A: 50 mM TEAB, pH 8.5; buffer B: acetonitrile 40%, Room Temperature. Column specifications:)(Bridge Oligonucleotide BEH C18 Prep Column, 130 , 2.5 m, 10 mm50 mm. This purification step yields the product as a broad peak due to the presence of multiple chiral phosphorus centers.
[0116] LC-MS analyses were carried out on an Agilent 6530 series Q-TOF LC/MS spectrometer. A waters ACQUITY UPLC BEH C18, 1.7 m, 2.1100 nm column was used with a gradient of 0-100% of buffer B in 50 min with a flow rate of 0.2 mL/min (Buffer A was 1:380:10:10.4 mixture of triethylamine:water:methanol:hexafluoro-2-propanol and Buffer B was 1:370:20:10.4 mixture of triethylamine:methanol:water:hexafluoro-2-propanol).
[0117] The foregoing examples of the present invention have been presented for purposes of illustration and description. Furthermore, these examples are not intended to limit the invention to the form disclosed herein. Consequently, variations and modifications commensurate with the teachings of the description of the invention, and the skill or knowledge of the relevant art, are within the scope of the present invention. The specific embodiments described in the examples provided herein are intended to further explain the best mode known for practicing the invention and to enable others skilled in the art to utilize the invention in such, or other, embodiments and with various modifications required by the particular applications or uses of the present invention. It is intended that the appended claims be construed to include alternative embodiments to the extent permitted by the prior art.
[0118] To the extent that the appended claims have been drafted without multiple dependencies, this has been done only to accommodate formal requirements in jurisdictions which do not allow such multiple dependencies. It should be noted that all possible combinations of features which would be implied by rendering the claims multiply dependent are explicitly envisaged and should be considered part of the invention.