Rep protein for use in a diagnostic assay

Abstract

The present invention concerns a DNA-replication-associated (Rep) protein comprising an amino acid sequence as depicted in SEQ ID NO: 11 or 12; (b) a fragment of SEQ ID NOs:11 or 12 which is capable of binding an anti-Rep antibody specific for a protein having the amino acid sequence of SEQ ID NOs: 11 or 12; or (c) an amino acid sequence having a 90% or more homology to the amino acid sequence of (a) or (b) and is capable of binding an anti-Rep antibody specific for a protein having an amino acid sequence of SEQ ID NOs:11 or 12. The present invention further concerns a method of diagnosing MS or a predisposition for MS and a kit for use in such methods.

Claims

1. A DNA-replication-associated (Rep) protein comprising the amino acid sequence of SEQ ID NOs: 11 or 12.

2. A method of diagnosing multiple sclerosis (MS) in a subject comprising the steps of (a) incubating a sample from a subject with a Rep protein as defined in claim 1; (b) detecting the amount of antibodies in the sample from the subject forming an immunological complex with the Rep protein; and (c) correlating the amount of antibody bound to Rep protein in the sample from the subject, as compared to an amount in a control sample, for diagnosing MS.

3. The method of claim 2, wherein in step (a) the Rep protein is immobilized followed by incubating the immobilized Rep protein with the sample from the subject.

4. The method of claim 2, wherein in step (a) the Rep protein is expressed in cells followed by incubating the cells with the sample from the subject.

5. The method of claim 2, wherein in step (b) the amount of antibodies forming an immunological complex with Rep protein is quantified by a detecting binding agent coupled to a signal generating compound.

6. The method of claim 2, wherein in step (a), the antibodies in the sample from the subject are immobilized prior to incubating with a defined amount of the Rep protein.

7. The method of claim 2, wherein the sample from the subject is a serum or a plasma sample.

8. The method of claim 2, wherein MS or a predisposition for MS is indicated by an increased amount of anti-Rep antibodies in the subject's sample of at least 2 fold as compared to a control sample.

9. A kit for use in the diagnosis of MS comprising: (a) a Rep protein, wherein the Rep protein comprises the amino acid sequence of SEQ ID NO:11 or 12; (b) an anti-human antibody coupled to a detectable label and capable of binding to anti-Rep antibody with a specificity for a protein having the amino acid sequence of SEQ ID NO: 11 or 12, and (c) a solid matrix suitable for immobilizing a Rep protein according to (a).

10. The kit according to claim 9 for use in an assay selected from the group consisting of enzyme-linked immunosorbent assay (ELISA), radioimmunoassay (RIA), enzyme immune assay (EIA), fluorescence immunoassay (FIA), luminescence immunoassay (LIA) and strip assay.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 Rep protein was overexpressed by transient transfection of HEK293TT with a pcDNA3.1() plasmid coding for either MSBI1 Rep wild type (WT) or mutant MSBI1 Rep 27/154E for 72 hours. Cells were trypsinized, washed in PBS and sonified in lysis buffer (50 mM Tris pH 7.6, 150 mM NaCl, 1.5% Triton X-100, 5 mM imidazole, 5 mM betamercaptoethanol, 1 proteinase inhibitor mix). After incubation (30 min, 4 C.) and centrifugation (30 min, 10,000 g, 4 C.) non-denaturing protein purification was carried out by binding to protein to 1 ml equilibrated Ni-NTA beads (Clontech), washing with 10 column volumes washing buffer (lysis buffer containing 55 mM imidazole) and elution (lysis buffer containing 300 mM imidazole). After protein quantification by NanoDrop and Bradford, equal amounts of protein (500 ng per lane) were boiled in Lammli buffer with (reduced) or without (oxidized) 5 mM beta mercaptoethanol and analyzed by SDS-PAGE and western blotting with anti-Rep antibodies.

(2) FIG. 2 Rep protein was purified under non-denaturing conditions as above. 2000 ng Rep protein were subjected to BN-PAGE (Serva) and stained either by anti-Rep immunodetection or protein silver staining.

(3) FIG. 3 Rep protein was purified from E. coli under denaturing conditions (protocol see below). Either 2 g (western blot) or 5 g (Coomassie staining) of purified MSBI1 Rep wt or mutant MSBI1 Rep 27/154E were characterized by anti-Rep immunodetection or Coomassie protein staining following SDS-PAGE.

(4) FIG. 4 Rep protein was purified from E. coli under denaturing conditions (protocol see below). 5 g MSBI1 Rep wt or mutant MSBI1 Rep 27/154E were used for BN-PAGE and anti-Rep immunodetection.

(5) FIG. 5 ELISA plates (Maxisorp, Thermo Fisher Scientific) were coated either with purified denatured MSBI1 Rep wt or mutant MSBI1 Rep 27/154E at 4 C. overnight in 1:1 dilution of 1PBS/8 M urea (200 ng protein per well) in triplicates. Blocking was performed in different assay buffers (casein, superblock, 1% BSA in PBS) for 2 h at RT. The coated protein was quantified with a pool of three mouse monoclonal anti-Rep antibodies (1:500 dilution, with epitopes in the N-, central-, and C-terminal Rep domain) as primary antibodies followed by incubation with an HRP-coupled goat anti-mouse secondary antibody (1:5000 dilution, each 1 h at 37 C., washing with PBS 0.1% Tween, TMB ELISA substrate from Thermo Fisher Scientific, readout at 450 nm). Raw signal intensities are shown.

(6) FIG. 6 ELISA plates (Maxisorp, Thermo Fisher Scientific) were coated either with purified denatured MSBI1 Rep wt or mutant MSBI1 Rep 27/154E at 4 C. overnight in 1:1 dilution of 1PBS/8 M urea (200 ng protein per well). Blocking was performed in superblock assay buffer for 2 h at RT. Serum incubation (1:500 in superblock buffer) was performed for 1 h at 37 C. Rep-bound human IgG antibodies were quantified with an HRP-coupled goat anti-human secondary antibody (1:5000 dilution, 1 h at 37 C.) in duplicate analysis (washing with PBS 0.1% Tween, TMB ELISA substrate from Thermo Fisher Scientific, readout at 450 nm, signal normalized to BSA control).

DETAIL DESCRIPTION OF THE INVENTION

(7) The invention provides mutant Rep proteins and diagnostic screening assays for the presence of anti-Rep antibodies as pathogenic markers. Samples containing increased amounts of anti-Rep antibodies indicate that the corresponding subject was definitely exposed to Rep-related protein or himself expressed Rep protein during a time period long enough to induce a Rep protein specific immune response. With such screening assays a diagnosis, prognosis and monitoring of MS based on the quantification of anti-Rep antibodies can be conducted.

(8) Rep protein as used herein refers to a DNA-replication-associated protein (RepB). The Rep protein comprises DNA binding activity and could be essential for initiation of replication of episomal/viral DNA molecules. In general Rep protein refers to a Rep protein from the group of the Small Sphinx Genome (Whitley et al., 2014). In particular, the Rep protein is a synthesized genome-encoded Rep protein MSBI1 Rep 27/154E and a MSBI2 genome-encoded Rep 27/154E protein. Preferably, the synthesized MSBI1 Rep protein has the amino acid sequence as depicted in SEQ ID NO:11 and is derived from MSBI1.176 deposited in the EMBL databank under the acc. no. LK931491 which has the amino acid sequence as depicted in SEQ ID NO:1, or the synthesized Rep protein has the amino acid sequence as depicted in SEQ ID NO:12 and is derived from MSBI2.176 deposited in the EMBL databank under the acc. no. LK931492 which has the amino acid sequence as depicted in SEQ ID NO:8.

(9) In a particular preferred embodiment the Rep protein comprises a N-terminal region conserved among small Sphinx genomes consisting essentially of amino acids from 1 to 229 of SEQ ID NO: 11 or 12 and a C-terminal variable region specific for MSBI1.176 consisting essentially from amino acids 230 to 324 of SEQ ID NO: 11, or C-terminal variable region specific for MSBI2.176 consisting essentially from amino acids 230 to 324 of SEQ ID NO: 12. The N-terminal conserved region comprises a putative, first DNA binding domain consisting essentially of amino acids from 1 to 136 of SEQ ID NOs: 1, 8, 11 and 12 and a second putative DNA binding domain consisting essentially of amino acids from 137 to 229 of SEQ ID NOs:1, 8, 11 and 12.

(10) Rep protein also encompasses fragments and variants of the protein which are capable of binding an anti-Rep antibody specific for Rep protein having the amino acid sequence of SEQ ID NO: 11 or 12. Preferably, such a fragment is an immunogenic fragment of the protein having the amino acid sequence of SEQ ID NO: 11 or 12 which encompasses at least one epitope for an anti-Rep protein antibody against the Rep protein of SEQ ID NO:11 or SEQ ID NO:12 and, preferably, comprises at least 7, 8, 9, 10, 15, 20, 25 or 50 contiguous amino acids. In particular embodiments the fragment comprises or consists essentially of a domain of the Rep protein, for example, the N-terminal conserved region, the C-terminal variable region, the first or second DNA binding domain. A variant of the protein with SEQ ID NO:11 or SEQ ID NO:12 comprises one or more amino acid deletions, substitutions or additions compared to SEQ ID NO:11 or SEQ ID No. 12 and has a homology of at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% to the amino acid sequence of SEQ ID NO:11 or SEQ ID NO: 12, wherein the variant is capable of binding an anti-Rep antibody specific for a Rep protein having the amino acid sequence of SEQ ID NO:11 or SEQ ID NO:12. Included within the definition of variant are, for example, polypeptides containing one or more analogues of an amino acid (including, for example, unnatural amino acids, peptide nucleic acid (PNA), etc.), polypeptides with substituted linkages, as well as other modifications known in the art, both naturally occurring and non-naturally occurring. The term Rep protein includes fusion proteins with a heterologous amino acid sequence, with a leader sequence or with a Tag-sequence and the like. For example the Rep protein may be fused to a Tag-sequence, for example, selected from the group consisting of His.sub.6-Tag (SEQ ID NO:4), T7-Tag (SEQ ID NO:5), FLAG-Tag (SEQ ID NO:6) and Strep-II-Tag (SEQ ID NO:7).

(11) The synthesized MSBI1 Rep protein (MSBI1 Rep 27/154E) or MSBI2 Rep protein (MSBI2 Rep 27/154E) of the invention, including the Rep fragments and Rep variants as defined above, can be prepared by classical chemical synthesis. The synthesis can be carried out in homogeneous solution or in solid phase. The polypeptides according to this invention can also be prepared by means of recombinant DNA techniques. For example, MSBI1 Rep 27/154E was engineered in which the aggregation potential of two amino acid sequences between residues 25-31 (LLILLAII) and residues 151-155 (LLICW) was minimized by two single point mutations. The basis for the cloning was a MSBI1 Rep DNA sequence which was codon-optimized for Rep expression in the human system encoding the original MSBI1 Rep primary amino acid sequence. The nucleotides coding for amino acid 27 (L, Leucine, DNA codon CTA) as well as the nucleotides coding for amino acid 154 (C, Cysteine, DNA codon TGT) were substituted by nucleotides coding for the amino acid glutamic acid (E, DNA codon GAG) equaling the final DNA sequence SEQ ID NO: 11. The net aggregation potential of this Rep double mutant was minimized to a score of 141 being in the range of non-aggregation prone proteins.

(12) As shown in the Examples (FIG. 2, 3), the Rep 27/154E mutant showed a significant reduction (>50%) of Rep oligomers and larger aggregates when compared with the wild-type Rep protein. Western blotting also showed significantly less Rep oligomers as well as less high molecular weight aggregates (FIG. 4). An additional species of most obviously monomeric Rep protein was detected under native PAGE conditions only for the Rep mutant. Clearly, the intensity of high molecular weight aggregates is significantly reduced for the 27/154E Rep double mutant. In general, the presence of Rep aggregates is higher for proteins which were purified under non-denaturing conditions. Anyways, also proteins purified and stored under denaturing conditions show very strong aggregation, which is significantly reduced for the Rep double mutant. This is of special interest, as ELISA experimental setups rely and renaturation of the surface-bound protein antigens, because antibody antigen binding necessitates native conditions.

(13) The wild type Rep proteins can be prepared by classical chemical synthesis. The synthesis can be carried out in homogeneous solution or in solid phase. The polypeptides according to this invention can also be prepared by means of recombinant DNA techniques. An example for producing and purification of a wild type Rep protein is shown in Example 1.

(14) Subject as used herein refers to a mammalian individual or patient, including murines, cattle, for example bovines, simians and humans. Preferably, subject is a human patient.

(15) Sample as used herein refers to a biological sample encompassing liquid and solid samples. Liquid samples encompass blood liquids such as, for example, sera or plasma and cerebrospinal fluid (CSF). Solid samples encompass tissue samples such as tissue cultures or biopsy specimen.

(16) Correlates with as used herein refers to an amount, i.e. level or titer, of anti-Rep antibodies and Rep protein, respectively, with a significant correlation with a disease status of, for example, MS. The correlation is determined by detecting the extent of difference in the amount present in a sample from a subject to be tested and a control sample. Control sample means a single sample or an average of various, i.e. more than two, control samples. The control is taken from a healthy individual who has not been diagnosed for MS. Alternatively, the correlation may be theoretically determined by detecting the extent of difference in the amount present in a sample for a subject to be tested with a predetermined cut-off value. A cut-off value is a reference value with statistically significant separation between different disease status, e.g. between healthy and diseased status. The cut-off value can be determined by statistical analysis of a sufficiently large panel of test samples from patients with disease history and samples from healthy test group by statistical tests known in the art.

(17) In certain embodiments a diagnosis, for example of MS, is indicated by an at least 2 fold, 3 fold, 4 fold, 5 fold, 10 fold, 50 fold, 100 fold, 500 fold or 1000 fold increased amount of protein, i.e Rep protein and anti-Rep-antibodies, respectively, in the sample from the subject as compared to a control sample.

(18) Anti-Rep antibody as used herein refers to an antibody binding at a detectable level to Rep protein in the methods of the invention which affinity is more strongly to the Rep protein of the invention than to a non-Rep protein. Preferably, the antigen affinity for Rep protein is at least 2 fold larger than background binding. In particular the anti-Rep antibody is specific for the MSBI1 Rep having the amino acid sequence of SEQ ID NO:1 or 11 or MSBI2 Rep having the amino acid sequence of SEQ ID No: 8 or 12. In particular embodiments the antibody is cross-specific for MSBI1 Rep or MSBI2 Rep.

(19) A common feature of all assays is that the Rep protein is contacted with a sample suspected of containing anti-Rep protein antibodies under conditions that permit the Rep protein to bind to any such antibody present in the sample. Such conditions will typically be physiologic temperature, pH and ionic strength using an excess of Rep protein. The incubation of the Rep protein with the sample is followed by detection of immune complexes comprised of the antigen. In certain embodiments either the Rep protein is coupled to a signal generating compound, e.g. detectable label, or an additional binding agent, e.g. secondary anti-human antibody, coupled to a signal generating compound is used for detecting the immune complex.

(20) Anti-Rep antibodies can be detected and quantified in assays based on Rep protein as protein antigen, which serves as target for the mammalian, e.g. human, antibodies suspected in the sample. Preferably, the Rep protein is purified (e.g. see Example 1) and the samples can be, for example, serum or plasma samples. The methods include immobilization of Rep protein on a matrix followed by incubation of the immobilized Rep protein with the samples. Finally, the Rep-bound antibodies of the formed immunological complex between Rep protein and antibodies of the samples are quantified by a detection binding agent coupled to a signal generating compound, e.g. secondary HRP-(horseradish-peroxidase)-coupled detection antibody allowing for HRP-substrate based quantification. This signal generating compound or label is in itself detectable or may be reacted with an additional compound to generate a detectable product.

(21) In other embodiments anti-Rep antibodies are indirectly quantified in that first the antibodies of the sample are immobilized on a matrix, followed by incubation with a defined amount of Rep protein, wherein the anti-Rep antibodies immobilized and present on the matrix capture the Rep protein from the protein-sample liquid mixture, followed by quantification of the bound Rep protein.

(22) In other embodiments Rep protein can be expressed in cells and these cells are incubated with the sample. Thereafter, anti-Rep antibodies from the sample bound to the Rep protein expressed by cells are detected and quantified.

(23) Design of the immunoassay is subject to a great deal of variation, and many formats are known in the art. Protocols may, for example, use solid supports, or immunoprecipitation. Most assays involve the use of binding agents coupled to signal generating compounds, for example labelled antibody or labelled Rep protein; the labels may be, for example, enzymatic, fluorescent, chemiluminescent, radioactive, or dye molecules. Assays which amplify the signals from the immune complex are also known; examples of which are assays which utilize biotin and avidin or streptavidin, and enzyme-labeled and mediated immunoassays, such as ELISA assays.

(24) The immunoassay may be in a heterogeneous or in a homogeneous format, and of a standard or competitive type. In a heterogeneous format, the polypeptide (Rep protein or anti-Rep antibody) is typically bound to a solid matrix or support or carrier to facilitate separation of the sample from the polypeptide after incubation. Examples of solid supports that can be used are nitrocellulose (e. g., in membrane or microtiter well form), polyvinyl chloride (e. g., in sheets or microtiter wells), polystyrene latex (e. g., in beads or microtiter plates, polyvinylidine fluoride (known as Immunolon), diazotized paper, nylon membranes, activated beads, and Protein A beads. The solid support containing the antigenic polypeptides is typically washed after separating it from the test sample, and prior to detection of bound anti-Rep antibodies. Both standard and competitive formats are known in the art.

(25) In a homogeneous format, the test sample is incubated with the Rep protein in solution. For example, it may be under conditions that will precipitate any Rep protein-antibody complexes which are formed. Both standard and competitive formats for these assays are known in the art.

(26) In a standard format, the amount of anti-Rep antibodies in the antibody-Rep protein complexes is directly monitored. This may be accomplished by determining whether (labelled) anti-xenogeneic (e. g. anti-human) antibodies which recognize an epitope on anti-Rep antibodies will bind due to complex formation. In a competitive format, the amount of anti-Rep antibodies in the sample is deduced by monitoring the competitive effect on the binding of a known amount of labelled antibody (or other competing ligand) in the complex.

(27) Complexes formed comprising anti-Rep antibody (or in the case of competitive assays, the amount of competing antibody) are detected by any of a number of known techniques, depending on the format. For example, unlabeled anti-Rep antibodies in the complex may be detected using a conjugate of anti-xenogeneic Ig complexed with a label (e. g. an enzyme label, such as, for example, HRP).

(28) In an immunoprecipitation or agglutination assay format the reaction between the Rep protein and the anti-Rep antibody forms a network that precipitates from the solution or suspension and forms a visible layer or film of precipitate. If no anti-Rep antibody is present in the sample, no visible precipitate is formed.

(29) The solid phase selected can include polymeric or glass beads, nitrocellulose, microparticles, microwells of a reaction tray, test tubes and magnetic beads. The signal generating compound can include an enzyme, a luminescent compound, a chromogen, a radioactive element and a chemiluminescent compound. Examples of enzymes include alkaline phosphatase, horseradish peroxidase (HRP) and beta-galactosidase. Examples of enhancer compounds include biotin, anti-biotin and avidin. Examples of enhancer compounds binding members include biotin, anti-biotin and avidin.

(30) In further embodiments the invention provides methods wherein an increased amount of Rep protein in a sample correlates with a diagnosis or predisposition of a neurodegenerative disease, for example MS, or is used for monitoring the disease, for example MS, or monitoring the treatment of the disease, for example MS. In such embodiments the Rep protein in the sample is detected by anti-Rep antibodies.

(31) Such methods comprise the steps of (a) detecting the amount of Rep protein in a sample from a subject by anti-Rep antibodies; and (b) correlating the amount of Rep protein detected in the sample from a subject in step (a) as compared to an amount in a control sample with a diagnosis of a neurodegenerative disease, for example MS.

(32) Examples for assays which can be used in such methods for the detection of Rep protein in serum or plasma samples include, but are not limited to immunoprecipitation, immunofluorescence, dot blotting and Western Blot.

(33) For example, a serum sample may be incubated with anti-Rep protein antibodies to capture the Rep protein in the sample, followed by a step of immunoprecipitation of Rep protein and, thereafter, a step of detection by SDS-PAGE and Western Blot.

(34) In a further example, a dot blot membrane may be incubated with serum, followed by the step of a SDS-PAGE and Western Blot.

(35) In a further example, serum dilutions of the sample are loaded on SDS-Page followed by a Western Blot.

(36) In further embodiments Rep protein is detected in tissue samples by immunohistochemical methods or immunofluorescence microscopy.

(37) In certain embodiments anti-Rep antibodies are used for the detection or capturing of the Rep protein in the sample.

(38) The term antibody, preferably, relates to antibodies which consist essentially of pooled polyclonal antibodies with different epitopic specificities, as well as distinct monoclonal antibody preparations. As used herein, the term antibody (Ab) or monoclonal antibody (Mab) is meant to include intact immunoglobulin molecules as well as antibody fragments (such as, for example, Fab and F(ab)2 fragments) which are capable of specifically binding to Rep protein. Fab and F(ab)2 fragments lack the Fc fragment of intact antibody, clear more rapidly from the circulation, and may have less non-specific tissue binding than an intact antibody. Thus, these fragments are preferred, as well as the products of a FAB or other immunoglobulin expression library. Moreover, antibodies useful for the purposes of the present invention include chimerical, single chain, multifunctional (e.g. bispecific) and humanized antibodies or human antibodies.

(39) In certain embodiments the antibody or antigen binding fragment thereof is coupled to a signal generating compound, e.g., carries a detectable label. The antibody/fragment can be directly or indirectly detectably labeled, for example, with a radioisotope, a fluorescent compound, a bioluminescent compound, a chemiluminescent compound, a metal chelator or an enzyme. Those of ordinary skill in the art will know of other suitable labels for binding to the antibody, or will be able to ascertain such, using routine experimentation.

(40) As shown in the Example part, the newly engineered double Rep mutant shows a comparable ELISA coating performance when compared to the wild-type Rep protein. Additionally, the reactivity of Rep-reactive antibodies in human MS sera was increased by about 40% on average when using the 27/154E Rep double mutant as antigen when compared to wild-type Rep in ELISA assays (FIG. 6.)

(41) The inventors have also raised (generated) anti-Rep antibodies against a Rep protein having the amino acid sequence of SEQ ID NO:1 or SEQ ID NO:8 or a fragment thereof by methods well known to those skilled in the art. These anti-Rep antibodies are used for binding to several or all kinds of Rep proteins from the group of the Small Sphinx Genome (anti-Small-Sphinx-like Rep antibody or anti-SSLRep antibody). Such anti-SSLRep antibody binds to an epitope within the conserved N-terminal region of the Rep protein from amino acids 1 to 229 of SEQ ID NO:1. Anti-Rep antibodies of the anti-SSLRep type are used which bind to an epitope within SEQ ID NO:2 (amino acids 32-49 of SEQ ID NO:1) or SEQ ID NO:3 (amino acids 197-216 of SEQ ID NO:1). The peptide fragments of SEQ ID NO:2 and SEQ ID NO:3 are highly conserved among the Rep proteins from the Small Sphinx Genome group and appear to be exposed due to their hydrophilic character. Anti-Rep antibodies of the anti-SSLRep type may be produced by immunization, for example of mice or guinea pig, by peptides consisting essentially of the amino acid sequences as depicted in SEQ ID NOs:2 or 3; or by other immunogenic fragments, preferably comprising at least 8-15 amino acids, derived from the conserved N-terminal Rep protein region from amino acids 1 to 229 of SEQ ID NO:1.

(42) Such antibodies have been produced, for example, by immunization of a mammal such as mice or guinea pig with a full-length Rep protein having the amino acid sequence of SEQ ID NO:1.

(43) These anti-Rep antibodies are capable of detecting Rep protein up to ranges from picogramm to femtogramm in different kinds of body liquids such as, for example, blood, serum, spinal fluid or cerebral fluid.

(44) Either a specific kind of anti-Rep antibody or a pool of two or more different kinds of anti-Rep antibodies may be used. If a pool of different kinds of anti-Rep antibodies is used, the anti-Rep antibody pool may comprise different anti-Rep antibodies binding to different epitopes within different domains of the Rep protein, e.g. first DNA binding domain (e.g. aa 1-136 of SEQ ID NO:1), second DNA binding domain (e.g. aa 137-229 of SEQ ID NO:2) and/or variable domain (e.g. aa 230-324 of SEQ ID NO:1), in particular, of MSBI1 Rep protein (SEQ ID NO:1).

(45) In view of the only two single point mutations in the two DNA binding domains and the maintenance of the same sequence in the variable domains, these antibodies also recognize the mutant proteins of SEQ ID Nos. 11 and 12.

(46) For the detection of a Rep protein by anti-Rep antibodies methods such as, for example, Western Blot, immunofluorescence microscopy or immunohistochemical methods may be applied.

(47) Anti-Rep antibodies are capable of detecting a Rep protein at certain cellular localizations. For instance the anti-Rep antibody may detect the Rep protein in cytoplasma, nuclear membrane and nucleus or detect speckles in cytoplasma. Examples of such group of anti-Rep antibodies are shown in Table 1:

(48) TABLE-US-00001 Antibody RepProtein DSMZ Group Localization Specificity Antibody deposit Group A cytoplasm + MSBI1 + ABO1 523-1-1 DSM nuclear small- ACC3327 membrane sphinx-like (+nucleus) Group B speckles in MSBI1 + ABO2 304-4-1 DSM cytoplasm small- ACC3328 sphinx-like Group C cytoplasm + MSBI1 MSBIl 381-6-2 DSM nuclear specific ACC3329 membrane (+nucleus) Group D speckles in MSBI1 Dl: MSBI1 DSM cytoplasm specific 961-2-2 ACC3330 D2: MSBI1 761-5-1

(49) Anti-Rep antibodies of group A have an epitope within the amino acid sequence depicted in SEQ ID NO:3 (aa 198-217 of SEQ ID NO:1) and are capable of detecting MSBI1 Rep and Rep proteins comprising this conserved epitope of the Small Sphinx Genome group (e.g. MSBI2, CMI1, CMI4). In immunofluorescence assays such anti-Rep antibodies detect a specific Rep localization pattern, wherein the main localization is homogeneously distributed over the cytoplasm and nuclear membrane; and additional weak and homogeneously distributed localization is seen in the nucleus. An example of such a group A antibody is antibody AB01 523-1-1 (DSM ACC3327) which was employed in the examples as group A antibody.

(50) Anti-Rep antibodies of group B have an epitope within the amino acid sequence depicted in SEQ ID NO:2 (aa 33-50 of SEQ ID NO:1) and are capable of detecting MSBI1 Rep and Rep proteins comprising this conserved epitope of the Small Sphinx Genome group (e.g. MSBI2, CMI1, CMI4). In immunofluorescence assays such anti-Rep antibodies detect specifically speckles (cytoplasmatic aggregations) of the Rep protein (often in the periphery of the nuclear membrane). An example of such a group B antibody is the antibody designated as AB02 304-4-1 (DSM ACC3328) which was employed in the examples as group B antibody.

(51) Anti-Rep antibodies of group C detect specifically a structural epitope of MSBI1 (SEQ ID NO:1). In immunofluorescence assays such anti-Rep antibodies detect a specific Rep localization pattern, wherein the main localization is homogeneously distributed over the cytoplasm and nuclear membrane; and additional weak and homogeneously distributed localization is seen in the nucleus. An example of such a group C antibody is antibody MSBI1 381-6-2 (DSM ACC3329) which was employed in the examples as group C antibody.

(52) Anti-Rep antibodies of group D detect specifically a structural epitope of MSBI1 (SEQ ID NO:1), where antibody MSBI1 961-2-2 designated as D1 detects an epitope depicted in SEQ ID NO:9 (aa 281-287) in the C-terminal domain of MSBI1. Antibody MSBI1 761-5-1 (DSM ACC3328) designated as D2 detects a 3D structural epitope of MSBI1 which is exclusively accessible under in vivo conditions and is not accessible in Western Blots. In immunofluorescence assays such anti-Rep antibodies detect specifically speckles (cytoplasmatic aggregations) of the Rep protein (often in the periphery of the nuclear membrane.

(53) In certain embodiments the anti-Rep antibodies of groups A, B, C or D; or a combination of anti-Rep antibodies of at least two different groups A, B, C or D are used to determine the kind of Rep protein localization in a probe and if such a Rep protein localization correlates with a pathogen function. For instance, if speckles are present. In certain embodiments, i.e., methods or kits of the invention, at least one anti-Rep antibody selected from groups A and B is combined with at least one anti-Rep antibody selected from groups C and D. In particular embodiments, i.e., methods or kits of the invention, an anti-Rep antibody of group A is combined with at least one further anti-Rep antibody selected from the groups B, C, and D. For instance, an anti-Rep antibody of group A may be combined with further anti-Rep antibodies of groups C and D. Such combinations of anti-Rep antibodies of different groups increases the distinctness of the diagnostic assessment, in particular for the diagnosis of MS.

(54) The following antibodies were deposited with the Deutsche Sammlung fr Mikroorganismen and Zellkulturen (DSMZ) [German Collection of Microorganisms and Cell Cultures] on Sep. 28, 2017:

(55) antibody AB01 523-1-1 under DSM ACC3327;

(56) antibody AB02 304-4-1 under DSM ACC3328;

(57) antibody MSBI1 381-6-2 under DSM ACC3329; and

(58) antibody MSBI1 761-5-1 under DSM ACC3330.

(59) Antibody MSBI1 961-2-2 has been deposited with DSMZ on Oct. 6, 2017.

(60) In a preferred embodiment the anti-Rep antibodies of groups A, B, C or D; or a combination of anti-Rep antibodies of at least two different groups A, B, C or D are used to determine the synthesized MSBI1 Rep genome encoded Rep protein (MSBI1 Rep 27/154E or MSBI2 Rep 27/154E)).

(61) In further embodiments a kit for use in the diagnosis of MS is provided. The kit may include material for detecting anti-Rep antibodies and/or Rep protein together with instructions for use of the materials in assays for the diagnosis of MS. The kit may comprise one or more of the following components: a biomarker according to the invention, i.e. Rep protein and anti-Rep antibodies, respectively; a signal generating compound, a solid matrix for attaching a capturing agent, a diluent for the samples, a wash buffer. Signal generating compound refers to a detectable label which is either coupled to an additional binding agent capable of binding to the biomarker of the invention or directly coupled with the biomarker of the invention.

(62) The invention is further illustrated by, but not limited to, the following examples:

EXAMPLES

Example 1

(63) MSBI1 Rep Protein Purification

(64) A nucleotide acid molecule encoding full-length Rep open reading frame (ORF) identified within the MSBI1 genome is cloned into an expression plasmid (pEXP5-CT, Invitrogen) enabling protein expression based on an E. coli high yield cell free in vitro translation system (Expressway Cell-Free E. coli Expression System, Invitrogen). The synthesized Rep protein having the amino acid sequence of SEQ ID NO:1 within the in vitro translation reaction is denaturated by adding 20 reaction volumes 8 M urea sample buffer pH 8.0 containing 100 mM NaH2PO4, 10 mM Tris HCl, pH 8.0, 5 mM imidazole. The Rep protein is subsequently purified under denaturating conditions (20 mM imidazole for washing and 300 mM imidazole for protein elution) based on a C-terminal His6-tag fused to the Rep protein. Quality of purification is determined by Coomassie protein staining and Western Blotting with anti-Rep protein antibodies. The Rep protein purity is densitometrically calculated and greater 95%. The purified protein is either directly used for ELISA-based serum screening or subjected to SDS-Page followed by transfer blotting onto nitrocellulose membranes for serum incubation of 1D-size-resolved Rep protein membrane stripes.

Example 2

(65) A. Characterization of Wildtype or Mutant Rep Protein Under Denaturing Conditions Using SDS-PAGE and Western Blotting

(66) The properties of the purified Rep antigens (wildtype and mutant Rep) were characterized by different sets of experiments. Rep protein, which was purified under non-denaturing (native) conditions from human HEK293TT cell line, showed significantly less levels of Rep oligomers (100 kDa band) and less heavy molecular weight aggregates for the single C154E and double 27/154E mutants when compared with the wildtype both under reducing and oxidizing sample loading conditions when subjected to SDS-PAGE and anti-Rep western blotting (FIG. 1).

(67) B. Characterization of Wildtype or Mutant Rep Protein Under Non-Denaturing Conditions Using Native PAGE

(68) Characterization of the same non-denatured (native) Rep proteins by blue native PAGE also showed significantly less high molecular weight protein aggregates (high molecular weight smear) for the double mutant when compared to the wildtype, both for detection by western blotting (WB, anti-Rep) or by high sensitivity total protein staining (silver staining) (FIG. 2). However, in general, under native PAGE conditions the oligomeric species of Rep (MW of about 150 kDa) represents the dominating Rep protein species. These might be either trimers or tetramers of monomeric Rep (38.2 kDa theoretical MW).

(69) C. Characterization of Wildtype or Mutant Rep Protein Under Denaturing Conditions Using SDS-PA and Western Blotting

(70) For standard ELISA assays, the Rep protein was purified under denaturing conditions from E. coli for high yield production and better protein stability (see protocol below). To characterize aggregation of denatured Rep WT and Rep MUT, the proteins were buffered for 1 h in PBS, to mimic renaturing ELISA coating and blocking conditions, and then subjected to either SDS-PAGE and western blotting with anti-Rep antibodies or Coomassie protein staining (FIG. 3). Again, the Rep mutant showed a significant reduction (>50%) of Rep oligomers and larger aggregates when compared with the wild-type Rep protein.

(71) D. Characterization of Wildtype or Mutant Rep Protein Under denaturing conditions using BN-PAGE and Western Blotting

(72) Characterization of the same samples (each 5 g) on BN-PAGE and subsequent anti-Rep western blotting also showed significantly less Rep oligomers as well as less high molecular weight aggregates (FIG. 4). An additional species of most obviously monomeric Rep protein was detected under native PAGE conditions only for the Rep mutant.

(73) All results show existence of highly stable Rep oligomers (MW 110 kDa), which even resist SDS treatment during SDS-PAGE. Also highly stable Rep aggregates covering even higher molecular weight ranges (120-170 kDa and higher) are detectable by SDS-PAGE and western blotting. Clearly, the intensity of such high molecular weight aggregates is significantly reduced for the 27/154E Rep double mutant. In general, the presence of Rep aggregates is higher for proteins which were purified under non-denaturing conditions. Anyways, also proteins purified and stored under denaturing conditions show very strong aggregation, which is significantly reduced for the Rep double mutant. This is of special interest, as ELISA experimental setups rely and renaturation of the surface-bound protein antigens, because antibody antigen binding necessitates native conditions.

Example 3

(74) A. ELISA Coating Performance of Wildtype or Mutant Rep Protein

(75) Importantly, the newly engineered double Rep mutant shows a comparable ELISA coating performance when compared to the wild-type Rep protein (assay buffers: casein buffer, superblock buffer, 1% BSA in PBS) (FIG. 5).

(76) B. ELISA Performance of Wildtype or Mutant Rep Protein in Human MS Sera

(77) Additionally, the reactivity of Rep-reactive antibodies in human MS sera was increased by about 40% on average when using the 27/154E Rep double mutant as antigen when compared to wild-type Rep in ELISA assays (FIG. 6.)

Example 4

(78) Purification of Wildtype and Mutant Rep Protein Antigen

(79) A nucleotide acid molecule encoding either the full-length wild-type Rep open reading frame (ORF) identified within the MSBI1 genome, or a nucleotide acid molecule Rep double mutant 27/154E are cloned into an expression plasmid (pEXP5-CT, Invitrogen) enabling protein expression in E. coli. Briefly, chemically competent E. coli (SoluB121, Genlantis) were transfected with the expression plasmid followed by clonal selection on LB-agar plates with ampicillin. High level protein expression clones were selected by protein test expressions in a low volume pre-screening. Therefore clonal cultures were expanded to about 10 ml in LB Amp (37 C., shaking device) until an OD600 of 0.4-0.6 was reached followed by induction of protein expression with isopropyl -D-1-thiogalactopyranoside (IPTG, 0.66 mM) over night at 25 C. on a shaking device.

(80) The target protein expression was determined by SDS-PAGE and Western Blotting of the E. coli lysates (prepared in Lmmli SDS-PAGE sample buffer) with anti-His antibodies reactive against the C-terminal 6His tag of the Rep protein. The initial E. coli culture showing the highest expression of Rep protein was then further expanded to 1000 ml LB Amp, brought to an OD600 of 0.5. Protein expression was induced by IPTG (0.66 mM) over night at 25 C. on a shaking device. Cells were then centrifuged at 6000 g at 4 C., washed with PBS and stored at 80 C. in aliquots (10 aliquots corresponding to each 100 ml of the 1000 ml initial IPTG-induced E. coli culture).

(81) The synthesized Rep protein having the amino acid sequence of SEQ ID NO:1 (wildtype) or SEQ ID NO:11 (mutant) within the E. coli expression is denaturated by adding 20 reaction volumes 8 M urea sample buffer pH 8.0 containing 100 mM NaH2PO4, 10 mM Tris HCl, pH 8.0, 5 mM imidazole, 5 mM beta-mercaptoethanol. The Rep protein was subsequently purified under denaturing conditions (55 mM imidazole for washing and 300 mM imidazole for protein elution) based on a C-terminal His6-tag fused to the Rep protein. The quality of purification was determined by Coomassie protein staining and Western Blotting with anti-Rep protein antibodies. The Rep protein purity is densitometrically calculated and greater 95%. The purified protein is either directly used for ELISA-based serum screening or subjected to SDS-Page followed by transfer blotting onto nitrocellulose membranes for serum incubation of 1D-size-resolved Rep protein membrane stripes.

(82) TABLE-US-00002 SEQUENCESUMMARY SEQ ID NO SEQUENCE 1 AminoacidsequenceofRepproteinencodedbyMSBI1.176(wild- type) MSDLIVKDNALMNASYNLALVEQRLILLAIIEARETGKGINANDPLTVHASSYINQFNVERHT AYQALKDACKDLFARQFSYQEKRERGRINITSRWVSQIGYMDDTATVEIIFAPAVVPLITRLE EQFTQYDIEQISGLSSAYAVRMYELLICWRSTGKTPIIELDEFRKRIGVLDTEYTRTDNLKMR VIELALKQINEHTDITASYEQHKKGRVITGFSFKFKHKKQNSDKTPKNSDSSPRIVKHSQIPT NIVKQPENAKMSDLEHRASRVTGEIMRNRLSDRFKQGDESAIDMMKRIQSEIITDAIADQWES KLEEFGVVF 2 AminoacidsequenceofReppeptidefragment EARETGKGINANDPLTVH 3 AminoacidsequenceofReppeptidefragment KQINEHTDITASYEOHKKGRT 4 His-Tag(withtwoneutralstufferaminoacids) GAHHHHHH 5 T7-Tag MASMTGGQQMG 6 FLAG-Tag DYKDDDDK 7 Strep-II-Tag WSHPQFEK 8 AminoacidsequenceofRepproteinencodedbyMSBI2.176(wild- type) MSKLVVKDNALMNASYNLDLVEQRLILLAIIEARESGKGINANDPLTVHAESYINQFGVHRVT AYQALKDACDNLFARQFSYQSKSEKGNIQNHRSRWVSEIIYIDTEATVKIIFAPAIVPLITRL EEQFTKYDIEQISDLSSAYAIRLYELLICWRSTGKTPIIGLGEFRNRVGVLDSEYHRIAHLKE RVIEHSIKQINEHTDITATYEQHKKGRTITGFSFKFKQKKPKQAEIATETPKTATNDPDTTKP LTEPQTAKYSMILCKLGSISDLSNFPDYPAFANWIGNILRNPEKADEQTAKRIFTALKTETDY SKKN 9 MSBI.1specificepitope NRLSDRF 10 NucleotidesequenceofsynthesizedmutantRepproteinencoding MSBIlRep27/154E(mutantDNA) ATGAGCGACCTGATCGTGAAAGACAATGCCCTGATGAACGCCTCCTACAACCTGGCACTGGTC GAACAGAGACTGATTGAGCTGGCTATCATCGAGGCAAGGGAGACCGGCAAGGGCATCAACGCC AATGACCCCCTGACAGTGCACGCCAGCTCCTACATCAACCAGTTTAATGTGGAGCGCCACACC GCCTATCAGGCCCTGAAGGACGCCTGCAAGGATCTGTTTGCCCGGCAGTTCAGCTACCAGGAG AAGCGGGAGAGAGGCAGGATCAACATCACAAGCAGATGGGTGTCCCAGATCGGCTATATGGAC GATACCGCCACAGTGGAGATCATCTTTGCACCAGCAGTGGTGCCTCTGATCACCAGGCTGGAG GAGCAGTTCACACAGTACGACATCGAGCAGATCTCCGGACTGTCTAGCGCCTACGCCGTGCGC ATGTATGAGCTGCTGATCGAGTGGCGGTCTACCGGCAAGACACCTATCATCGAGCTGGATGAG TTCCGCAAGCGGATCGGCGTGCTGGACACCGAGTACACCAGAACAGATAACCTGAAGATGAGA GTGATCGAGCTGGCCCTGAAGCAGATCAATGAGCACACCGATATCACAGCCTCTTATGAGCAG CACAAGAAGGGCCGCGTGATCACCGGCTTCAGCTTTAAGTTCAAGCACAAGAAGCAGAACTCT GACAAGACACCAAAGAATAGCGATTCCTCTCCCCGGATCGTGAAGCACAGCCAGATCCCTACC AACATCGTGAAGCAGCCAGAGAATGCCAAGATGTCCGACCTGGAGCACAGGGCATCTAGGGTG ACAGGCGAGATCATGAGAAATAGGCTGAGCGATCGGTTCAAGCAGGGCGACGAGTCCGCCATC GATATGATGAAGAGAATCCAGTCCGAGATCATCACCGACGCCATCGCCGATCAGTGGGAATCT AAACTGGAAGAGTTTGGAGTCGTGTTTGGAGCACATCACCATCATCATCACTGA 11 AminoacidsequenceofRepproteinencodedbyMSBI1Rep27/154E (mutantprotein) MSDLIVKDNALMNASYNLALVEQRLIELAIIEARETGKGINANDPLTVHASSYINQFNVERHT AYQALKDACKDLFARQFSYQEKRERGRINITSRWVSQIGYMDDTATVEIIFAPAVVPLITRLE EQFTQYDIEQISGLSSAYAVRMYELLIEWRSTGKTPIIELDEFRKRIGVLDTEYTRTDNLKMR VIELALKQINEHTDITASYEQHKKGRVITGFSFKFKHKKQNSDKTPKNSDSSPRIVKHSQIPT NIVKQPENAKMSDLEHRASRVTGEIMRNRLSDRFKQGDESAIDMMKRIQSEIITDAIADQWES KLEEFGVVF 12 AminoacidsequenceofRepproteinencodedbyMSBI2Rep27/154E (mutantprotein) MSKLVVKDNALMNASYNLDLVEQRLIELAIIEARESGKGINANDPLTVHAESYINQFGVHRVT AYQALKDACDNLFARQFSYQSKSEKGNIQNHRSRWVSEIIYIDTEATVKIIFAPAIVPLITRL EEQFTKYDIEQISDLSSAYAIRLYELLIEWRSTGKTPIIGLGEFRNRVGVLDSEYHRIAHLKE RVIEHSIKQINEHTDITATYEQHKKGRTITGFSFKFKQKKPKQAEIATETPKTATNDPDTTKP LTEPQTAKYSMILCKLGSISDLSNFPDYPAFANWIGNILRNPEKADEQIAKRIFTALKTETDY SKKN

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