Single-chain insulin analogues stabilized by a fourth disulfide bridge

Abstract

A single-chain insulin analogue comprises a B-chain insulin polypeptide connected to an A-chain insulin polypeptide by a C-domain polypeptide. The B-chain insulin polypeptide contains a Cysteine substitution at position B4. The A-chain insulin polypeptide contains a Cysteine substitution at position A10. The C-domain polypeptide is 4 to 11 amino acids long. The analogue mitigates the unfavorable activity of this 4th disulfide bridge in conventional two-chain insulin analogues resulting in a duration of insulin signaling similar to that of wild-type insulin. A method of treating a patient with diabetes mellitus comprises the administration of a physiologically effective amount of the protein or a physiologically acceptable salt thereof to a patient. Use of a single-chain insulin analogue of the present invention in an insulin delivery device (such as a pump or pen) or as part of a high-temperature polymer-melt manufacturing process.

Claims

1. A single-chain insulin analogue comprising a B-chain insulin polypeptide sequence connected to an A-chain insulin polypeptide sequence by a C-domain polypeptide sequence; wherein the B-chain insulin polypeptide sequence contains a Cysteine substitution at position B4 relative to the sequence of wild type insulin; wherein the A-chain insulin polypeptide sequence contains a Cysteine substitution at position A10 relative to the sequence of wild type insulin and wherein the C-domain polypeptide sequence is 4 to 11 amino acids long.

2. The single-chain insulin analogue of claim 1, wherein the C-domain polypeptide sequence comprises an N-terminal acidic element and a C-terminal basic element.

3. The single-chain insulin analogue of claim 1, wherein the analogue comprises any one of SEQ ID NOS: 4-31.

4. The single-chain insulin analogue of claim 3, wherein the C-domain polypeptide begins with Glu-Glu.

5. The single-chain insulin of claim 4, wherein the C-domain polypeptide comprises residues 31-36 of SEQ ID NO: 31.

6. The single-chain insulin of claim 5, wherein the analogue comprises SEQ ID NO: 31.

7. The single-chain insulin of claim 4, wherein the C-domain polypeptide comprises residues 31-38 of SEQ ID NO: 30.

8. The single-chain insulin of claim 7, wherein the analogue comprises SEQ ID NO: 30.

9. The single-chain insulin of claim 3, comprising SEQ ID NO: 8.

10. The single-chain insulin analogue of claim 3, wherein the C-domain polypeptide ends with Arg-Arg.

11. The single-chain insulin analogue of claim 10, wherein the analogue is selected from the group consisting of SEQ ID NOs: 5-9, 13-19, 25-29 and 31.

12. The single-chain insulin analogue of claim 3, wherein the C-domain polypeptide ends with Arg-Arg-Ser-Arg.

13. The single-chain insulin analogue of claim 12, wherein the analogue is selected from the group consisting of SEQ ID NOs: 20-24 and 30.

14. A method of lowering the blood sugar of a patient, in need thereof the method comprising administering a physiologically effective amount of a single-chain insulin analogue or a physiologically acceptable salt thereof to the patient, wherein the single-chain insulin analogue comprises a B-chain insulin polypeptide sequence connected to an A-chain insulin polypeptide sequence by a C-domain polypeptide sequence; wherein the B-chain insulin polypeptide sequence contains a Cysteine substitution at position B4 relative to the sequence of wild type insulin; wherein the A-chain insulin polypeptide sequence contains a Cysteine substitution at position A10 relative to the sequence of wild type insulin and wherein the C-domain polypeptide sequence is 4 to 11 amino acids long.

15. The method of claim 14, wherein the analogue comprises any one of SEQ ID NOS: 4-31.

16. The method of claim 14, wherein the C-domain polypeptide begins with Glu-Glu.

17. The method of claim 16, wherein the C-domain polypeptide comprises residues 31-36 of SEQ ID NO: 31.

18. The method of claim 17, wherein the analogue comprises SEQ ID NO: 31.

Description

BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWINGS

(1) FIG. 1A is a schematic representation of the sequence of human proinsulin (SEQ ID NO: 1) including the A- and B-chains and the connecting region shown with flanking dibasic cleavage sites (filled circles) and C-peptide (open circles).

(2) FIG. 1B is a structural model of proinsulin, consisting of an insulin-like moiety and a disordered connecting peptide (dashed line).

(3) FIG. 1C is a schematic representation of the sequence of human insulin indicating the position of residues A6, A7, A11 and A20 in the A-chain (SEQ ID NO: 2) and B7, B19 and B24 in the B-chain (SEQ ID NO: 3).

(4) FIG. 2 provides the 2D .sup.1H-.sup.15N NMR spectrum of a single-chain insulin analogue SCI-2 of the present invention. The spectrum was acquired at pH 7 (as in a prandial formulation) and 37° C.

(5) FIG. 3A is a graph of mean blood-glucose concentrations over time in Sprague-Dawley rats made diabetic with streptozotocin after IV bolus injection of fresh or heat-stressed SCI not containing a fourth disulfide bridge (SCI-1 without 4SS; SEQ ID NO: 32), or fresh or heat stressed Lantus® (N=4; mean glycemia ca. 400 mg/dl). Heat stressed insulin was given gentle agitation at 95° C. for 30 min. Doses for SCIs (nominally 1 IU/rat IV) were calculated in equivalent nanomoles protein/μl. Symbols: () Lantus, 95° C. for 30 min; () fresh Lantus; (⋄) SCI-1 without 4SS, 95° C. for 30 min; and (.diamond-solid.) fresh SCI-1 without 4SS.

(6) FIG. 3B is a graph of the change in blood-glucose concentrations normalized to initial blood glucose concentration over time in Sprague-Dawley rats made diabetic with streptozotocin after IV bolus injection of fresh or heat-stressed SCI not containing a fourth disulfide bridge (SCI-1 without 4SS; SEQ ID NO: 32), or fresh or heat stressed Lantus® (N=4; mean glycemia ca. 400 mg/dl). Heat stressed insulin was given gentle agitation at 95° C. for 30 min. Doses for SCIs (nominally 1 IU/rat IV) were calculated in equivalent nanomoles protein/μl. Symbols: () Lantus, 95° C. for 30 min; () fresh Lantus; (⋄) SCI-1 without 4SS, 95° C. for 30 min; and (.diamond-solid.) fresh SCI-1 without 4SS.

(7) FIG. 3C is a graph of mean blood-glucose concentrations over time in Sprague-Dawley rats made diabetic with streptozotocin after IV bolus injection of fresh or heat-stressed SCIs on gentle agitation at 95° C. for 30 min (N=4; mean glycemia ca. 400 mg/dl). Symbol code: (filled triangle, .box-tangle-solidup.) fresh SCI-1; (open triangle, ) heated SCI-1; (filled square, ) fresh insulin lispro as positive control and (filled circle, ) Lilly diluent (i.e., buffer only) as negative control. Doses for SCIs (nominally 1 IU/rat IV) were calculated in equivalent nanomoles protein/μl.

(8) FIG. 3D is a graph of the change in blood-glucose concentrations normalized to initial blood glucose concentration over time in Sprague-Dawley rats made diabetic with streptozotocin after IV bolus injection of fresh or heat-stressed SCIs on gentle agitation at 95° C. for 30 min (N=4; mean glycemia ca. 400 mg/dl). Symbol code: (filled triangle, .box-tangle-solidup.) fresh SCI-1; (open triangle, ) heated SCI-1; (filled square, ) fresh insulin lispro as positive control; and (filled circle, ) Lilly diluent (i.e., buffer only) as negative control. Doses for SCIs (nominally 1 IU/rat IV) were calculated in equivalent nanomoles protein/μl.

(9) FIG. 4 provides a molecular model of a “doubly-constrained” single-chain insulin analogue, clamped at left side by an engineered 4.sup.th disulfide bridge (asterisk) and at the right side by a foreshortened C domain.

(10) FIG. 5 is a graph showing blood glucose levels for 57 mer SCIs with (squares; 4SS 81-04; SEQ ID NO: 30) and without (diamonds; 81-04; SEQ ID NO: 31) a fourth disulfide bridge from B4 to A10, over time.

DETAILED DESCRIPTION OF THE INVENTION

(11) The present invention is directed toward a single-chain insulin analogue that provides (i) enhanced stability and resistance to fibrillation due to the presence of a 4.sup.th disulfide bridge (cystine B4-A10) and yet (ii) avoids the abnormal prolongation of signaling associated with this modification in the framework of conventional two-chain insulin analogues. The single-chain insulin analogues of the present invention may have an isoelectric point between 4.0 and 6.0 (and so be suitable for formulation under neutral pH conditions as a rapid-acting insulin analogue formulation) or may have an isoelectric point between 6.5 and 8.0 (and so be suitable for formulation under acidic pH conditions as a basal insulin analogue formulation).

(12) The present invention provides a single-chain insulin analogue that comprises a B-chain insulin polypeptide sequence connected to an A-chain insulin polypeptide sequence by a C-domain polypeptide sequence. The B-chain insulin polypeptide sequence contains a Cysteine substitution at position B4. The A-chain insulin polypeptide sequence contains a Cysteine substitution at position A10. The C-domain polypeptide sequence is 4 to 11 amino acids long. In some examples, the single-chain insulin comprises SEQ ID NO: 8, provided below.

(13) The claimed invention includes a C-domain polypeptide comprising an N-terminal acid element, that is, one or more amino acids with acidic side chains. In some examples, the C-domain polypeptide of the single-chain insulin analogue of the present invention begins with Glu-Glu on the N-terminal end. In other examples, the C-domain polypeptide comprises residues 31-36 of SEQ ID NO: 31. In one particular example, the single-chain insulin analogue comprises SEQ ID NO: 31. In other examples, the C-domain polypeptide comprises residues 31-38 of SEQ ID NO: 30. In another particular example, the single-chain insulin analogue comprises SEQ ID NO: 30.

(14) The claimed invention includes a C-domain polypeptide comprising a C-terminal basic element, that is, one or more amino acids with basic side chains. In some examples of the claimed invention, the C-domain polypeptide ends with Arg-Arg. In still other examples, the C-domain polypeptide ends with Arg-Arg-Ser-Arg. In further examples, the C-domain polypeptide ends with Ser-Arg-Arg-Ser-Arg.

(15) The claimed invention also includes DNA or other nucleic acid sequences that encode the single-chain insulin analogues of SEQ ID NOs: 4-31.

(16) The claimed invention further provides a method of treating a patient with diabetes mellitus which comprises the administration of a physiologically effective amount of the single-chain insulin analogue or a physiologically acceptable salt thereof to a patient. Accordingly, the single-chain insulin analogue of the present invention may be used as a medicament or for the manufacture of a medicament for the lowering of the blood sugar of a patient, such as a patient with diabetes mellitus. The single-chain insulin analogue of the present invention may be used in an insulin delivery device such as an insulin pump or pen, or as part of a high-temperature polymer-melt manufacturing process.

(17) The single-chain insulin analogue may be formulated to contain zinc ions at a molar ratio of between 2 and 10 zinc ions per six single-chain insulin analogue monomers and the pH of the formulation may be between pH 3.0 and pH 4.5. The single-chain insulin analogue may be formulated to contain zinc ions at a molar ratio of between 0 and 3 zinc ions per six single-chain insulin analogue monomers and the pH of the formulation may be between pH 6.5 and pH 8.0. It is envisioned that the single-chain insulin analogue may be formulated at a strength of U-100, U-200, U-300, U-400, U-500 or even as high as U-1000.

(18) The invention will be better understood by reference to the following examples which are included for the purpose of illustration and not limitation. Two molecular embodiments of this strategy were prepared by biosynthetic expression in the yeast Pichia pastoris, designated SCI-1 and SCI-2. These candidates differ in isoelectric point (pI) and hence in their pH-dependent solubilities: SCI-1 resembles insulin glargine in that it exhibits prolonged PK on conventional SQ injection whereas SCI-2 resembles insulin lispro in that it exhibits rapid onset of action on SQ injection.

(19) Details of the SCI sequences are as follows. Each contains Cys at positions B4 and A10 in addition to the canonical Cys residues at positions B7, B19, A6, A7, A11 and A20. The C-domain linker sequences differ to simultaneously enable pI tuning and impair binding to the mitogenic IGF Type 1 receptor (IGF-1R). Each A domain contains a stabilizing non-β-branched substitution of Thr.sup.A8, an “Achilles' heel” in human insulin. SCI-1 (SEQ ID NO: 30; 59 residues; 8-residue C domain of sequence Glu-Glu-Gly-Ser-Arg-Arg-Ser-Arg) thus contains Arg.sup.A8 (whose positive charge contributes to its pI shift) whereas SCI-2 (SEQ ID NO: 31; 57 residues; 6-residue C domain of sequence Glu-Glu-Gly-Pro-Arg-Arg) contains His.sup.A8. While not wishing to condition patentability on theory, these variant side chains may interact with the side-chain carboxylate of Glu.sup.A4 to provide a favorable C-cap of the A1-A8 α-helix. SCI-1 contains the substitutions Pro.sup.B28-Arg.sup.B29 and SCI-2 contains substitutions Asp.sup.B28-Pro.sup.B29 (which impairs dimerization and hence can contribute to rapid absorption after subcutaneous injection)). Lysine (present at B29 in WT insulin and at B28 in lispro) was avoided to prevent cleavage in P. pastoris by a lysine-directed protease. Substitution of hyper-exposed Tyr.sup.A14 by Glu it thought to mitigate an unfavorable “reverse-hydrophobic effect” and possibly removes a potential aromatic site of chemical degradation. Neither SCI-1 nor SCI-2 contain the substitution His.sup.B10.fwdarw.Asp, which has been associated with enhanced mitogenicity in cell culture and carcinogenesis in rat testing. The sequences of SCI-1 and SCI-2 are otherwise derived from human insulin and are reflected in SEQ ID NOs: 30 and 31, respectively. Analogous synthetic genes have been prepared and cloned in Pichia pastoris encoding SCI-1 and derivatives of SCI-2.

(20) The C-domain sequence in SCI-1 (EEGSRRSR, residues 31-38 of SEQ ID NO: 30) wherein the acidic element (positions C1 and C2; bold) was introduced in an attempt to impair binding to IGF-1R, Gly (position C3; italics) was introduced as a flexible joint, and an IGF-II C-domain-derived element (positions C4-C8 in the present analog; underlined) was employed in an attempt to reduce immunogenicity and possibly to enhance receptor binding. The formal isoelectric point (pI) of SCI-1 was predicted to be shifted toward neutrality by the combined effects of the C-domain sequence (three additional Arginine residues partially offset by two additional Glutamic acid residues) and an additional titratable Histidine at position A8; the substitution of Arg for Lys at B29 was expected to have a negligible effect on the isoelectric point. The isoelectric point of SCI-2 (in the range 4.0-5.0) is by contrast predicted to be similar to or lower than that of wild-type insulin and so is amenable to formulation at or near neutral pH in the presence or absence of zinc ions.

(21) In view of the similarity between human and animal insulins, and use in the past of animal insulins in human patients with diabetes mellitus, it is also envisioned that other minor modifications in the sequence of insulin may be introduced, especially those substitutions considered “conservative.” For example, additional substitutions of amino acids may be made within groups of amino acids with similar side chains, without departing from the present invention. These include the neutral hydrophobic amino acids: Alanine (Ala or A), Valine (Val or V), Leucine (Leu or L), Isoleucine (Ile or I), Proline (Pro or P), Tryptophan (Trp or W), Phenylalanine (Phe or F) and Methionine (Met or M). Likewise, the neutral polar amino acids may be substituted for each other within their group of Glycine (Gly or G), Serine (Ser or S), Threonine (Thr or T), Tyrosine (Tyr or Y), Cysteine (Cys or C), Glutamine (Glu or Q), and Asparagine (Asn or N). Basic amino acids are considered to include Lysine (Lys or K), Arginine (Arg or R) and Histidine (His or H). Acidic amino acids are Aspartic acid (Asp or D) and Glutamic acid (Glu or E). Unless noted otherwise or wherever obvious from the context, the amino acids noted herein should be considered to be L-amino acids. Standard amino acids may also be substituted by non-standard amino acids belong to the same chemical class. By way of non-limiting example, the basic side chain Lys may be replaced by basic amino acids of shorter side-chain length (Ornithine, Di-aminobutyric acid, or Di-aminopropionic acid). Lys may also be replaced by the neutral aliphatic isostere Norleucine (Nle), which may in turn be substituted by analogues containing shorter aliphatic side chains (Aminobutyric acid or Aminopropionic acid).

(22) The 2D .sup.1H-.sup.15N NMR “fingerprint” spectrum of SCI-2 uniformly labeled with .sup.15N (and with .sup.13C) is provided evidence for a folded structure (FIG. 2).

(23) To evaluate the biological activity, potency, duration of signaling, and thermal stability of the analogues in an animal model, male Sprague-Dawley rats (mean body mass ˜300 grams) were rendered diabetic by treatment with streptozotocin (STZ). Protein solutions containing KP-insulin (insulin Lispro, the active component of Humalog®), insulin Glargine (Lantus®; Sanofi-Aventis), and/or a single-chain insulin of the present invention. A control was provided by injection of protein-free Lilly diluent (obtained from Eli Lilly and Co.) composed of 16 mg glycerin, 1.6 mg meta-cresol, 0.65 mg phenol, and 3.8 mg sodium phosphate pH 7.4. The activity of SCI-1 was evaluated in relation to that of Humalog® (U-100 strength taken from an unexpired commercial vial). SCI-1 was formulated according to the formulation of insulin Glargine in Lantus® except that the pH was adjusted in near 3.5. One unit of each of these formulations (or the equivalent in nanomoles of protein as units have not formally been defined for the analogues of the present invention) and injected IV, and resulting changes in blood glucose concentration were monitored by serial measurements using a clinical glucometer (Hypoguard Advance Micro-Draw meter). Rats were injected subcutaneously at time t=0 in groups of four (N=4). Blood was obtained from the clipped tip of the tail at time 0 and every 10 minutes up to 360 min. SCI-1 of the present invention was found, under conditions of formulation similar to that of Lantus®, to retain a substantial proportion of the biological activity of wild-type insulin, insulin lispro, or insulin glargine.

(24) To test the stability of single-chain insulin analogues under extreme conditions (95° C. for 30 min; FIGS. 3A and 3B), rat studies were performed following IV bolus injection to avoid potential confounding changes in SQ absorption and to enable measurement of the duration of signaling. Results are plotted in relation to blood-glucose concentration (FIG. 3A) and percent change (FIG. 3B). Whereas Lantus lost all activity after 30 min at 95° C. ( in FIG. 3A) versus fresh Lantus ( in FIG. 3A), the activity of a preliminary version of SCI-1 lacking the 4.sup.th disulfide bridge (i.e., with Gln at position B4 and Ile at position A10 as in wild-type human insulin; SEQ ID NO: 32) was largely (but incompletely) maintained: a small reduction was observed in the activity and duration of the SCI, most noticeably between 120-420 min (heated SCI without 4SS, ⋄, versus fresh SCI without 4SS, .diamond-solid.). At time points 240 and 300 min, the decrement in activity was ca. 25 and 40%, respectively.

(25) Such partial inactivation was entirely prevented by introduction of the engineered 4.sup.th disulfide bridge (cystine B4-A10) to create SCI-1. This “doubly-clamped” insulin analog (stabilized at one side by cysteine B4-A10 and at the other side by the foreshortened C domain; FIG. 4) exhibited complete preservation of activity following 30 min exposure to 95° C. in solution (FIGS. 3C and 3D). We note that note that SCI-1 as a single-chain version of a 4-disulfide insulin analog exhibits normal duration of in vivo signaling on IV bolus injection (i.e., the same as insulin lispro in FIGS. 3C and 3D), in contrast to the markedly prolonged signaling exhibited by a two-chain, 4-disulfide analog as described previously. Thus, the present invention provides the surprising results providing the favorable effects of cystine B4-A10 on protein stability while mitigating the unfavorable effect of this modification, i.e., an abnormal prolongation of duration of insulin action in a diabetic animal.

(26) The biological activity of the 57mer SCI-2 (SEQ ID NO: 31; also noted as 4SS 81-04) was compared to a similar single chain insulin that did not have a fourth cystine bridge (noted as 81-04 herein; SEQ ID NO: 32). Providing a dose of 20 micrograms per 300 gram rat, the biological activities are essentially identical. (See FIG. 5) This demonstrates that the introduction of a fourth disulfide bridge into a single-chain insulin analogue molecule does not alter the underlying biological activity of the SCI. This is surprising in view of the prior art, which indicated that in two-chain analogs a marked prolongation of the pharmacodynamic response is observed when introducing the 4th disulfide bridge.

(27) The receptor binding affinity of analogue 81-04 and analogue 4SS 81-04 was also determined. The affinity of 4SS 81-04 for the A isoform of the insulin receptor was determined to be 120±20 percent relative to human insulin (and may in fact be the same as wild type human insulin given the error present; data not shown). Its affinity for the B isoform of the insulin receptor is reduced by between fivefold and tenfold relative to wild type human insulin. This preference for the A isoform is similar to that of the 81-04 parent analogue. Furthermore, the affinity of 4SS 81-04 for the mitogenic IGF Type I receptor (IGF-1R) is reduced by between fivefold and tenfold relative to wild type human insulin (data not shown). Such impaired binding to IGF-1R is desirable from the perspective of potential carcinogenesis on long-term use.

(28) A method for treating a patient with diabetes mellitus comprises administering a single-chain insulin analogue as described herein. It is another aspect of the present invention that the single-chain insulin analogues may be prepared either in yeast (Pichia pastoris) or subject to total chemical synthesis by native fragment ligation. The synthetic route of preparation is preferred in the case of non-standard modifications, such as D-amino-acid substitutions, halogen substitutions within the aromatic rings of Phe or Tyr, or O-linked modifications of Serine or Threonine by carbohydrates; however, it would be feasible to manufacture a subset of the single-chain analogues containing non-standard modifications by means of extended genetic-code technology or four-base codon technology. It is yet another aspect of the present invention that use of non-standard amino-acid substitutions can augment the resistance of the single-chain insulin analogue to chemical degradation or to physical degradation. We further envision the analogues of the present invention providing a method for the treatment of diabetes mellitus or the metabolic syndrome. The route of delivery of the insulin analogue is by subcutaneous injection through the use of a syringe or pen device.

(29) A single-chain insulin analogue of the present invention may also contain other modifications, such as a halogen atom at positions B24, B25, or B26 as described more fully in U.S. Pat. No. 8,921,313, the disclosure of which is incorporated by reference herein. An insulin analogue of the present invention may also contain a foreshortened B-chain due to deletion of residues B1-B3 as described more fully in U.S. Pat. No. 9,725,493, the disclosure of which is incorporated by reference herein.

(30) A pharmaceutical composition may comprise such insulin analogues and which may optionally include zinc. Zinc ions may be included at varying zinc ion:protein ratios, ranging from 2.2 zinc atoms per insulin analogue hexamer to 10 zinc atoms per insulin analogue hexamer. The pH of the formulation may either be in the range pH 3.0-4.5 (as a basal formulation of a pI-shifted single-chain insulin analogue) or be in the range pH 6.5-8.0 (as a prandial insulin formulation of a single-chain insulin analogue whose pI is similar to that of wild-type insulin). In either such formulation, the concentration of the insulin analogue would typically be between about 0.6-5.0 mM; concentrations up to 5 mM may be used in vial or pen; the more concentrated formulations (U-200 or higher, including in the range U-500 through U-1000) may be of particular benefit in patients with marked insulin resistance. Excipients may include glycerol, glycine, arginine, Tris, other buffers and salts, and anti-microbial preservatives such as phenol and meta-cresol; the latter preservatives are known to enhance the stability of the insulin hexamer. Such a pharmaceutical composition may be used to treat a patient having diabetes mellitus or other medical condition by administering a physiologically effective amount of the composition to the patient.

(31) The amino-acid sequence of human proinsulin is provided, for comparative purposes, as SEQ ID NO: 1.

(32) TABLE-US-00001 (human proinsulin) SEQ ID NO: 1 Phe-Val-Asn-Gln-His-Leu-Cys-Gly-Ser-His-Leu- Val-Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg- Gly-Phe-Phe-Tyr-Thr-Pro-Lys-Thr-Arg-Arg-Glu- Ala-Glu-Asp-Leu-Gln-Val-Gly-Gln-Val-Glu-Leu- Gly-Gly-Gly-Pro-Gly-Ala-Gly-Ser-Leu-Gln-Pro- Leu-Ala-Leu-Glu-Gly-Ser-Leu-Gln-Lys-Arg-Gly- Ile-Val-Glu-Gln-Cys-Cys-Thr-Ser-Ile-Cys-Ser- Leu-Tyr-Gln-Leu-Glu-Asn-Tyr-Cys-Asn

(33) The amino-acid sequence of the A chain of human insulin is provided as SEQ ID NO: 2.

(34) TABLE-US-00002 (human A chain) SEQ ID NO: 2 Gly-Ile-Val-Glu-Gln-Cys-Cys-Thr-Ser-Ile-Cys- Ser-Leu-Tyr-Gln-Leu-Glu-Asn-Tyr-Cys-Asn

(35) The amino-acid sequence of the B chain of human insulin is provided as SEQ ID NO: 3.

(36) TABLE-US-00003 (human B chain) SEQ ID NO: 3 Phe-Val-Asn-Gln-His-Leu-Cys-Gly-Ser-His-Leu- Val-Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg- Gly-Phe-Phe-Tyr-Thr-Pro-Lys-Thr

(37) The amino-acid sequence of single-chain insulin analogues of the present invention are given in SEQ ID NO 4-28, containing a fourth cysteine at positions B4-A10 and corresponding to polypeptides of length 55, 57, 57, 58, 59, 60, 61, and 62, such that the SCI contains at least one other stabilizing modification at one or more of the indicated positions.

(38) TABLE-US-00004 SEQ ID NO: 4 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu- Val-Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg- Gly-Xaa.sub.1-Phe-Tyr-Thr-Pro-Xaa.sub.2-Thr- [foreshortened C domain]-Gly-Ile-Val-Glu- Gln-Cys-Cys-Xaa.sub.3-Ser-Cys-Cys-Ser-Leu-Xaa.sub.4- Gln-Leu-Glu-Asn-Tyr-Cys-Xaa.sub.5

(39) Where Xaa.sub.1 indicates Phe, Leu, cyclohexanylalanine or a modification of Phe by a halogen atom (F, Cl or Br) at the ortho or 2-ring position; Xaa.sub.2 indicts Glu, Ala, Ile, Leu, Val, Norleucine, amino-propionic acid or amino-butyric acid; where Xaa.sub.3 is His, Glu, Lys, Arg, or another non-beta-branched polar or charged amino acid (i.e., Gly, Ser, Tyr, Cys, Gln, Asn, Lys, Arg, His, Asp, or Glu); where Xaa.sub.4 is Tyr (as in wild-type insulin), Glu or another non-beta-branched polar or charged amino acid; and where Xaa.sub.5 is Asn as in wild-type insulin or Gly, Ala, Asp, Glu or Ser. The bracketed term “[foreshortened C domain]” designates a connecting peptide domain of length 4-11 residues that contains an acidic residue at either the first (N-terminal) or second peptide position (i.e., residues 31 or 32 of the single-chain insulin analogue). Optionally, Phe.sup.B1 may be deleted to yield a des-B1 analogue, Phe.sup.B1 and Val.sup.B2 both may be omitted to yield a des-[B1, B2] analogue, or Phe.sup.B1, Val.sup.B2 and Asn.sup.A3 may all deleted to yield a des-[B1-B3] single-chain analogue

(40) TABLE-US-00005 SEQ ID NO: 5 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu- Val-Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg- Gly-Phe-Phe-Tyr-Thr-Pro-Xaa.sub.1-Thr-Glu-Glu-Gly- Pro-Arg-Arg-Gly-Ile-Val-Glu-Gln-Cys-Cys-Xaa.sub.2- Ser-Cys-Cys-Ser-Leu-Xaa.sub.3-Gln-Leu-Glu-Asn-Tyr- Cys-Xaa.sub.4

(41) Where Xaa.sub.1 indicates Glu, Ala, Asp, Ile, Leu, Val, Lys, Arg, Norleucine, amino-propionic acid or amino-butyric acid; where Xaa.sub.2 is His, Glu, Lys, Arg, or another non-beta-branched polar or charged amino acid; where Xaa.sub.3 is Tyr (as in wild-type insulin), Glu or another non-beta-branched polar or charged amino acid; and where Xaa.sub.4 is Gly, Glu, Ala, Asn, Asp or Ser. Optionally, Phe.sup.B1 may be deleted to yield a des-B1 analogue, Phe.sup.B1 and Val.sup.B2 both may be omitted to yield a des-[B1, B2] analogue, or Phe.sup.B1, Val.sup.B2 and Asn.sup.A3 may all deleted to yield a des-[B1-B3] single-chain analogue.

(42) TABLE-US-00006 SEQ ID NO: 6 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu- Val-Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg- Gly-Phe-Phe-Tyr-Thr-Pro-Xaa.sub.1-Thr-Glu-Ala-Gly- Pro-Arg-Arg-Gly-Ile-Val-Glu-Gln-Cys-Cys-Xaa.sub.2- Ser-Cys-Cys-Ser-Leu-Xaa.sub.3-Gln-Leu-Glu-Asn-Tyr- Cys-Xaa.sub.4

(43) Where Xaa.sub.1 indicates Glu, Ala, Asp, Ile, Leu, Val, Lys, Arg, Norleucine, amino-propionic acid or amino-butyric acid; where Xaa.sub.2 is His, Glu, Lys, Arg, or another non-beta-branched polar or charged amino acid; where Xaa.sub.3 is Tyr (as in wild-type insulin), Glu or another non-beta-branched polar or charged amino acid; and where Xaa.sub.4 is Gly, Glu, Ala, Asn, Asp or Ser. Optionally, Phe.sup.B1 may be deleted to yield a des-B1 analogue, Phe.sup.B1 and Val.sup.B2 both may be omitted to yield a des-[B1, B2] analogue, or Phe.sup.B1, Val.sup.B2 and Asn.sup.A3 may all deleted to yield a des-[B1-B3] single-chain analogue.

(44) TABLE-US-00007 SEQ ID NO: 7 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu- Val-Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg- Gly-Phe-Phe-Tyr-Thr-Pro-Xaa.sub.1-Thr-Ala-Glu-Gly- Pro-Arg-Arg-Gly-Ile-Val-Glu-Gln-Cys-Cys-Xaa.sub.2- Ser-Cys-Cys-Ser-Leu-Xaa.sub.3-Gln-Leu-Glu-Asn-Tyr- Cys-Xaa.sub.4

(45) Where Xaa.sub.1 indicates Glu, Ala, Asp, Ile, Leu, Val, Lys, Arg, Norleucine, amino-propionic acid or amino-butyric acid; where Xaa.sub.2 is His, Glu, Lys, Arg, or another non-beta-branched polar or charged amino acid; where Xaa.sub.3 is Tyr (as in wild-type insulin), Glu or another non-beta-branched polar or charged amino acid; and where Xaa.sub.4 is Gly, Glu, Ala, Asn, Asp or Ser. Optionally, Phe.sup.B1 may be deleted to yield a des-B1 analogue, Phe.sup.B1 and Val.sup.B2 both may be omitted to yield a des-[B1, B2] analogue, or Phe.sup.B1, Val.sup.B2 and Asn.sup.A3 may all deleted to yield a des-[B1-B3] single-chain analogue.

(46) TABLE-US-00008 SEQ ID NO: 8 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu- Val-Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg- Gly-Phe-Phe-Tyr-Thr-Pro-Xaa.sub.1-Thr-Glu-Glu-Gly- Xaa.sub.2-Arg-Arg-Gly-Ile-Val-Glu-Gln-Cys-Cys-Xaa.sub.3- Ser-Cys-Cys-Ser-Leu-Xaa.sub.4-Gln-Leu-Glu-Asn-Tyr- Cys-Xaa.sub.5

(47) Where Xaa.sub.1 indicates Glu, Ala, Asp, Ile, Leu, Val, Lys, Arg, Norleucine, amino-propionic acid or amino-butyric acid; where Xaa.sub.2 is Pro, Ala, Ser or Glu; where Xaa.sub.3 is His, Glu, Lys, Arg, or another non-beta-branched polar or charged amino acid; where Xaa.sub.4 is Tyr (as in wild-type insulin), Glu or another non-beta-branched polar or charged amino acid; and where Xaa.sub.5 is Gly, Glu, Ala, Asn, Asp or Ser. Optionally, Phe.sup.B1 may be deleted to yield a des-B1 analogue, Phe.sup.B1 and Val.sup.B2 both may be omitted to yield a des-[B1, B2] analogue, or Phe.sup.B1, Val.sup.B2 and Asn.sup.A3 may all deleted to yield a des-[B1-B3] single-chain analogue.

(48) TABLE-US-00009 SEQ ID NO: 9 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu- Val-Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg- Gly-Phe-Phe-Tyr-Thr-Pro-Xaa.sub.1-Thr-Glu-Ala-Gly- Xaa.sub.2-Arg-Arg-Gly-Ile-Val-Glu-Gln-Cys-Cys-Xaa.sub.3- Ser-Cys-Cys-Ser-Leu-Xaa.sub.4-Gln-Leu-Glu-Asn-Tyr- Cys-Xaa.sub.5

(49) Where Xaa.sub.1 indicates Glu, Ala, Asp, Ile, Leu, Val, Lys, Arg, Norleucine, amino-propionic acid or amino-butyric acid; where Xaa.sub.2 is Pro, Ala, Ser or Glu; where Xaa.sub.3 is His, Glu, Lys, Arg, or another non-beta-branched polar or charged amino acid; where Xaa.sub.4 is Tyr (as in wild-type insulin), Glu or another non-beta-branched polar or charged amino acid; and where Xaa.sub.5 is Gly, Glu, Ala, Asn, Asp or Ser. Optionally, Phe.sup.B1 may be deleted to yield a des-B1 analogue, Phe.sup.B1 and Val.sup.B2 both may be omitted to yield a des-[B1, B2] analogue, or Phe.sup.B1, Val.sup.B2 and Asn.sup.A3 may all deleted to yield a des-[B1-B3] single-chain analogue.

(50) TABLE-US-00010 SEQ ID NO: 10 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu- Val-Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg- Gly-Phe-Phe-Tyr-Thr-Pro-Xaa.sub.1-Thr-Glu-Ala-Gly- Xaa.sub.2-Xaa.sub.3-Arg-Gly-Ile-Val-Glu-Gln-Cys-Cys- Xaa.sub.4-Ser-Cys-Cys-Ser-Leu-Xaa.sub.5-Gln-Leu-Glu- Asn-Tyr-Cys-Xaa.sub.6

(51) Where Xaa.sub.1 indicates Glu, Ala, Asp, Ile, Leu, Val, Lys, Arg, Norleucine, amino-propionic acid or amino-butyric acid; where Xaa.sub.2 is Pro, Ala, Ser or Glu; where Xaa.sub.3 is Ala, Ser, Gly, Glu, Gln, or Lys; where Xaa.sub.4 is His, Glu, Lys, Arg, or another non-beta-branched polar or charged amino acid; where Xaa.sub.5 is Tyr (as in wild-type insulin), Glu or another non-beta-branched polar or charged amino acid; and where Xaa.sub.6 is Gly, Glu, Ala, Asn, Asp or Ser. Optionally, Phe.sup.B1 may be deleted to yield a des-B1 analogue, Phe.sup.B1 and Val.sup.B2 both may be omitted to yield a des-[B1, B2] analogue, or Phe.sup.B1, Val.sup.B2 and Asn.sup.A3 may all deleted to yield a des-[B1-B3] single-chain analogue.

(52) TABLE-US-00011 SEQ ID NO: 11 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu- Val-Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg- Gly-Phe-Phe-Tyr-Thr-Pro-Xaa.sub.1-Thr-Glu-Ala-Gly- Xaa.sub.2-Arg-Xaa.sub.3-Gly-Ile-Val-Glu-Gln-Cys-Cys- Xaa.sub.4-Ser-Cys-Cys-Ser-Leu-Xaa.sub.5-Gln-Leu-Glu- Asn-Tyr-Cys-Xaa.sub.6

(53) Where Xaa.sub.1 indicates Glu, Ala, Asp, Ile, Leu, Val, Lys, Arg, Norleucine, amino-propionic acid or amino-butyric acid; where Xaa.sub.2 is Pro, Ala, Ser or Glu; where Xaa.sub.3 is Ala, Ser, Gly, Glu, Gln, or Lys; where Xaa.sub.4 is His, Glu, Lys, Arg, or another non-beta-branched polar or charged amino acid; where Xaa.sub.5 is Tyr (as in wild-type insulin), Glu or another non-beta-branched polar or charged amino acid; and where Xaa.sub.6 is Gly, Glu, Ala, Asn, Asp or Ser. Optionally, Phe.sup.B1 may be deleted to yield a des-B1 analogue, Phe.sup.B1 and Val.sup.B2 both may be omitted to yield a des-[B1, B2] analogue, or Phe.sup.B1, Val.sup.B2 and Asn.sup.A3 may all deleted to yield a des-[B1-B3] single-chain analogue.

(54) TABLE-US-00012 SEQ ID NO: 12 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu- Val-Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg- Gly-Xaa.sub.1-Phe-Tyr-Thr-Xaa.sub.2-Pro-Thr- [foreshortened C domain]-Gly-Ile-Val-Glu-Gln- Cys-Cys-Xaa.sub.3-Ser-Cys-Cys-Ser-Leu-Xaa.sub.4-Gln- Leu-Glu-Asn-Tyr-Cys-Xaa.sub.5

(55) Where Xaa.sub.1 indicates Phe or a modification of Phe by a halogen atom (F, Cl or Br) at the ortho or 2-ring position; Xaa.sub.2 indicates Gln, Glu, Ala, Asn, Asp, Ile, His, Leu, Val, ornithine, di-amino-propionic acid or di-amino-butyric acid; where Xaa.sub.3 is His, Glu, Lys, Arg, or another non-beta-branched polar or charged amino acid; where Xaa.sub.4 is Tyr (as in wild-type insulin), Glu or another non-beta-branched polar or charged amino acid; and where Xaa.sub.5 is Asn as in wild-type insulin or Gly, Ala, Asp, Glu or Ser. The bracketed term “[foreshortened C domain]” designates a connecting peptide domain of length 4-11 residues that contains an acidic residue at either the first (N-terminal) or second peptide position (i.e., residues 31 or 32 of the single-chain insulin analogue). Optionally, Phe.sup.B1 may be deleted to yield a des-B1 analogue, Phe.sup.B1 and Val.sup.B2 both may be omitted to yield a des-[B1, B2] analogue, or Phe.sup.B1, Val.sup.B2 and Asn.sup.A3 may all deleted to yield a des-[B1-B3] single-chain analogue.

(56) TABLE-US-00013 SEQ ID NO: 13 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu- Val-Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg- Gly-Phe-Phe-Tyr-Thr-Xaa.sub.1-Pro-Thr-Glu-Glu-Gly- Pro-Arg-Arg-Gly-Ile-Val-Glu-Gln-Cys-Cys-Xaa.sub.2- Ser-Cys-Cys-Ser-Leu-Xaa.sub.3-Gln-Leu-Glu-Asn-Tyr- Cys-Xaa.sub.4

(57) Where Xaa.sub.1 (corresponding to B28) is Gln, Glu, Ala, Asn, Asp, Ile, His, Leu, Val, ornithine, di-amino-propionic acid or di-amino-butyric acid; Xaa.sub.2 (corresponding to A8) is His, Glu, Lys, Arg or another non-beta branched polar or charged amino acid where Xaa.sub.3 (corresponding to A14) is Tyr (as in wild-type insulin), Glu or another non-beta-branched polar or charged amino acid; and where Xaa.sub.4 is Gly, Glu, Ala, Asn, Asp or Ser. Optionally, Phe.sup.B1 may be deleted to yield a des-B1 analogue, Phe.sup.B1 and Val.sup.B2 both may be omitted to yield a des-[B1, B2] analogue, or Phe.sup.B1, Val.sup.B2 and Asn.sup.A3 may all deleted to yield a des-[B1-B3] single-chain analogue.

(58) TABLE-US-00014 SEQ ID NO: 14 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu- Val-Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg- Gly-Phe-Phe-Tyr-Thr-Xaa.sub.1-Pro-Thr-Glu-Ala-Gly- Pro-Arg-Arg-Gly-Ile-Val-Glu-Gln-Cys-Cys-Xaa.sub.2- Ser-Cys-Cys-Ser-Leu-Xaa.sub.3-Gln-Leu-Glu-Asn-Tyr- Cys-Xaa.sub.4

(59) Where Xaa.sub.1 (B28) is Gln, Glu, Ala, Asn, Asp, Ile, His, Leu, Val, ornithine, di-amino-propionic acid or di-amino-butyric acid; Xaa.sub.2 (A8) is His, Glu, Lys, Arg or another non-beta branched polar or charged amino acid where Xaa.sub.3 (A14) is Tyr (as in wild-type insulin), Glu or another non-beta-branched polar or charged amino acid; and where Xaa.sub.4 (A21) is Gly, Glu, Ala, Asn, Asp or Ser. Optionally, Phe.sup.B1 may be deleted to yield a des-B1 analogue, Phe.sup.B1 and Val.sup.B2 both may be omitted to yield a des-[B1, B2] analogue, or Phe.sup.B1, Val.sup.B2 and Asn.sup.A3 may all deleted to yield a des-[B1-B3] single-chain analogue.

(60) TABLE-US-00015 SEQ ID NO: 15 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu- Val-Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg- Gly-Phe-Phe-Tyr-Thr-Xaa.sub.1-Pro-Thr-Ala-Glu-Gly- Pro-Arg-Arg-Gly-Ile-Val-Glu-Gln-Cys-Cys-Xaa.sub.2- Ser-Cys-Cys-Ser-Leu-Xaa.sub.3-Gln-Leu-Glu-Asn-Tyr- Cys-Xaa.sub.4

(61) Where Xaa.sub.1 (B28) is Gln, Glu, Ala, Asn, Asp, Ile, His, Leu, Val, ornithine, di-amino-propionic acid or di-amino-butyric acid; Xaa.sub.2 (A8) is His, Glu, Lys, Arg or another non-beta branched polar or charged amino acid where Xaa.sub.3 (A14) is Tyr (as in wild-type insulin), Glu or another non-beta-branched polar or charged amino acid; and where Xaa.sub.4 is Gly, Glu, Ala, Asn, Asp or Ser. Optionally, Phe.sup.B1 may be deleted to yield a des-B1 analogue, Phe.sup.B1 and Val.sup.B2 both may be omitted to yield a des-[B1, B2] analogue, or Phe.sup.B1, Val.sup.B2 and Asn.sup.A3 may all deleted to yield a des-[B1-B3] single-chain analogue.

(62) TABLE-US-00016 SEQ ID NO: 16 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu-Val- Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg-Gly-Phe- Phe-Tyr-Thr-Xaa.sub.1-Pro-Thr-Glu-Glu-Gly-Xaa.sub.2-Arg-Arg- Gly-Ile-Val-Glu-Gln-Cys-Cys-Xaa.sub.3-Ser-Cys-Cys-Ser- Leu-Xaa.sub.4-Gln-Leu-Glu-Asn-Tyr-Cys-Xaa.sub.5

(63) Where Xaa.sub.1 (B28) is Gln, Glu, Ala, Asn, Asp, Ile, His, Leu, Val, ornithine, di-amino-propionic acid or di-amino-butyric acid; where Xaa.sub.2 is Pro or Ser; where Xaa.sub.3 (A8) is His, Glu, Lys, Arg or another non-beta branched polar or charged amino acid; where Xaa.sub.4 is Tyr (as in wild-type insulin), Glu or another non-beta-branched polar or charged amino acid; and where Xaa.sub.5 is Gly, Glu, Ala, Asn, Asp or Ser. Optionally, Phe.sup.B1 may be deleted to yield a des-B1 analogue, Phe.sup.B1 and Val.sup.B2 both may be omitted to yield a des-[B1, B2] analogue, or Phe.sup.B1, Val.sup.B2 and Asn.sup.A3 may all deleted to yield a des-[B1-B3] single-chain analogue.

(64) TABLE-US-00017 SEQ ID NO: 17 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu-Val- Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg-Gly-Phe- Phe-Tyr-Thr-Xaa.sub.1-Pro-Thr-Glu-Ala-Gly-Xaa.sub.2-Arg-Arg- Gly-Ile-Val-Glu-Gln-Cys-Cys-Xaa.sub.3-Ser-Cys-Cys-Ser- Leu-Xaa.sub.4-Gln-Leu-Glu-Asn-Tyr-Cys-Xaa.sub.5

(65) Where Xaa.sub.1 (B28) is Gln, Glu, Ala, Asn, Asp, Ile, His, Leu, Val, ornithine, di-amino-propionic acid or di-amino-butyric acid; where Xaa.sub.2 is Pro or Ser; where Xaa.sub.3(A8) is His, Glu, Lys, Arg or another non-beta branched polar or charged amino acid where Xaa.sub.4 (A14) is Tyr (as in wild-type insulin), Glu or another non-beta-branched polar or charged amino acid; and where Xaa.sub.5 is Gly, Glu, Ala, Asn, Asp or Ser. Optionally, Phe.sup.B1 may be deleted to yield a des-B1 analogue, Phe.sup.B1 and Val.sup.B2 both may be omitted to yield a des-[B1, B2] analogue, or Phe.sup.B1, Val.sup.B2 and Asn.sup.A3 may all deleted to yield a des-[B1-B3] single-chain analogue.

(66) TABLE-US-00018 SEQ ID NO: 18 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu-Val- Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg-Gly-Phe- Phe-Tyr-Thr-Xaa.sub.1-Pro-Thr-Glu-Ala-Gly-Xaa.sub.2-Xaa.sub.3-Arg- Gly-Ile-Val-Glu-Gln-Cys-Cys-Xaa.sub.4-Ser-Cys-Cys-Ser- Leu-Xaa.sub.5-Gln-Leu-Glu-Asn-Tyr-Cys-Xaa.sub.6

(67) Where Xaa.sub.1 is Gln, Glu, Ala, Asn, Asp, Ile, His, Leu, Val, ornithine, di-amino-propionic acid or di-amino-butyric acid; where Xaa.sub.2 is Arg, Pro or Ser; where Xaa.sub.3 is Arg or Ser; where Xaa.sub.4 (A8) is His, Glu, Lys, Arg, or another non-beta-branched polar or charged amino acid; where Xaa.sub.5 (A14) is Tyr (as in wild-type insulin), Glu or another non-beta-branched polar or charged amino acid; and where Xaa.sub.6 (A21) is Gly, Glu, Ala, Asn, Asp or Ser. Optionally, Phe.sup.B1 may be deleted to yield a des-B1 analogue, Phe.sup.B1 and Val.sup.B2 both may be omitted to yield a des-[B1, B2] analogue, or Phe.sup.B1, Val.sup.B2 and Asn.sup.A3 may all deleted to yield a des-[B1-B3] single-chain analogue.

(68) TABLE-US-00019 SEQ ID NO: 19 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu-Val- Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg-Gly-Phe- Phe-Tyr-Thr-Xaa.sub.1-Pro-Thr-Glu-Ala-Gly-Xaa.sub.2-Arg-Xaa.sub.3- Gly-Ile-Val-Glu-Gln-Cys-Cys-Xaa.sub.4-Ser-Cys-Cys-Ser- Leu-Xaa.sub.5-Gln-Leu-Glu-Asn-Tyr-Cys-Xaa.sub.6

(69) Where Xaa.sub.1 (B28) is Gln, Glu, Ala, Asn, Asp, Ile, His, Leu, Val, ornithine, di-amino-propionic acid or di-amino-butyric acid; where Xaa.sub.2 is Arg, Pro or Ser; where Xaa.sub.3 is Arg, Pro or Ser; where Xaa.sub.4 (A8) is His, Glu, Lys, Arg, or another non-beta-branched polar or charged amino acid; where Xaa.sub.5 (A14) is Tyr (as in wild-type insulin), Glu or another non-beta-branched polar or charged amino acid; and where Xaa.sub.6 is Gly, Glu, Ala, Asn, Asp or Ser. Optionally, Phe.sup.B1 may be deleted to yield a des-B1 analogue, Phe.sup.B1 and Val.sup.B2 both may be omitted to yield a des-[B1, B2] analogue, or Phe.sup.B1, Val.sup.B2 and Asn.sup.A3 may all deleted to yield a des-[B1-B3] single-chain analogue.

(70) TABLE-US-00020 SEQ ID NO: 20 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu-Val- Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg-Gly-Xaa.sub.1- Phe-Tyr-Thr-Pro-Xaa.sub.2-Thr-Glu-Glu-Gly-Ser-Arg-Arg- Ser-Arg-Gly-Ile-Val-Glu-Gln-Cys-Cys-Xaa.sub.3-Ser-Cys- Cys-Ser-Leu-Xaa.sub.4-Gln-Leu-Glu-Asn-Tyr-Cys-Xaa.sub.5

(71) Where Xaa.sub.1 indicates Phe, Leu, cyclohexanylalanine or a modification of Phe by a halogen atom (F, Cl or Br) at the ortho or 2-ring position; Xaa.sub.2 indicates Arg or Lys; where Xaa.sub.3 is His, Lys, Arg, or another non-beta-branched polar or basic acid; where Xaa.sub.4 is Tyr (as in wild-type insulin), Glu or another non-beta-branched polar or charged amino acid; and optionally where Xaa.sub.5 is Asn as in wild-type insulin or Gly, Ala, Asp, Glu or Ser. Optionally, Phe.sup.B1 may be deleted to yield a des-B1 analogue, Phe.sup.B1 and Val.sup.B2 both may be omitted to yield a des-[B1, B2] analogue, or Phe.sup.B1, Val.sup.B2 and Asn.sup.A3 may all deleted to yield a des-[B1-B3] single-chain analogue.

(72) TABLE-US-00021 SEQ ID NO: 21 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu-Val- Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg-Gly-Xaa.sub.1- Phe-Tyr-Thr-Pro-Arg-Thr-Glu-Glu-Gly-Ser-Arg-Arg- Ser-Arg-Gly-Ile-Val-Glu-Gln-Cys-Cys-Arg-Ser-Cys- Cys-Ser-Leu-Tyr-Gln-Leu-Glu-Asn-Tyr-Cys-Gly

(73) Where Xaa.sub.1 indicates Phe, Leu, cyclohexanylalanine or a modification of Phe by a halogen atom (F, Cl or Br) at the ortho or 2-ring position; Xaa.sub.2 indicates Arg or Lys; where Xaa.sub.3 is His, Lys, Arg, or another non-beta-branched polar or basic acid; where Xaa.sub.4 is Tyr (as in wild-type insulin), Glu or another non-beta-branched polar or charged amino acid; and optionally where Xaa.sub.5 is Asn as in wild-type insulin or Gly, Ala, Asp, Glu or Ser. Optionally, Phe.sup.B1 may be deleted to yield a des-B1 analogue, Phe.sup.B1 and Val.sup.B2 both may be omitted to yield a des-[B1, B2] analogue, or Phe.sup.B1, Val.sup.B2 and Asn.sup.A3 may all deleted to yield a des-[B1-B3] single-chain analogue.

(74) TABLE-US-00022 SEQ ID NO: 22 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu-Val- Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg-Gly-Xaa.sub.1- Phe-Tyr-Thr-Pro-Arg-Thr-Glu-Ala-Gly-Ser-Arg-Arg- Ser-Arg-Gly-Ile-Val-Glu-Gln-Cys-Cys-Arg-Ser-Cys- Cys-Ser-Leu-Tyr-Gln-Leu-Glu-Asn-Tyr-Cys-Gly

(75) Where Xaa.sub.1 indicates Phe, Leu, cyclohexanylalanine or a modification of Phe by a halogen atom (F, Cl or Br) at the ortho or 2-ring position; Xaa.sub.2 indicates Arg or Lys; where Xaa.sub.3 is His, Lys, Arg, or another non-beta-branched polar or basic acid; where Xaa.sub.4 is Tyr (as in wild-type insulin), Glu or another non-beta-branched polar or charged amino acid; and optionally where Xaa.sub.5 is Asn as in wild-type insulin or Gly, Ala, Asp, Glu or Ser. Optionally, Phe.sup.B1 may be deleted to yield a des-B1 analogue, Phe.sup.B1 and Val.sup.B2 both may be omitted to yield a des-[B1, B2] analogue, or Phe.sup.B1, Val.sup.B2 and Asn.sup.A3 may all deleted to yield a des-[B1-B3] single-chain analogue.

(76) TABLE-US-00023 SEQ ID NO: 23 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu-Val- Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg-Gly-Xaa.sub.1- Phe-Tyr-Thr-Pro-Arg-Thr-Ala-Glu-Gly-Ser-Arg-Arg- Ser-Arg-Gly-Ile-Val-Glu-Gln-Cys-Cys-Arg-Ser-Cys- Cys-Ser-Leu-Tyr-Gln-Leu-Glu-Asn-Tyr-Cys-Gly

(77) Where Xaa.sub.1 indicates Phe, Leu, cyclohexanylalanine or a modification of Phe by a halogen atom (F, Cl or Br) at the ortho or 2-ring position; Xaa.sub.2 indicates Arg or Lys; where Xaa.sub.3 is His, Lys, Arg, or another non-beta-branched polar or basic acid; where Xaa.sub.4 is Tyr (as in wild-type insulin), Glu or another non-beta-branched polar or charged amino acid; and optionally where Xaa.sub.5 is Asn as in wild-type insulin or Gly, Ala, Asp, Glu or Ser. Optionally, Phe.sup.B1 may be deleted to yield a des-B1 analogue, Phe.sup.B1 and Val.sup.B2 both may be omitted to yield a des-[B1, B2] analogue, or Phe.sup.B1, Val.sup.B2 and Asn.sup.A3 may all deleted to yield a des-[B1-B3] single-chain analogue.

(78) TABLE-US-00024 SEQ ID NO: 24 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu-Val- Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg-Gly-Xaa.sub.1- Phe-Tyr-Thr-Pro-Arg-Thr-Glu-Glu-Gly-Pro-Arg-Arg- Ser-Arg-Gly-Ile-Val-Glu-Gln-Cys-Cys-Arg-Ser-Cys- Cys-Ser-Leu-Tyr-Gln-Leu-Glu-Asn-Tyr-Cys-Gly

(79) Where Xaa.sub.1 indicates Phe, Leu, cyclohexanylalanine or a modification of Phe by a halogen atom (F, Cl or Br) at the ortho or 2-ring position; Xaa.sub.2 indicates Arg or Lys; where Xaa.sub.3 is His, Lys, Arg, or another non-beta-branched polar or basic acid; where Xaa.sub.4 is Tyr (as in wild-type insulin), Glu or another non-beta-branched polar or charged amino acid; and optionally where Xaa.sub.5 is Asn as in wild-type insulin or Gly, Ala, Asp, Glu or Ser. Optionally, Phe.sup.B1 may be deleted to yield a des-B1 analogue, Phe.sup.B1 and Val.sup.B2 both may be omitted to yield a des-[B1, B2] analogue, or Phe.sup.B1, Val.sup.B2 and Asn.sup.A3 may all deleted to yield a des-[B1-B3] single-chain analogue.

(80) TABLE-US-00025 SEQ ID NO: 25 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu-Val- Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg-Gly-Phe- Phe-Tyr-Thr-Pro-Xaa.sub.1-Thr-Glu-Glu-Arg-Arg-Gly-Ile- Val-Glu-Gln-Cys-Cys-Xaa.sub.2-Ser-Cys-Cys-Ser-Leu-Xaa.sub.3- Gln-Leu-Glu-Asn-Tyr-Cys-Xaa.sub.4

(81) Where Xaa.sub.1 indicates Glu, Ala, Ile, Leu, Val, Norleucine, amino-propionic acid or amino-butyric acid; where Xaa.sub.2 is His, Glu, Lys, Arg, or another non-beta-branched polar or charged amino acid; where Xaa.sub.3 is Tyr (as in wild-type insulin), Glu or another non-beta-branched polar or charged amino acid; and optionally where Xaa.sub.4 is Gly, Glu, Ala, Asn, Asp or Ser. Optionally, Phe.sup.B1 may be deleted to yield a des-B1 analogue, Phe.sup.B1 and Val.sup.B2 both may be omitted to yield a des-[B1, B2] analogue, or Phe.sup.B1, Val.sup.B2 and Asn.sup.A3 may all deleted to yield a des-[B1-B3] single-chain analogue.

(82) TABLE-US-00026 SEQ ID NO: 26 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu-Val- Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg-Gly-Phe- Phe-Tyr-Thr-Pro-Xaa.sub.1-Thr-Glu-Glu-Gly-Arg-Arg-Gly- Ile-Val-Glu-Gln-Cys-Cys-Xaa.sub.2-Ser-Cys-Cys-Ser-Leu- Xaa.sub.3-Gln-Leu-Glu-Asn-Tyr-Cys-Xaa.sub.4

(83) Where Xaa.sub.1 indicates Glu, Ala, Ile, Leu, Val, Norleucine, amino-propionic acid or amino-butyric acid; where Xaa.sub.2 is His, Glu, Lys, Arg, or another non-beta-branched polar or charged amino acid; where Xaa.sub.3 is Tyr (as in wild-type insulin), Glu or another non-beta-branched polar or charged amino acid; and optionally where Xaa.sub.4 is Gly, Glu, Ala, Asn, Asp or Ser. Optionally, Phe.sup.B1 may be deleted to yield a des-B1 analogue, Phe.sup.B1 and Val.sup.B2 both may be omitted to yield a des-[B1, B2] analogue, or Phe.sup.B1, Val.sup.B2 and Asn.sup.A3 may all deleted to yield a des-[B1-B3] single-chain analogue.

(84) TABLE-US-00027 SEQ ID NO: 27 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu-Val- Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg-Gly-Phe- Phe-Tyr-Thr-Pro-Xaa.sub.1-Thr-Glu-Glu-Ala-Arg-Arg-Gly- Ile-Val-Glu-Gln-Cys-Cys-Xaa.sub.2-Ser-Cys-Cys-Ser-Leu- Xaa.sub.3-Gln-Leu-Glu-Asn-Tyr-Cys-Xaa.sub.4

(85) Where Xaa.sub.1 indicates Glu, Ala, Ile, Leu, Val, Norleucine, amino-propionic acid or amino-butyric acid; where Xaa.sub.2 is His, Glu, Lys, Arg, or another non-beta-branched polar or charged amino acid; where Xaa.sub.3 is Tyr (as in wild-type insulin), Glu or another non-beta-branched polar or charged amino acid; and optionally where Xaa.sub.4 is Gly, Glu, Ala, Asn, Asp or Ser. Optionally, Phe.sup.B1 may be deleted to yield a des-B1 analogue, Phe.sup.B1 and Val.sup.B2 both may be omitted to yield a des-[B1, B2] analogue, or Phe.sup.B1, Val.sup.B2 and Asn.sup.A3 may all deleted to yield a des-[B1-B3] single-chain analogue.

(86) TABLE-US-00028 SEQ ID NO: 28 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu-Val- Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg-Gly-Phe- Phe-Tyr-Thr-Pro-Xaa.sub.1-Thr-Glu-Glu-Ser-Arg-Arg-Gly- Ile-Val-Glu-Gln-Cys-Cys-Xaa.sub.2-Ser-Cys-Cys-Ser-Leu- Xaa.sub.3-Gln-Leu-Glu-Asn-Tyr-Cys-Xaa.sub.4

(87) Where Xaa.sub.1 indicates Glu, Ala, Ile, Leu, Val, Norleucine, amino-propionic acid or amino-butyric acid; where Xaa.sub.2 is His, Glu, Lys, Arg, or another non-beta-branched polar or charged amino acid; where Xaa.sub.3 is Tyr (as in wild-type insulin), Glu or another non-beta-branched polar or charged amino acid; and optionally where Xaa.sub.4 is Gly, Glu, Ala, Asn, Asp or Ser. Optionally, Phe.sup.B1 may be deleted to yield a des-B1 analogue, Phe.sup.B1 and Val.sup.B2 both may be omitted to yield a des-[B1, B2] analogue, or Phe.sup.B1, Val.sup.B2 and Asn.sup.A3 may all deleted to yield a des-[B1-B3] single-chain analogue.

(88) TABLE-US-00029 SEQ ID NO: 29 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu-Val- Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg-Gly-Phe- Phe-Tyr-Thr-Pro-Xaa.sub.1-Thr-Glu-Glu-Pro-Arg-Arg-Gly- Ile-Val-Glu-Gln-Cys-Cys-Xaa.sub.2-Ser-Cys-Cys-Ser-Leu- Xaa.sub.3-Gln-Leu-Glu-Asn-Tyr-Cys-Xaa.sub.4

(89) Where Xaa.sub.1 indicates Glu, Ala, Ile, Leu, Val, Norleucine, amino-propionic acid or amino-butyric acid; where Xaa.sub.2 is His, Glu, Lys, Arg, or another non-beta-branched polar or charged amino acid; where Xaa.sub.3 is Tyr (as in wild-type insulin), Glu or another non-beta-branched polar or charged amino acid; and optionally where Xaa.sub.4 is Gly, Glu, Ala, Asn, Asp or Ser. Optionally, Phe.sup.B1 may be deleted to yield a des-B1 analogue, Phe.sup.B1 and Val.sup.B2 both may be omitted to yield a des-[B1, B2] analogue, or Phe.sup.B1, Val.sup.B2 and Asn.sup.A3 may all deleted to yield a des-[B1-B3] single-chain analogue.

(90) TABLE-US-00030 (SCI-1, 59-mer) SEQ ID NO: 30 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu-Val- Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg-Gly-Phe- Phe-Tyr-Thr-Pro-Arg-Thr-Glu-Glu-Gly-Ser-Arg-Arg- Ser-Arg-Gly-Ile-Val-Glu-Gln-Cys-Cys-Arg-Ser-Cys- Cys-Ser-Leu-Tyr-Gln-Leu-Glu-Asn-Tyr-Cys-Asn (SCI-2; 4SS 81-04; 57-mer) SEQ ID NO: 31 Phe-Val-Asn-Cys-His-Leu-Cys-Gly-Ser-His-Leu-Val- Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg-Gly-Phe- Phe-Tyr-Thr-Asp-Pro-Thr-Glu-Glu-Gly-Pro-Arg-Arg- Gly-Ile-Val-Glu-Gln-Cys-Cys-His-Ser-Cys-Cys-Ser- Leu-Glu-Gln-Leu-Glu-Asn-Tyr-Cys-Asn (81-04; 57-mer) SEQ ID NO: 32 Phe-Val-Asn-Gln-His-Leu-Cys-Gly-Ser-His-Leu-Val- Glu-Ala-Leu-Tyr-Leu-Val-Cys-Gly-Glu-Arg-Gly-Phe- Phe-Tyr-Thr-Asp-Pro-Thr-Glu-Glu-Gly-Pro-Arg-Arg- Gly-Ile-Val-Glu-Gln-Cys-Cys-His-Ser-Ile-Cys-Ser- Leu-Glu-Gln-Leu-Glu-Asn-Tyr-Cys-Asn

(91) Based upon the foregoing disclosure, it should now be apparent that the enhanced stability conferred by an engineered 4.sup.th disulfide bridge can be made compatible with unperturbed duration of insulin signaling through the co-engineering of a foreshortened C domain. The resulting single-chain insulin analogues provided will carry out the objects set forth hereinabove. Namely, these modified proteins exhibit enhanced resistance to fibrillation while retaining desirable pharmacokinetic features (conferring rapid or prolonged rates of absorption from a subcutaneous depot as may be therapeutically desired) and maintaining at least a fraction of the biological activity of wild-type insulin. It is, therefore, to be understood that any variations evident fall within the scope of the claimed invention and thus, the selection of specific component elements can be determined without departing from the spirit of the invention herein disclosed and described.