Patent Application
20180291076
The present invention relates to novel insulins or insulins analogues that are extended with sequences of predominantly polar amino acid residues in order to improve the half-life and stability of the drug substance. The invention also provides pharmaceutical compositions comprising such drug substances, and relates to the use of such drug substances for the treatment or prevention of metabolic disorders.
There is a pronounced desire to provide long-acting, stable and active insulins for the treatment of diabetes, and established methods for obtaining prolongation of action includes i.a. precipitated depots, acylation with fatty (di)acid derivatives for imposing albumin binding, and formation of soluble multihexamers. PEGylation (conjugation of proteins with high molecular weight polydisperse polyethyleneglycol) is also an established technology, but PEG, however, is not biodegradable, and PEG can in some cases accumulate in the body when used chronically. Moreover homogeneous polymers are preferred, but most long-chain polymers are only available in polydisperse form.
Biodegradable polymers with properties otherwise similar to PEG are thus of interest for protein drug engineering. The polymers should be polar in order to preserve aqueous solubility, and impose longer duration of therapeutic action in the body, for example by increasing hydrodynamic volume of the engineered proteins. The polymer must be covalently attached to the protein/insulin, which can be obtained as a chemical conjugate or by recombinant expression in a suitable host cell (as a fusion). The main in vivo prolonging effect of extended proteins may be ascribed to a prolonged absorption phase following subcutaneous administration due to large hydrodynamic volume.
Various solutions towards biodegradable polymers of increased half-lives have been suggested. Thus WO 2008 049931 describe certain peptide extended insulins showing a suitable in vivo half-life; DD 257197 describes a method for obtaining an immobilised active insulin product by the addition of poly-amino acids; DD 286509 describes a method for the preparation of an insulin preparation for rectal application, which preparation is activity stabilised and activity prolonging; Arakawa et al, Nature Biotechnology 1998, 16, 934-938, describe a plant-based cholera toxin B subunit-insulin fusion protein that protects against the development of autoimmune diabetes; WO 2008 019368 A2 describes certain albumin-insulin fusion proteins.
However, the insulins and insulins analogues according to this invention have never been described.
While the polar recombinant extensions described in prior art, often suggesting the use of multiple Ser and Thr residues, may work well in bacterial-based production systems, such amino acid residues tends to get glycosylated in yeast-based expression systems, thereby decreasing the overall yield of proteins containing such extensions. Furthermore, as removal of glycosylated by-products during protein purification is difficult and resource consuming, the provision of alternative extensions solutions is desired out of consideration for an optimisation of yeast-based production processes.
Moreover it has been found that the oligomer extended products of the present invention, comprising the polar amino acids Gln and/or His, are less prone to give high viscosity when compared to other products, e.g. sequences holding multiple Glu (E).
Finally the oligomer extended insulins or insulin analogues of this invention render insulin profiles that have shown an in vivo duration and stability that may allow for a once-daily, or even once-weekly, administration.
Therefore, in its first aspect, the invention provides oligomer extended insulins or insulin analogues, which insulins or insulin analogues are extended at the N-terminal end of the B-chain, and/or from the C-terminal end of the A-chain with an extension consisting only of amino acid residues selected from the group of His (H), Gln (Q), Ala (A), Asp (D), Glu (E), Gly (G), Pro (P), Ser (S) and Thr (T); in which extension:
I) one or both of the amino acid residues selected from the group consisting of His (H) and Gln (Q); which number of amino acid residues of Group I is combined with
II) no more than three times this number of the amino acid residues selected from the group consisting of Ala (A), Asp (D), Glu (E), Gly (G), Pro (P), Ser (S), and Thr (T); to render an oligomer extended insulin or insulin analogue, with an extension comprising of from about 100 to about 800 contiguous amino acid residues.
In another aspect the invention provides a pharmaceutical composition comprising the oligomer extended insulin or insulin analogue of the invention, together with one or more adjuvants, excipients, carriers and/or diluents.
In further aspects the invention relates to the use of the oligomer extended insulin or insulin analogue of the invention as a medicament, and to methods of treatment, prevention or alleviation of a metabolic disease or disorder or condition of a living animal body, including a human, which method comprises the step of administering to such a living animal body in need thereof, a therapeutically effective amount of the oligomer extended insulin or insulin analogue of the invention.
Other objects of the invention will be apparent to the person skilled in the art from the following detailed description and examples.
In a 1st embodiment, the invention provides an oligomer extended insulin or insulin analogue, which insulin or insulin analogue is a two-chain insulin molecule comprising an A- and a B-chain, and which insulin or insulin analogue is extended at the N-terminal end of the B-chain, and/or from the C-terminal end of the A-chain, with an extension consisting only of amino acid residues selected from the group of His (H), Gln (Q), Ala (A), Asp (D), Glu (E), Gly (G), Pro (P), Ser (S) and Thr (T); in which extension:
I) one or both of the (two) amino acid residues selected from the group consisting of His (H) and Gln (Q) (i.e. Group I); which number (i.e. one or two) of amino acid residues of Group I is combined with
II) no more than three times this number (i.e. three or six) of the amino acid residues selected from the group consisting of Ala (A), Asp (D), Glu (E), Gly (G), Pro (P), Ser (S), and Thr (T) (i.e. Group II);
to render an oligomer extended insulin or insulin analogue, with an extension comprising of from about 100 to about 800 contiguous amino acid residues.
This implies that the amino acids selected according to the invention may be repeated as needed in order to obtain an extension of the desired length and size.
In another embodiment, the invention provides an oligomer extended insulin or insulin analogue, which insulin or insulin analogue is a two-chain insulin molecule comprising an A- and a B-chain, and which insulin or insulin analogue is extended at the N-terminal end of the B-chain, and/or from the C-terminal end of the A-chain, with an extension consisting only of amino acid residues selected from the group of His (H), Gln (Q), Ala (A), Asp (D), Glu (E), Gly (G), Pro (P), Ser (S) and Thr (T); which extension is composed of:
I) one or both of the (two) amino acid residues selected from the group consisting of His (H) and Gln (Q) (i.e. Group I); which number (i.e. one or two) of amino acid residues of Group I is combined with
II) no more than three times this number (i.e. three or six) of the amino acid residues selected from the group consisting of Ala (A), Asp (D), Glu (E), Gly (G), Pro (P), Ser (S), and Thr (T) (i.e. Group II);
to render a structural motif, wherein the numbers indicate the stoechiometric proportions of the amino acid residues stated above, and which composition may be repeated or extended to render an oligomer extended insulin or insulin analogue with an extension comprising of from about 100 to about 800 contiguous amino acid residues.
Polar residues are preferred mainly out of consideration for solubility and hydrodynamic size of the final product. Moreover Gln and His, that are both polar amino acids, are devoid of the glycosylation problems associated with Ser and Thr, in particular in relation to yeast expression systems. Finally, extensions with sequences involving a certain balance of Gln and/or His have shown to lower viscosity when compared to extensions with other sequences, e.g. sequences holding multiple Glu (E).
Therefore, in a third embodiment, the oligomer extension of the insulin or insulin analogue of the invention holds no more than one Glu (E) in its structural motif, as defined above.
In a fourth embodiment, the oligomer extended insulin or insulin analogue of the invention is a product wherein:
I) one of the (two) amino acid residues selected from the group consisting of His (H) and Gln (Q) (i.e. Group I); is combined with
II) no more than three of the amino acid residues selected from the group consisting of Ala (A), Asp (D), Glu (E), Gly (G), Pro (P), Ser (S) and Thr (T) (i.e. Group II).
In a fifth embodiment, the oligomer extended insulin or insulin analogue of the invention is a product wherein:
I) one of the (two) amino acid residues selected from the group consisting of His (H) and Gln (Q) (i.e. Group I); is combined with
II) no more than three of the amino acid residues selected from the group consisting of Ala (A), Glu (E), Gly (G), and Pro (P), (i.e. Group II).
In a sixth embodiment, the oligomer extended insulin or insulin analogue of the invention is a product wherein:
I) both of the (two) amino acid residues selected from the group consisting of His (H) and Gln (Q) (i.e. Group I); are combined with
II) no more than six of the amino acid residues selected from the group consisting of Ala (A), Asp (D), Glu (E), Gly (G), Pro (P), Ser (S) and Thr (T) (i.e. Group II).
In a seventh embodiment, the oligomer extended insulin or insulin analogue of the invention is a product wherein:
I) both of the (two) amino acid residues selected from the group consisting of His (H) and Gln (Q) (i.e. Group I); are combined with
II) no more than six of the amino acid residues selected from the group consisting of Ala (A), Glu (E), Gly (G), and Pro (P) (i.e. Group II).
In an eight embodiment, one or both of the amino acid residues of Group I are combined with the same number of amino acid residues selected from Group II.
In a ninth embodiment, one or both of the amino acid residues of Group I are combined with 1½ times the number of amino acid residues selected from Group II.
In a tenth embodiment, one or both of the amino acid residues of Group I are combined with 2 times the number of amino acid residues selected from Group II.
In an eleventh embodiment, one or both of the amino acid residues of Group I are combined with 2.5 times the number of amino acid residues selected from Group II.
In a twelfth embodiment, one or both of the amino acid residues of Group I are combined with 3 times the number of amino acid residues selected from Group II.
The extension carried out according to the present invention may be applied to an insulin molecule of any origin, and in particular of recombinant, bovine or porcine origin, or to any insulin analogue at hand.
In a further embodiment of the invention, the oligomer extended product according to the invention is oligomer extended human insulin.
In a 2nd embodiment, the oligomer extended product of the invention is an oligomer extended insulin analogue selected from the group consisting of
A14E, A21G, B16E, B25H, desB30 human insulin;
A14E, A21G, B16H, B25H, desB27, desB30 human insulin;
A14E, A21G, B16H, B25H, desB30 human insulin;
A14E, A21G, B25H, desB30 human insulin;
A14E, A21G, desB30 human insulin;
A14E, A21Q, B16E, B25H, desB30 human insulin;
A14E, A21Q, B16H, B25H, desB27, desB30 human insulin;
A14E, A21Q, B16H, B25H, desB30 human insulin;
A14E, A21G, B25H, desB27, desB30 human insulin;
A14E, A21Q, B25H, desB27, desB30 human insulin;
A14E, A21Q, B25H, desB30 human insulin;
A14E, A21Q, desB30 human insulin;
A14E, B16E, B25H, desB30 human insulin;
A14E, B16H, B25H, desB27, desB30 human insulin;
A14E, B16H, B25H, desB30 human insulin;
A14E, B25H, desB27, desB30 human insulin;
A14E, B25H, desB30 human insulin;
A21G, A22A, A23P, A24Q, desB30 human insulin;
A21G, A22A, A23Q, A24P, desB30 human insulin;
A21G, A22G human insulin;
A21G, A22K, B29R, desB30 human insulin;
A21G, A22P, A23A, A24Q, desB30 human insulin;
A21G, A22P, A23Q, A24A, desB30 human insulin;
A21G, A22Q, A23A, A24P, desB30 human insulin;
A21G, A22Q, A23P, A24A, desB30 human insulin;
A21G, A22Q, A23P, desB30 human insulin;
A21G, B1F, desB30 human insulin;
A21G, B3K, B29E human insulin;
A21G, desB27, desB30 human insulin;
A21G, B28D human insulin;
A21G, B28D, desB30 human insulin;
A21G, B28K, B29P human insulin;
A21G, desB30 human insulin;
A21Q, A22G human insulin;
A21Q, A22K, B29R, desB30 human insulin;
A21Q, B3K, B29E human insulin;
A21Q, desB27, desB30 human insulin;
A21Q, B28D human insulin;
A21Q, B28D, desB30 human insulin;
A21Q, B28K, B29P human insulin;
A21Q, desB30 human insulin;
A22K, B29R, desB30 human insulin;
B3K, B29E human insulin;
B28D human insulin;
B28D, desB30 human insulin;
B28K, B29P human insulin; or
desB30 human insulin.
In one embodiment, the insulin analogue is selected from the group consisting of
A14E, A21G, B25H, desB30 human insulin;
A21G, A22A, A23P, A24Q, desB30 human insulin;
A21G, A22A, A23Q, A24P, desB30 human insulin;
A21G, A22P, A23A, A24Q, desB30 human insulin;
A21G, A22P, A23Q, A24A, desB30 human insulin;
A21G, A22Q, A23A, A24P, desB30 human insulin;
A21G, A22Q, A23P, A24A, desB30 human insulin;
A21G, A22Q, A23P, desB30 human insulin;
A21G, B1F, desB30 human insulin;
A21G, desB30 human insulin; and
A21Q, desB30 human insulin.
In another embodiment, the insulin analogue is selected from the group consisting of
A14E, A21G, B25H, desB30 human insulin;
A21G, desB30 human insulin; and
A21Q, desB30 human insulin.
In a third embodiment, the insulin analogue is A14E, A21G, B25H, desB30 human insulin.
In a fourth embodiment, the insulin analogue is A21G, A22A, A23P, A24Q, desB30 human insulin.
In a fifth embodiment, the insulin analogue is A21G, A22A, A23Q, A24P, desB30 human insulin.
In a sixth embodiment, the insulin analogue is A21G, A22P, A23A, A24Q, desB30 human insulin.
In a seventh embodiment, the insulin analogue is A21G, A22P, A23Q, A24A, desB30 human insulin.
In an eight embodiment, the insulin analogue is A21G, A22Q, A23A, A24P, desB30 human insulin.
In a ninth embodiment, the insulin analogue is A21G, A22Q, A23P, A24A, desB30 human insulin.
In a tenth embodiment, the insulin analogue is A21G, A22Q, A23P, desB30 human insulin.
In an eleventh embodiment, the insulin analogue is A21G, B1F, desB30 human insulin.
In a twelfth embodiment, the insulin analogue is A21G, desB30 human insulin.
In a thirteenth embodiment, the insulin analogue is A21Q, desB30 human insulin.
If the extension begins with a Gly (G) residue, then the insulin analogue selected according to the invention may preferably be an A21Gly (G) containing analogue, or an A21Gln (Q) containing analogue.
Therefore, in one embodiment, the oligomer extended product of the invention is an oligomer extended insulin analogue comprising the A21Gly (G) or A21Gln (Q) mutation, and the extension begins with a Gly (G) residue.
Also, in yet another embodiment, if the insulin analogue holds the native A21N position, then the first amino acid of the N-terminal end of the oligomer extention should not be a Gly (G) residue.
In a 3rd embodiment, the oligomer extended insulin or insulin analogue of the invention is extended at the N-terminal end of the B-chain.
In a 4th embodiment, the oligomer extended insulin or insulin analogue of the invention is extended at the C-terminal end of the A-chain.
In a 5th embodiment, the oligomer extended insulin or insulin analogue of the invention is extended at the N-terminal end of the B-chain and from the C-terminal end of the A-chain.
In a 6th embodiment, the oligomer extended insulin or insulin analogue of the invention is extended with
A) contiguous amino acid residues comprising amino acid residues selected from the group of [A, G, and H or Q]; or from the group of [E, G, and H or Q]; or from the group of [G, P, and H or Q]; (i.e. Group A); or
B) contiguous amino acid residues comprising amino acid residues selected from the group of [A, G, P, and H or Q]; or from the group of [E, G, P, and H or Q]; or from the group of [G, K, P, and H or Q]; or from the group of [E, G, H, and Q]; (i.e. Group B); or
C) contiguous amino acid residues comprising amino acid residues selected from the group of [A, G, P, H, and Q]; or from the group of [E, G, P, H, and Q]; (i.e. Group C); or
D) contiguous amino acid residues comprising amino acid residues selected from the group of [A, E, G, P, H, and Q]; (i.e. Group D];
and/or any combination of Groups A, B, C, and D.
In a 7th embodiment, the oligomer extended insulin or insulin analogue of the invention is extended with non-repeating sequences, i.e. sequences of random order.
In one embodiment, the oligomer extended insulin or insulin analogue of the invention is extended with a sequence of amino acid residues comprising A, D, E, G, H, P, Q, S, and T, in random order.
In another embodiment, the oligomer extended insulin or insulin analogue of the invention is extended with a sequence of amino acid residues comprising A, D, E, G, H, P, and Q, in random order.
In a third embodiment, the oligomer extended insulin or insulin analogue of the invention is extended with a sequence of amino acid residues comprising A, E, G, H, P, Q, S, and T, in random order.
In a fourth embodiment, the oligomer extended insulin or insulin analogue of the invention is extended with a sequence of amino acid residues comprising A, E, G, H, P, and Q, in approximately equal amounts, but in random order.
In an 8th embodiment, the oligomer extended insulin or insulin analogue of the invention is extended with repeats of certain motifs, such motifs may be repeated as needed in order to obtain an extension of the desired length and size. Depending on the motif in question, the number of repeats may be within the range of from about 2 to about 400.
In one embodiment, the number of repeats is within the range of from about 5 to about 250.
In another embodiment, the number of repeats is within the range of from about to about 200.
In a third embodiment, the number of repeats is 10, 12, 13, 15, 20, 25, 30, 31, 33, 37, 40, 44, 49, 50, 56, 60, 62, 65, 66, 67, 69, 70, 75, 80, 90, 100, 125, or 150.
In a 9th embodiment, the amino acid residues of Group A are represented by contiguous amino acid residues selected from the group of [A, G, and H or Q] (i.e. Group A1).
In one embodiment, the amino acid residues of Group A1 are selected from the group of [A, G, and H].
In another embodiment, the amino acid residues of Group A1, selected from the group of [A, G, and H], are represented by one or more of the following motifs: [GHA]; [HAG]; [AGH]; [GAH]; [AHG]; and [HGA]; and any combination hereof.
In a third embodiment, the amino acid residues of Group A1 are selected from the group of [A, G, and Q].
In a fourth embodiment, the amino acid residues of Group A1, selected from the group of [A, G, and Q], are represented by one or more of the following motifs: [GQA]; [QAG]; [AGQ]; [GAQ]; [AQG]; and [QGA]; and any combination hereof.
In a fifth embodiment, the amino acid residues of Group A1, selected from the group of [A, G, and Q], are represented by one or both of the following motifs: [GQA]; and [GAQ]; and any combination hereof.
In a sixth embodiment, the amino acid residues of Group A1, selected from the group of [A, G, and Q], are represented by the motif: [GAQ]; in any combination.
In a 10th embodiment, the amino acid residues of Group A are represented by contiguous amino acid residues selected from the group of [E, G, and H or Q] (i.e. Group A2).
In one embodiment, the amino acid residues of Group A2 are selected from the group of [E, G, and H].
In another embodiment, the amino acid residues of Group A2, selected from the group of [E, G, and H], are represented by one or more of the following motifs: [GEH]; [EHG]; [HGE]; [GHE]; [HEG]; and [EGH]; and any combination hereof.
In a third embodiment, the amino acid residues of Group A2, selected from the group of [E, G, and H], are represented by one or both of the following motifs: [GEH]; and [GHE]; and any combination hereof.
In a fourth embodiment, the amino acid residues of Group A2, selected from the group of [E, G, and H], are represented by the motif: [GEH], in any combination.
In a fifth embodiment, the amino acid residues of Group A2 are selected from the group of [E, G, and Q].
In a sixth embodiment, the amino acid residues of Group A2, selected from the group of [E, G, and Q], are represented by one or more of the following motifs: [GEQ]; [EQG]; [QGE]; [GQE]; [QEG]; and [EGQ]; and any combination hereof.
In a seventh embodiment, the amino acid residues of Group A2, selected from the group of [E, G, and Q], are represented by one or both of the following motifs: [GEQ]; and [GQE]; and any combination hereof.
In an 11th embodiment, the amino acid residues of Group A are represented by contiguous amino acid residues selected from the group of [G, P, and H or Q] (i.e. Group A3).
In one embodiment, the amino acid residues of Group A3 are selected from the group of [G, P, and H].
In another embodiment, the amino acid residues of Group A3, selected from the group of [G, P, and H], are represented by one or more of the following motifs: [GHPH]; [HPHG]; [PHGH]; and [HGHP]; and any combination hereof.
In a third embodiment, the amino acid residues of Group A3, selected from the group of [G, P, and H], are represented by of the motif: [GHPH].
In a fourth embodiment, the amino acid residues of Group A3 are selected from the group of [G, P, and Q].
In a fifth embodiment, the amino acid residues of Group A3, selected from the group of [G, P, and Q], are represented by one or more of the following motifs: [GQP]; [QPG]; and [PGQ]; and any combination hereof.
In a sixth embodiment, the amino acid residues of Group A3, selected from the group of [G, P, and Q], are represented by one or more of the following motifs: [GQPQ]; [QPQG]; [PQGQ]; and [QGQP]; and any combination hereof.
In a seventh embodiment, the amino acid residues of Group A are selected from one or more of the following motifs: [GAQ]; [GEH]; [GEQ]; [GQA]; [GQE]; and/or [GQP]; and any combination hereof.
In a 12th embodiment, the amino acid residues of Group B are represented by contiguous amino acid residues selected from the group of [A, G, P, and H or Q] (i.e. Group B1).
In one embodiment, the amino acid residues of Group B1 are selected from the group of [A,G,P,H].
In another embodiment, the amino acid residues of Group B1, selected from the group of [A,G,P,H], are represented by one or more of the following motifs: [GAPH]; [APHG]; [PHGA]; [HGAP]; [GAHP]; [AHPG]; [HPGA]; [PGAH]; [GPAH]; [PAHG]; [AHGP]; [HGPA]; [GHAP]; [HAPG]; [APGH]; [PGHA]; [GHPA]; [HPAG]; [PAGH]; [AGHP]; [PHAG]; [HAGP]; [AGPH]; and [GPHA]; and any combination hereof.
In a third embodiment, the amino acid residues of Group B1, selected from the group of [A,G,P,H], are represented by the following motif: [GAPH].
In a fourth embodiment, the amino acid residues of Group B1 are selected from the group of [A,G,P,Q].
In a fifth embodiment, the amino acid residues of Group B1, selected from the group of [A,G,P,Q], are represented by one or more of the following motifs: [GAPQ]; [APQG]; [PQGA]; [QGAP]; [GAQP]; [AQPG]; [QPGA]; [PGAQ]; [GPAQ]; [PAQG]; [AQGP]; [QGPA]; [GQAP]; [QAPG]; [APGQ]; [PGQA]; [GQPA]; [QPAG]; [PAGQ]; [AGQP]; [PQAG]; [QAGP]; [AGPQ]; and [GPQA]; and any combination hereof.
In a sixth embodiment, the amino acid residues of Group B1, selected from the group of [A,G,P,Q], are represented by one or more of the following motifs: [GAPQ]; [GAQP]; [GPAQ]; [GQAP]; [GQPA]; [PQAG]; and [GPQA]; and any combination hereof.
In a 13th embodiment, the amino acid residues of Group B are represented by contiguous amino acid residues selected from the group of [E, G, P, and H or Q] (i.e. Group B2).
In one embodiment, the amino acid residues of Group B2 are selected from the group of [E,G,P,H].
In another embodiment, the amino acid residues of Group B2, selected from the group of [E,G,P,H], are represented by one or more of the following motifs: [GEHP]; [EHPG]; [HPGE]; [PGEH]; [GEPH]; [EPHG]; [PHGE]; [HGEP]; [GHPE]; [HPEG]; [PEGH]; [EGHP]; [GHEP]; [HEPG]; [EPGH]; [PGHE]; [GHHP]; [HHPG]; [HPGH]; [PGHH]; [GPEH]; [PEHG]; [EHGP]; [HGPE]; [GPHE]; [PHEG]; [HEGP]; and [EGPH]; and any combination hereof.
In a third embodiment, the amino acid residues of Group B2, selected from the group of [E,G,P,H], are represented by one or more of the following motifs: [GEHP]; [GEPH]; [GHPE]; [GHEP]; [GHHP]; [GPEH]; and [GPHE]; and any combination hereof.
In a fourth embodiment, the amino acid residues of Group B2 are selected from the group of [E,G,P,Q].
In a fifth embodiment, the amino acid residues of Group B2, selected from the group of [E,G,P,Q], are represented by one or more of the following motifs: [GEQP]; [EQPG]; [QPGE]; [PGEQ]; [GEPQ]; [EPQG]; [PQGE]; [QGEP]; [GQPE]; [QPEG]; [PEGQ]; [EGQP]; [GQEP]; [QEPG]; [EPGQ]; [PGQE]; [GQQP]; [QQPG]; [QPGQ]; [PGQQ]; [GPEQ]; [PEQG]; [EQGP]; [QGPE]; [GPQE]; [PQEG]; [QEGP]; and [EGPQ]; and any combination hereof.
In a sixth embodiment, the amino acid residues of Group B2, selected from the group of [E,G,P,Q], are represented by one or more of the following motifs: [GEQP]; [GEPQ]; [GQPE]; [GQEP]; [GPEQ]; and [GPQE]; and any combination hereof.
In a 14th embodiment, the amino acid residues of Group B are represented by contiguous amino acid residues selected from the group of [E, G, H, and Q] (i.e. Group B4).
In one embodiment, the amino acid residues of Group B4 are selected from the group of [E,G,H,Q].
In another embodiment, the amino acid residues of Group B4, selected from the group of [E,G,H,Q], are represented by one or more of the following motifs: [GEQH]; [EQHG]; [QHGE]; [HGEQ]; [GEHQ]; [EHQG]; [HQGE]; [QGEH]; [GHEQ]; [HEQG]; [EQGH]; [QGHE]; [GHQE]; [HQEG]; [QEGH]; [EGHQ]; [GQHP]; [QHPG]; [HPGQ]; [PGQH]; [GQEH]; [QEHG]; [EHGQ]; [HGQE]; [GQHE]; [QHEG]; [HEGQ]; [EGQH]; [GHQP]; [HQPG]; [QPGH]; and [PGHQ]; and any combination hereof.
In a third embodiment, the amino acid residues of Group B4, selected from the group of [E,G,H,Q], are represented by one or more of the following motifs: [GEQH]; [GEHQ]; [GHEQ]; [GHQE]; [GQHP]; [GQEH]; and [GQHE]; and any combination hereof.
In a fourth embodiment, the amino acid residues of Group B are selected from one or more of the following motifs: [GAPH]; [GAPQ]; [GAQP]; [GPAQ]; [GQAP]; [GQPA]; [PQAG]; [GPQA]; [GEHP]; [GEPH]; [GHPE]; [GHEP]; [GHHP]; [GPEH]; [GPHE]; [GEQP]; [GEPQ]; [GQPE]; [GQEP]; [GPEQ]; [GPQE]; [GEQH]; [GEHQ]; [GHEQ]; [GHQE]; [GQHP]; [GQEH]; and/or [GQHE]; and any combination hereof.
In a 15th embodiment, the amino acid residues of Group C are represented by contiguous amino acid residues selected from the group of [A, G, P, H, and Q] (i.e. Group C1).
In one embodiment, the amino acid residues of Group C1, selected from the group of [A, G, P, H, and Q], are represented by one or more of the following motifs: [GHAPGHHP]; [HAPGHHPG]; [APGHHPGH]; [PGHHPGHA]; [GHHPGHAP]; [HHPGHAPG]; [HPGHAPGH]; [PGHAPGHH]; [GHAPGQHP]; [HAPGQHPG]; [APGQHPGH]; [PGQHPGHA]; [GQHPGHAP]; [QHPGHAPG]; [HPGHAPGQ]; [PGHAPGQH]; [GQAPGQHP]; [QAPGQHPG]; [APGQHPGQ]; [PGQHPGQA]; [GQHPGQAP]; [QHPGQAPG]; [HPGQAPGQ]; and [PGQAPGQH]; and any combination hereof.
In another embodiment, the amino acid residues of Group C1, selected from the group of [A, G, P, H, and Q], are represented by one or more of the following motifs:
[GQAPGQAPGAPHGAPH]; [HGQAPGQAPGAPHGAP]; [PHGQAPGQAPGAPHGA]; [APHGQAPGQAPGAPHG]; [GAPHGQAPGQAPGAPH]; [HGAPHGQAPGQAPGAP]; [PHGAPHGQAPGQAPGA]; [APHGAPHGQAPGQAPG]; [GAPHGAPHGQAPGQAP]; [PGAPHGAPHGQAPGQA]; [APGAPHGAPHGQAPGQ]; [QAPGAPHGAPHGQAPG]; [GQAPGAPHGAPHGQAP]; [PGQAPGAPHGAPHGQA]; [APGQAPGAPHGAPHGQ]; [GQAPGAPHGAPHGAPH]; [QAPGAPHGAPHGAPHG]; [APGAPHGAPHGAPHGQ]; [PGAPHGAPHGAPHGQA]; [GAPHGAPHGAPHGQAP]; [APHGAPHGAPHGQAPG]; [PHGAPHGAPHGQAPGA]; [HGAPHGAPHGQAPGAP]; [GAPHGAPHGQAPGAPH]; [APHGAPHGQAPGAPHG]; [PHGAPHGQAPGAPHGA]; [HGAPHGQAPGAPHGAP]; [GAPHGQAPGAPHGAPH]; [APHGQAPGAPHGAPHG]; [PHGQAPGAPHGAPHGA]; [HGQAPGAPHGAPHGAP]; and [QAPGQAPGAPHGAPHG]; and any combination hereof.
In a third embodiment, the amino acid residues of Group C1, selected from the group of [A, G, P, H, and Q], are represented by one or more of the following motifs:
[GQAPGQAPGQAPGAPH]; [HGQAPGQAPGQAPGAP]; [PH GQAPGQAPGQAPGA]; [APHGQAPGQAPGQAPG]; [GAPHGQAPGQAPGQAP]; [PGAPHGQAPGQAPGQA]; [APGAPHGQAPGQAPGQ]; [QAPGAPHGQAPGQAPG]; [GQAPGAPHGQAPGQAP]; [PGQAPGAPHGQAPGQA]; [APGQAPGAPHGQAPGQ]; [QAPGQAPGAPHGQAPG]; [GQAPGQAPGAPHGQAP]; [PGQAPGQAPGAPHGQA]; [APGQAPGQAPGAPHGQ]; and [QAPGQAPGQAPGAPHG]; and any combination hereof.
In a 16th embodiment, the amino acid residues of Group C are represented by contiguous amino acid residues selected from the group of [E, G, P, H, and Q] (i.e. Group C2).
In one embodiment, the amino acid residues of Group C2, selected from the group of [E, G, P, H, and Q], are represented by one or more of the following motifs: [GHEPGHHP]; [HEPGHHPG]; [EPGHHPGH]; [PGHHPGHE]; [GHHPGHEP]; [HHPGHEPG]; [HPGHEPGH]; [PGHEPGHH]; [GHEPGQHP]; [HEPGQHPG]; [EPGQHPGH]; [PGQHPGHE]; [GQHPGHEP]; [QHPGHEPG]; [HPGHEPGQ]; [PGHEPGQH]; [GQEPGQHP]; [QEPGQHPG]; [EPGQHPGQ]; [PGQHPGQE]; [GQHPGQEP]; [QHPGQEPG]; [HPGQEPGQ]; and [PGQEPGQH]; and any combination hereof.
In another embodiment, the amino acid residues of Group C, selected from the group of [E, G, P, H, and Q], are represented by one or more of the following motifs: [GHEPGHHP]; [GHEPGQHP]; and [GQEPGQHP]; and any combination hereof.
In a third embodiment, the amino acid residues of Group C are selected from one or more of the following motifs: [GHEPGHHP]; [GHEPGQHP]; [GQEPGQHP]; [GQAPGAPHGAPHGAPH]; [GQAPGQAPGAPHGAPH]; and/or [GQAPGQAPGQAPGAPH]; and any combination hereof.
In a 17th embodiment, the amino acid residues of Group D are represented by contiguous amino acid residues selected from the group of [A, E, G, P, H, and Q], (i.e. Group D1); or from the group of [A, E, G, H, P, Q] (in random order) (i.e. Group D2).
In one embodiment, the amino acid residues of Group D1, selected from the group of [A, E, G, P, H, and Q], are represented by one or more of the following motifs: [GEHPGAPHGQEPGQAP]; [EH PGAPHGQEPGQAPG]; [HPGAPHGQEPGQAPGE]; [PGAPHGQEPGQAPGEH]; [GAPHGQEPGQAPGEHP]; [APHGQEPGQAPGEHPG]; [PHGQEPGQAPGEHPGA]; [HGQEPGQAPGEHPGAP]; [GQEPGQAPGEHPGAPH]; [QEPGQAPGEHPGAPHG]; [EPGQAPGEHPGAPHGQ]; [PGQAPGEHPGAPHGQE]; [GQAPGEHPGAPHGQEP]; [QAPGEHPGAPHGQEPG]; [APGEHPGAPHGQEPGQ]; [PGEHPGAPHGQEPGQA]; [GQAPGQAPGAPHGAPH]; [QAPGQAPGAPHGAPHG]; [APGQAPGAPHGAPHGQ]; [PGQAPGAPHGAPHGQA]; [GQAPGAPHGAPHGQAP]; [QAPGAPHGAPHGQAPG]; [APGAPHGAPHGQAPGQ]; [PGAPHGAPHGQAPGQA]; [GAPHGAPHGQAPGQAP]; [APHGAPHGQAPGQAPG]; [PHGAPHGQAPGQAPGA]; [HGAPHGQAPGQAPGAP]; [GAPHGQAPGQAPGAPH]; [APHGQAPGQAPGAPHG]; [PHGQAPGQAPGAPHGA]; [HGQAPGQAPGAPHGAP]; [GQAPGQAPGQAPGAPH]; [QAPGQAPGQAPGAPHG]; [APGQAPGQAPGAPHGQ]; [PGQAPGQAPGAPHGQA]; [GQAPGQAPGAPHGQAP]; [QAPGQAPGAPHGQAPG]; [APGQAPGAPHGQAPGQ]; [PGQAPGAPHGQAPGQA]; [GQAPGAPHGQAPGQAP]; [QAPGAPHGQAPGQAPG]; [APGAPHGQAPGQAPGQ]; [PGAPHGQAPGQAPGQA]; [GAPHGQAPGQAPGQAP]; [APHGQAPGQAPGQAPG]; [PH GQAPGQAPGQAPGA]; [HGQAPGQAPGQAPGAP]; [GQEPGAPHGAPHGAPH]; [QEPGAPHGAPHGAPHG]; [EPGAPHGAPHGAPHGQ]; [PGAPHGAPHGAPHGQE]; [GAPHGAPHGAPHGQEP]; [APHGAPHGAPHGQEPG]; [PHGAPHGAPHGQEPGA]; [HGAPHGAPHGQEPGAP]; [GAPHGAPHGQEPGAPH]; [APHGAPHGQEPGAPHG]; [PHGAPHGQEPGAPHGA]; [HGAPHGQEPGAPHGAP]; [GAPHGQEPGAPHGAPH]; [APHGQEPGAPHGAPHG]; [PHGQEPGAPHGAPHGA]; [HGQEPGAPHGAPHGAP]; [GQEPGQEPGAPHGAPH]; [QEPGQEPGAPHGAPHG]; [EPGQEPGAPHGAPHGQ]; [PGQEPGAPHGAPHGQE]; [GQEPGAPHGAPHGQEP]; [QEPGAPHGAPHGQEPG]; [EPGAPHGAPHGQEPGQ]; [PGAPHGAPHGQEPGQE]; [GAPHGAPHGQEPGQEP]; [APHGAPHGQEPGQEPG]; [PHGAPHGQEPGQEPGA]; [HGAPHGQEPGQEPGAP]; [GAPHGQEPGQEPGAPH]; [APHGQEPGQEPGAPHG]; [PHGQEPGQEPGAPHGA]; [HGQEPGQEPGAPHGAP]; [GQEPGQEPGQEPGAPH]; [QEPGQEPGQEPGAPHG]; [EPGQEPGQEPGAPHGQ]; [PGQEPGQEPGAPHGQE]; [GQEPGQEPGAPHGQEP]; [QEPGQEPGAPHGQEPG]; [EPGQEPGAPHGQEPGQ]; [PGQEPGAPHGQEPGQE]; [GQEPGAPHGQEPGQEP]; [QEPGAPHGQEPGQEPG]; [EPGAPHGQEPGQEPGQ]; [PGAPHGQEPGQEPGQE]; [GAPHGQEPGQEPGQEP]; [APHGQEPGQEPGQEPG]; [PHGQEPGQEPGQEPGA]; and [HGQEPGQEPGQEPGAP]; and any combination hereof.
In another embodiment, the amino acid residues of Group D1, selected from the group of [A, E, G, P, H, and Q], are represented by one or more of the following motifs: [GEHPGAPHGQEPGQAP]; [GQAPGAPHGAPHGAPH]; [GQAPGQAPGAPHGAPH]; [GQAPGQAPGQAPGAPH]; [GQEPGAPHGAPHGAPH]; [GQEPGQEPGAPHGAPH]; and [GQEPGQEPGQEPGAPH]; and any combination hereof.
In another embodiment, the amino acid residues of Group D are selected from one or more of the following motifs: [GEHPGAPHGQEPGQAP]; [GQEPGAPHGAPHGAPH]; [GQEPGQEPGAPHGAPH]; and [GQEPGQEPGQEPGAPH]; and any combination hereof.
In an 18th embodiment, the oligomer extended insulin or insulin analogue of the invention is extended with
a motif of Group A selected from [GEH]; [GQA]; [GQE]; [GHE]; [GEQ]; [GAQ]; and [GQP]; and/or any combination hereof; and/or
a motif of Group B selected from [GAPH]; [GAPQ]; [GEHP]; [GEPH]; [GEQH]; [GHEP]; [GHHP]; [PQAG]; [GQAP]; [GQEP]; [GQHP]; [GQPE]; [GEQP]; [GEPQ]; [GPEQ]; [GPQE]; [GQPA]; [GAQP]; [GPAQ]; [GPQA]; [GHPE]; [GPEH]; [GPHE]; [GQEH]; [GQHE]; [GEHQ]; [GHEQ]; and [GHQE]; and/or any combination hereof; and/or
a motif of Group C selected from [GHEP-GHHP]; [GHEP-GQHP]; and [GQEP-GQHP]; and/or any combination hereof; and/or
a motif of Group D selected from [GEHP-GAPH-GQEP-GQAP]; [GQAP-GAPH-GAPH-GAPH]; [GQAP-GQAP-GAPH-GAPH]; [GQAP-GQAP-GQAP-GAPH]; [GQEP-GAPH-GAPH-GAPH]; [GQEP-GQEP-GAPH-GAPH]; and [GQEP-GQEP-GQEP-GAPH]; and/or any combination hereof; and/or
any combination of motifs of Groups A, B, C and D;
which motif may be repeated as needed in order to obtain an extension of the desired length and size.
In a 19th embodiment, the oligomer extended insulin or insulin analogue of the invention is extended with
a motif of Group A selected from [GAQ]; [GEH]; [GEQ]; [GQA]; [GQE]; and [GQP]; and/or any combination hereof; and/or
a motif of Group B selected from [GAPH]; [GAPQ]; [GAQP]; [GEHP]; [GEPH]; [GEPQ]; [GEQH]; [GEQP]; [GHEP]; [GHEQ]; [GHPE]; [GHQE]; [GPAQ]; [GPEH]; [GPEQ]; [GPHE]; [GPQA]; [GPQE]; [GQAP]; [GQEH]; [GQEP]; [GQHE]; [GQPA]; and[GQPE]; and/or any combination hereof; and/or
a motif of Group C selected from [GHEPGQHP]; [GQEPGQHP]; [GQAPGQAPGQAPGAPH]; and [GQAPGQAPGAPHGAPH]; and/or any combination hereof; and/or
a motif of Group D selected from [GEHPGAPHGQEPGQAP]; [GQEPGQEPGQEPGAPH]; [GQEPGQEPGAPHGAPH]; and [A,E,G,P,H,Q]; and/or any combination hereof.
The insulin or insulin analogue may be extended with one or more amino acid residues identified above, and the repeat in question does not have to begin with Gly (G).
The insulin or insulin analogue may be extended with one or more amino acid residues identified above, and the repeat in question can start with any amino acid from the repeat (for example the extended insulin analogue with GAPH repeat can start with APH, PH or H, followed by repeats of GAPH).
In a 20th embodiment, the oligomer extended insulin or insulin analogue of the invention comprises from about 100 to about 800 contiguous amino acid residues in its extension.
In one embodiment, the oligomer extended insulin or insulin analogue of the invention comprises at least about 100 contiguous amino acid residues.
In another embodiment, the oligomer extended insulin or insulin analogue of the invention comprises less than about 800 contiguous amino acid residues.
In a third embodiment, the oligomer extended insulin or insulin analogue of the invention comprises of from about 100 to about 700 contiguous amino acid residues.
In a fourth embodiment, the oligomer extended insulin or insulin analogue of the invention comprises of from about 100 to about 600 contiguous amino acid residues.
In a fifth embodiment, the oligomer extended insulin or insulin analogue of the invention comprises of from about 100 to about 500 contiguous amino acid residues.
In a sixth embodiment, the oligomer extended insulin or insulin analogue of the invention comprises of from about 100 to about 400 contiguous amino acid residues.
In a seventh embodiment, the oligomer extended insulin or insulin analogue of the invention comprises of from about 100 to about 300 contiguous amino acid residues.
In an eight embodiment, the oligomer extended insulin or insulin analogue of the invention comprises of from about 150 to about 300 contiguous amino acid residues.
In a ninth embodiment, the oligomer extended insulin or insulin analogue of the invention comprises of from about 150 to about 250 contiguous amino acid residues.
In a tenth embodiment, the oligomer extended insulin or insulin analogue of the invention comprises of from about 175 to about 225 contiguous amino acid residues.
In an eleventh embodiment, the oligomer extended insulin or insulin analogue of the invention comprises of from about 185 to about 215 contiguous amino acid residues.
In a twelfth embodiment, the oligomer extended insulin or insulin analogue of the invention comprises of from about 190 to about 210 contiguous amino acid residues; and in particular 124, 148, 176, 196, 198, 200, 201, 208, 224, 248, 276, 300, 400, 500, or 600 contiguous amino acid residues.
In a thirteenth embodiment, the oligomer extended insulin or insulin analogue of the invention comprises of from about 190 to about 210 contiguous amino acid residues; and in particular 200, 201, 208 contiguous amino acid residues.
In a 21th embodiment, the oligomer extended insulin or insulin analogue of the invention is a compound of the general Formula I
Ins-Ext (I)
wherein:
“Ins” represents an analogue of human insulin as identified in Table 1 below; and
“Ext” indicates an extension as described in Table 1 below.
In a 22nd embodiment, the oligomer extended insulin or insulin analogue of the invention is a compound selected from
A21Q(GQEP)50, desB30 human insulin;
A21Q(GAPQ)50, desB30 human insulin;
A21Q(GQAP)50, desB30 human insulin;
A21Q(GEPH)50, desB30 human insulin;
A21Q(GEHP)50, desB30 human insulin;
A14E, A21G(GQEP)50, B25H, desB30 human insulin;
A14E, A21G(GAPQ)50, B25H, desB30 human insulin;
A14E, A21G(GEPH)50, B25H, desB30 human insulin;
A14E, A21G(GEHP)50, B25H, desB30 human insulin;
A14E, A21G(GAPH)50, B25H, desB30 human insulin;
A21G(GEHPGAPHGQEPGQAP)13, desB30 human insulin;
A21G(GEH)67, desB30 human insulin;
A21G(GQA)67, desB30 human insulin;
A21G(GQE)67, desB30 human insulin;
A21G(GEQH)50, desB30 human insulin;
A21G(GQEPGQEPGQEPGAPH)12GQEPGQEP, desB30 human insulin;
A21G(GQEPGQEPGAPHGAPH)12GQEPGQEP, desB30 human insulin;
A21G(GQAPGQAPGQAPGAPH)12GQAPGQAP, desB30 human insulin;
A21G(GQAPGQAPGAPHGAPH)12GQAPGQAP, desB30 human insulin;
A21G[A,E,G,H,P,Q] (random 200 amino acids), desB30 human insulin;
A21G(GHEPGQHP)25, desB30 human insulin;
A21G(GQEPGQHP)25, desB30 human insulin;
A21G(GQPE)50, desB30 human insulin;
A21G(GEQP)50, desB30 human insulin;
A21G(GEPQ)50, desB30 human insulin;
A21G(GPEQ)50, desB30 human insulin;
A21G(GPQE)50, desB30 human insulin;
A21G(GQPA)50, desB30 human insulin;
A21G(GAQP)50, desB30 human insulin;
A21G(GPAQ)50, desB30 human insulin;
A21G(GPQA)50, desB30 human insulin;
A21G(GHEP)50, desB30 human insulin;
A21G(GHPE)50, desB30 human insulin;
A21G(GPEH)50, desB30 human insulin;
A21G(GPHE)50, desB30 human insulin;
A21G(GQEH)50, desB30 human insulin;
A21G(GQHE)50, desB30 human insulin;
A21G(GHEQ)50, desB30 human insulin;
A21G(GHQE)50, desB30 human insulin;
A21G(GEQ)67, desB30 human insulin;
A21G(GAQ)67, desB30 human insulin;
A21G(GQAP)62, desB30 human insulin;
A21G(GQAP)75, desB30 human insulin;
A21G(GQAP)100, desB30 human insulin;
A21G(GQAP)50, desB30 human insulin;
A21G(GQAP)125, desB30 human insulin;
A21G(GQAP)150, desB30 human insulin;
A14E, A21G(GQAP)50, B25H, desB30 human insulin;
A14E, A21G(GQAP)75, B25H, desB30 human insulin;
A14E, A21G(GQAP)150, B25H, desB30 human insulin;
A21G, B1F(GQAP)50, desB30 human insulin;
A21G, B1F(GQAP)100, desB30 human insulin;
A21G, A22A, A23P, A24Q(GAPQ)49, desB30 human insulin;
A21G, A22A, A23Q, A24P(GAQP)49, desB30 human insulin;
A21G, A22Q, A23A, A24P(GQAP)49, desB30 human insulin;
A21G, A22Q, A23P, A24A(GQPA)49, desB30 human insulin;
A21G, A22P, A23A, A24Q(GPAQ)49, desB30 human insulin;
A21G, A22P, A23Q, A24A(GPQA)49, desB30 human insulin;
A21G(GQAP)56, desB30 human insulin;
A21G(GQAP)69, desB30 human insulin;
A21G(GQAP)31, desB30 human insulin;
A21G(GQAP)37, desB30 human insulin;
A21G(GQAP)44, desB30 human insulin;
A21G, A22Q, A23P(GQP)66, desB30 human insulin;
A21G, A22A, A23Q, A24P(GAQP)37, desB30 human insulin; and
A21G, A22A, A23Q, A24P(GAQP)62, desB30 human insulin.
Any combination of two or more of the embodiments described herein is considered within the scope of the present invention.
In the context of this invention, the oligomer extended insulin analogues are named relative to human insulin by specification of amino acid deletions, substitutions, insertions and extensions, as also specified by the general Formula I, above.
In this way the compound of e.g. Example 2 represents an analogue of human insulin (A21Q*, desB30), wherein the naturally occurring amino acid residue located in position 21 of the A-chain has been substituted for glutamine (Q), and wherein the naturally occurring amino acid residue located in position B30 has been deleted, and which analogue has been extended in the star-marked position (*) with an extension made up of repeats of the four amino acid residues (GAPQ in the specified order) to make an extension consisting of a total of 200 amino acids residues (which may also be designated as (GAPQ)50)
This analogue may also be designated A21Q(GAPQ)50, desB30 human insulin, and the compound is illustrated in
The oligomer extended insulin or insulin analogue of the invention may be obtained by conventional methods for the preparation of insulin, insulin analogues and insulin derivatives, and in particular the methods described in the working examples.
In brief, insulin-coding DNA is fused with DNA coding for the recombinant extensions. The DNA is transfected into yeast and the extended insulin is expressed and harvested. The extended insulin is expressed as single-chain precursor protein, which precursor protein is subsequently cleaved to obtain a mature, two-chain (A- and B-chain), extended insulin.
In another aspect the invention provides novel oligomer extended insulin or insulin analogue for use as medicaments, or for use in the manufacture of medicaments or pharmaceutical compositions.
In a further aspect, the invention relates to the medical use of the oligomer extended insulin or insulin analogue of the invention, and in particular to the use of such products for the treatment, prevention or alleviation of diseases, disorders or conditions relating to diabetes, Type 1 diabetes, Type 2 diabetes, impaired glucose tolerance, hyperglycemia, dyslipidemia, obesity, metabolic syndrome (metabolic syndrome X, insulin resistance syndrome), hypertension, cognitive disorders, atherosclerosis, myocardial infarction, stroke, cardiovascular disorders, coronary heart disease, inflammatory bowel syndrome, dyspepsia, or gastric ulcers, which method comprises administration to a subject in need thereof a therapeutically effective amount of the insulin derivative of the invention.
In another embodiment, the invention relates to the use of such products for the treatment, prevention or alleviation of diseases, disorders or conditions relating to diabetes, Type 1 diabetes, Type 2 diabetes, or impaired glucose tolerance, which method comprises administration to a subject in need thereof a therapeutically effective amount of the insulin derivative of the invention.
In a third embodiment, the invention relates to the use of such products for the treatment, prevention or alleviation of diseases, disorders or conditions relating to diabetes, and in particular Type 1 diabetes or Type 2 diabetes.
The present invention relates to oligomer extended insulins or insulin analogues useful as medicaments, or for the manufacture of a pharmaceutical composition/medicament, and in particular for use in the treatment, prevention or alleviation of a metabolic disease or disorder or condition.
Therefore, in another aspect, the invention provides novel pharmaceutical compositions comprising a therapeutically effective amount of an oligomer extended insulin or insulin analogue according to the present invention, optionally together with one or more adjuvants, excipients, carriers and/or diluents.
Injectable compositions may be prepared by using conventional techniques, which typically includes dissolving and mixing the ingredients as appropriate to give the desired end product, addition of isotonic agents, preservatives and/or buffers as required, and adjusting the pH value of the solution, e.g. using an acid, for example, hydrochloric acid, or a base, for example, aqueous sodium hydroxide, as needed. Finally, the volume of the solution may be adjusted with water to give the desired concentration of the ingredients.
In one embodiment a solution or suspension is made by dissolving an oligomer extended insulin or insulin analogue of the invention in an aqueous medium at slightly acidic conditions, for example, in a concentration in the range from about 240 to about 2400 μmol/L. The aqueous medium is made isotonic, e.g. using sodium chloride or glycerol. Moreover, the aqueous medium may contain buffers such as acetate or citrate, preservatives such as m-cresol or phenol and zinc ions, e.g. 2 to 5 Zn++ per 6 insulins, or in a concentration of up to about 20 μg of Zn++ per unit of insulin activity. The pH value of the solution may be adjusted towards neutral, without getting too close to the isoelectric point of the compound in question, in order to avoid potential precipitation. The pH value of the final insulin preparation depends upon the concentration of zinc ions, and the concentration of the compound of this invention. The insulin preparation is made sterile, e.g. by sterile filtration.
The present invention relates to drugs for therapeutic use. More specifically the invention relates to the use of the oligomer extended insulin or insulin analogue of the invention for the treatment or prevention of medical conditions relating to diabetes.
Therefore, in another aspect, the invention provides a method for the treatment or alleviation of a disease or disorder or condition of a living animal body, including a human, which disease, disorder or condition may be selected from a disease, disorder or condition relating to diabetes, Type 1 diabetes, Type 2 diabetes, impaired glucose tolerance, hyperglycemia, dyslipidemia, obesity, metabolic syndrome (metabolic syndrome X, insulin resistance syndrome), hypertension, cognitive disorders, atherosclerosis, myocardial infarction, stroke, cardiovascular disorders, coronary heart disease, inflammatory bowel syndrome, dyspepsia, or gastric ulcers, which method comprises the step of administering to a subject in need thereof a therapeutically effective amount of the oligomer extended insulin or insulin analogue of the invention.
In another embodiment the invention provides a method for the treatment or alleviation of a disease or disorder or condition of a living animal body, including a human, which disease, disorder or condition may be selected from a disease, disorder or condition relating to diabetes, Type 1 diabetes, Type 2 diabetes, impaired glucose tolerance, hyperglycemia, dyslipidemia, obesity, metabolic syndrome (metabolic syndrome X, insulin resistance syndrome), hypertension, cognitive disorders, atherosclerosis, myocardial infarction, stroke, cardiovascular disorders, coronary heart disease, inflammatory bowel syndrome, dyspepsia, or gastric ulcers, which method comprises administration to a subject in need thereof a therapeutically effective amount of the oligomer extended insulin or insulin analogue of the invention.
In a third embodiment the invention provides a method for the treatment or alleviation of a disease or disorder or condition of a living animal body, including a human, which disease, disorder or condition may be selected from a disease, disorder or condition relating to diabetes, Type 1 diabetes, Type 2 diabetes, impaired glucose tolerance, hyperglycemia, dyslipidemia, obesity, or metabolic syndrome (metabolic syndrome X, insulin resistance syndrome).
In a fourth embodiment the invention provides a method for the treatment or alleviation of a disease or disorder or condition of a living animal body, including a human, which disease, disorder or condition may be selected from a disease, disorder or condition relating to diabetes, in particular Type 1 diabetes, or Type 2 diabetes.
An exemplary embodiment of the present invention is further illustrated by reference to the accompanying drawing, in which:
The invention is further illustrated with reference to the following examples, which are not intended to be in any way limiting to the scope of the invention as claimed.
The insulin analogue for use according to the invention are produced recombinantly by expressing a DNA sequence encoding the insulin analogue in question in a suitable host cell by well-known techniques, e.g. as disclosed in U.S. Pat. No. 6,500,645. The insulin analogue is either expressed directly or as a precursor molecule, which may have an additional N-terminal extension (in the form of e.g. EEAEAEAPK) on the B-chain and/or a connecting peptide (C-peptide, in the form of e.g. DMK) between the B-chain and the A-chain. This N-terminal extension and C-peptide are cleaved off in vitro by a suitable protease, e.g. Achromobactor lyticus protease (ALP) or trypsin, and therefore will have a cleavage site next to position B1, B29 and A1, respectively. N-terminal extensions and C-peptides of the type suitable for use according to this invention are disclosed in e.g. U.S. Pat. No. 5,395,922, EP 765395, WO 9828429 and WO 2014/195452.
The polynucleotide sequence encoding the insulin analogue precursor for use according to the invention are prepared synthetically by established methods, e.g. the phosphoramidite method described by Beaucage et al. (1981) Tetrahedron Letters 22 1859-1869, or the method described by Matthes et al. (1984) EMBO Journal 3 801-805. According to the phosphoramidite method, oligonucleotides are synthesised in e.g. an automatic DNA synthesiser, purified, duplexed, and ligated to form the synthetic DNA construct. A currently preferred way of preparing the DNA construct is by polymerase chain reaction (PCR).
The recombinant method will typically make use of a vector capable of replicating in the selected microorganism or host cell, and which carries a polynucleotide sequence encoding the insulin analogue precursor for use according to the present invention. The recombinant vector may be an autonomously replicating vector, i.e., a vector which exists as an extra-chromosomal entity, the replication of which is independent of chromosomal replication, e.g. a plasmid, an extra-chromosomal element, a mini-chromosome, or an artificial chromosome. The vector may contain any means for assuring self-replication. Alternatively, the vector may be one which, when introduced into the host cell, is integrated into the genome and replicated together with the chromosome(s) into which it has been integrated. Furthermore, a single vector or plasmid, or two or more vectors or plasmids, which together contain the total DNA to be introduced into the genome of the host cell, or a transposon, may be used. The vector may be a linear or a closed circular plasmid, and will preferably contain an element(s) that permits stable integration of the vector into the host cell's genome or autonomous replication of the vector in the cell independent of the genome.
The recombinant expression vector may be one capable of replicating in yeast. Examples of sequences, which enable the vector to replicate in yeast, are the yeast plasmid 2 μm replication genes REP 1-3 and origin of replication.
The vector may contain one or more selectable markers, which permit easy selection of trans-formed cells. A selectable marker is a gene the product that provides for biocide or viral resistance, resistance to heavy metals, prototrophy to auxotrophs, etc. Examples of bacterial selectable markers are the dal genes from Bacillus subtilis or Bacillus licheniformis, or markers which confer antibiotic resistance, such as ampicillin, kanamycin, chloramphenicol or tetracycline resistance. Selectable markers for use in a filamentous fungal host cell include amdS (acetamidase), argB (orni-thine carbamoyltransferase), pyrG (orotidine-5′-phosphate decarboxylase) and trpC (anthranilate syn-thase). Suitable markers for yeast host cells are ADE2, HIS3, LEU2, LYS2, MET3, TRP1, and URA3. A well suited selectable marker for yeast is the Schizosaccharomyces pompe TPI gene (Russell (1985) Gene 40 125-130).
Within the vector, the polynucleotide sequence is operably connected to a suitable promoter sequence. The promoter may be any nucleic acid sequence that shows transcriptional activity in the host cell of choice, including mutant, truncated, and hybrid promoters, and may be obtained from genes encoding extra-cellular or intra-cellular polypeptides either homologous or heterologous to the host cell.
In a yeast host, examples of useful promoters are the Saccharomyces cerevisiae Ma1, TPI, ADH, TDH3 or PGK promoters.
The polynucleotide sequence encoding the insulin peptide backbone for use according to the invention also will typically be operably connected to a suitable terminator. In yeast, a suitable terminator is the TPI terminator (Alber et al. (1982) J. Mol. Appl. Genet. 1 419-434).
The procedures used to combine the polynucleotide sequence encoding the insulin analogue for use according to the invention, the promoter and the terminator, respectively, and to insert them into a suitable vector containing the information necessary for replication in the selected host, are well known to persons skilled in the art. It will be understood that the vector may be constructed either by first preparing a DNA construct containing the entire DNA sequence encoding the insulin backbones for use according to the invention, and subsequently inserting this fragment into a suitable expression vector, or by sequentially inserting DNA fragments containing genetic information for the individual elements (such as the signal and pro-peptide (N-terminal extension of the B-chain), C-peptide, A- and B-chains), followed by ligation.
The vector comprising the polynucleotide sequence encoding the insulin analogue for use according to the invention is introduced into a host cell, so that the vector is maintained as a chromosomal integrant, or as a self-replicating extra-chromosomal vector. The term “host cell” encompasses any progeny of a parent cell that is not identical to the parent cell due to mutations that occur during replication.
The host cell may in particular be a yeast cell. The yeast organism may be any suitable yeast organism which, on cultivation, secretes the insulin peptide backbone or the precursor hereof into the culture medium. Examples of suitable yeast organisms are include strains selected from Saccharomyces cerevisiae, Saccharomyces kluyveri, Schizosaccharomyces pombe, Sacchoromyces uvarum, Kluyveromyces lactis, Hansenula polymorpha, Pichia pastoris, Pichia methanolica, Pichia kluyveri, Yarrowia lipolytica, Candida sp., Candida utilis, Candida cacaoi, Geotrichum sp., and Geotrichum fermentans.
The transformation of the yeast cells may for instance be effected by protoplast formation followed by transformation by known methods. The medium used to cultivate the cells may be any conventional medium suitable for growing yeast organisms.
The secreted insulin analogue or precursor hereof are recovered from the medium by conventional procedures including separating the yeast cells from the medium by centrifugation, by filtration or by catching or adsorbing the insulin analogue or precursor hereof on an ion exchange matrix or on a reverse phase absorption matrix, precipitating the proteinaceous components of the supernatant, or by filtration by means of a salt, e.g. ammonium sulphate, followed by purification by a variety of chromatographic procedures, e.g. ion exchange chromatography, affinity chromatography, etc.
The purification and digestion of the insulin peptide backbones of this invention is carried out as follows:
The single-chain insulin analogue precursor, which may contain an N-terminal extension of the B-chain, and a modified C-peptide between the B-chain and the A-chain, is purified and concentrated from the yeast culture supernatant by cation exchange (Kjeldsen et al. (1998) Prot. Expr. Pur. 14 309-316).
The single-chain insulin analogue precursor is matured into two-chain insulin peptide backbone by digestion with lysine-specific immobilised Achromobactor lyticus protease (ALP) (Kristensen et al. (1997) J. Biol. Chem. 20 12978-12983) or by use of trypsin to cleave off the N-terminal extension of the B-chain, if present, and the C-peptide.
The eluate from the cation exchange chromatography step containing the insulin analogue precursor is diluted with water to an ethanol concentration of 15-20%. Glycine is added to a concentration of 50 mM and pH is adjusted to 9.0-9.5 by NaOH. Trypsin is added in a proportion of 1:300 (w:w) and digestion is allowed to proceed at 4 degrees. The digestion is analytically monitored every 20 minutes until digestion is completed. The digestion is terminated with addition of 1 M citric acid in a proportion of 3:100 (v:v). The exact amount of trypsin may need to be adjusted for some analogues.
The digestion reaction is analysed by analytical liquid chromatography (LC) on a Waters Acquity Ultra-Performance Liquid Chromatography system using a C18 column and the molecular weight is confirmed by MALDI-TOF mass spectrometry (MS) (Bruker Daltonics Autoflex II TOF/TOF or UltrafleXtreme).
The two-chain insulin analogue is purified by reversed phase HPLC (Waters 600 system) on a C18 column using an acetonitrile gradient. The desired insulin analogue is subsequently recovered by lyophilisation.
Purity of the product may be determined by analytical HPLC, e.g. on a Waters Acquity Ultra-Performance Liquid Chromatography system using a C18 column, and the molecular weight may be confirmed by MALDI-TOF MS or LC-MS (Orbitrap, Thermo Scientific or G2S Synapt, Waters A/S).
The single-chain insulin precursor is matured into two-chain insulin by digestion with lysine-specific immobilized Achromobachter lyticus protease (ALP; Kristensen et al., (1997), J. Biol. Chem. 20, 12978-12983).
The eluate from the cation exchange chromatography step containing the insulin precursor is diluted with water to an ethanol concentration of 15-20%. Sodium glutamate is added to a concentration of 15 mM and pH is adjusted to 9.7 by NaOH. Immobilized ALP is added in a proportion of 1:100 (v:v), and digestion is allowed to proceed with mild stirring in room temperature overnight.
The digestion reaction is analysed by analytical LC on a Waters Acquity Ultra-Performance Liquid Chromatography system using a C4 column and the molecular weight is confirmed by matrix-assisted laser desorption ionization time-of-flight mass spectrometry (Bruker Daltonics Autoflex II TOF/TOF). The immobilized ALP is removed by filtration with a 0.2 μm filter.
The two-chain insulin molecule is purified by reversed phase HPLC (Waters 600 system) on a C18 column using an acetonitrile gradient. The desired insulin or insulin analogue is recovered by lyophilisation.
Purity is determined by analytical LC on a Waters Acquity Ultra-Performance Liquid Chromatography system using a C4 column, and the molecular weight is confirmed by matrix-assisted laser desorption ionization time-of-flight mass spectrometry.
The identity of the analogue precursors were verified in the supernatants by mass spectrometry using analytical HPLC on a Waters Acquity Ultra-Performance Liquid Chromatography system, couplet to a mass spectrometer (Synapt G2, Waters A/S). The average mass was calculated using the MaxEnt1 deconvolution algorithm in MassLynx (Waters A/S).
Parameters used for the HPLC analyses were as follows: Column: Waters ACQUITY UPLC® BEH300 C4 1.7 μm, Column temp: 40° C., Solvent: A: 0.1% FA, B: 0.1% FA in MeCN.
The results of this determination are presented in Table 3 below.
The relative binding affinity of the insulin analogues of the invention for the human insulin receptor (IR) is determined by competition binding in a scintillation proximity assay (SPA) (according to Glendorf T et al. (2008) Biochemistry 47 4743-4751).
In brief, dilution series of a human insulin standard and the insulin analogue to be tested are performed in 96-well Optiplates (Perkin-Elmer Life Sciences) followed by the addition of [125I-A14Y]-human insulin, anti-IR mouse antibody 83-7, solubilised human IR-A (semi-purified by wheat germ agglutinin chromatography from baby hamster kidney (BHK) cells overexpressing the IR-A holoreceptor), and scintillation proximity assay (SPA) beads (Anti-Mouse polyvinyltoluene SPA Beads, GE Healthcare) in binding buffer consisting of 100 mM HEPES (pH 7.8), 100 mM NaCl, 10 mM MgSO4, and 0.025% (v/v) Tween 20. Plates are incubated with gentle shaking for 22-24 h at 22° C., centrifuged at 2000 rpm for 2 minutes and counted on a TopCount NXT (Perkin-Elmer Life Sciences).
Data from the SPA are analysed according to the four-parameter logistic model (Vølund A (1978) Biometrics 34 357-365), and the binding affinities of the analogues calculated relative to that of the human insulin standard measured within the same plate.
The results of this determination are presented in Table 3 below.
This example demonstrates that the compounds representative of the invention indeed target the human insulin receptor.
To investigate the analogues ability to generate a response in vitro selected analogues where tested for their metabolic potency, rFFC, were determined by lipogenesis according to known techniques (Moody A. J. et al. (1974) Metab. Res. 6 12-16 and Rodbell M (1964) J. Biol. Chem. 239 375-365).
Primary rat adipocytes are isolated from the epididymale fat pads and incubated with 3H-glucose in buffer containing 1% fat free HSA and either standard (HI) or ligand. The labelled glucose is converted into extractable lipids in a dose dependent way, resulting in full dose response curves for both ligands. The data were analysed according to a four-parameter logistic model and the affinities were expressed relative to a human insulin standard. The result is expressed as relative potency of ligand compared to standard.
The effect of different amino acid repeats on the large hydrodynamic volume was evaluated by native size exclusion chromatography. The solvent used was: 140 mM NaCl, 10 mM Tris-HCl, 5% (v/v) isopropanol, pH 7.3; and the column: Waters Acquity UPLC BEH450 SEC, 4.6×150 mm, 2.5 uM.
The method was run at 37° C. with a flow of 0.3 ml/min and measured at a wavelength of 280 nm. Selected analogues were analysed in 200 uM solutions. For conversion of the elution retention time to a corresponding mass for a protein, here called SEC size, a standard for size calculation was used: BEH450 SEC protein Standard Mix (P/N18600842).
A non-linear fit (Y=Y0*exp(k*X)) is made in GraphPad prism using the retention time and sizes of the individual proteins in the standard. The constants Y0 and k is found, and the SEC size (Y) is calculated by inserting the retention time (X) of the main peak in the equation.
Human insulin is found as equilibrium between monomer and dimer in this system so this could also be the case for these constructs. The SEC size is more than 5-10 times larger than the expected monomer size. The SEC size is influenced by the amino acid composition and also order of amino acids in the motif.
The pharmacokinetic and pharmacodynamic profiles after single s.c. dosing of 4 nmol/kg insulin analogue to Beagle dogs were investigated.
Eight Beagle dogs were divided in two groups of four animals and dosed in parallel with either the compound of Example 2 or the compound of Example 5.
A single subcutaneous dose of both analogues were well tolerated in Beagle dogs with no clinical signs of hypoglycaemia.
Blood samples were collected and analysed by the LOCI technology. Plasma insulin concentration curves are shown in
The pharmacokinetic profiles after single s.c. dosing of 20 nmol/kg insulin analogue to male Sprague-Dawley rats were investigated.
Non-fasted rats were dosed s.c. in the neck with 20 nmol/kg insulin by the use of needle and syringe with a dose volume of 1 ml/kg. Rats were awake during the experiment with free access to water but not food during the first 8 hour after dosing. Blood samples for insulin analysis were collected regularly for 48 hours after dosing while blood glucose was measured until 8 hours after dosing. Blood samples were analysed by the LOCI technology. Calculated mean residence times (mean±SD) are shown in Table 5 below.
This example demonstrates that the compounds representative of the invention not only target human insulin receptor, but also are capable of effectively lowering the blood glucose, as shown in
The extended insulin analogue appears in MS with a single mass profile. If serine residues are present in the extension sequence, like the GEPS repeat examples, glycosylation is observed (see
The amount of glycosylation for an analogue with GEPS repeats extension lie in the range between 10 and 30%, depending on the number of serine residues, e.g. length of extension sequence (see
Removal of serine residues from the sequence as is seen for the analogues containing G, E, A, H, Q and P result in non-glycosylated extension (see
This example represents a comparative example showing the results of a viscosity determination of oligomer extended insulin analogues representative of the invention (i.e. the compounds of Examples 1-5) compared to the viscosity of an oligomer extended insulin analogues analogue representative of the prior art, i.e. Compound A of the general Formula I, wherein “Ins” represents [A21Q*, desB30]; * indicates point of extension; “Ext” represents the extension “GEPS”; and the number of amino acid residues in the extension is and 200.
The viscosity was estimated by dynamic light scattering (DLS) using a DynaPro PR™ (Wyatt technology, Santa Barbara, Calif., USA). In DLS, the diffusion coefficient is determined, and from that the hydrodynamic radius can be obtained from the Stoke-Einstein equation. Viscosity is included in the Stoke-Einstein equation, and the correct viscosity is needed for an accurate determination of the hydrodynamic radius. By utilizing a molecule of known size (Polystyrene standard Nanosphere beads; diameter mean: 147 nm) and determine the apparent size (changes with viscosity) of this standard in the oligomer extended insulin solutions the actual viscosity can be calculated at a given condition. The apparent bead radius was converted to viscosity (cP): (apparent radius PS bead [nm]/real radius PS bead [nm])×viscosity of solvent (e.g. 0.893 cP at 25° C.).
The results of this determination are presented in Table 6 below, and the figures clearly show the compound representative of the invention have lower viscosity when compared to the compound representative of the prior art.
b10 mM phosphate buffer, pH 7.4, 28 mM m-cresol, 3 Zn2+/6 Ins;
c10 mM phosphate buffer, pH 7.4, 58 mM phenol, 3 Zn2+/6 Ins; and
d20 mM NaCl, pH 7.4, 1.4% glycerol, 19 mM phenol, 19 mM m-cresol, 4 Zn2+/6 Ins.
| Number | Date | Country | Kind |
|---|---|---|---|
| 15170337.8 | Jun 2015 | EP | regional |
| 15176207.7 | Jul 2015 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2016/062514 | 6/2/2016 | WO | 00 |
