Cystine knot peptides binding to alpha IIb beta 3 integrins and methods of use
Disclosed are peptides having a cystine knot structural motif and comprising a sequence engineered for specificity against α IIb β 3 integrin, found on platelets, and a method of using the same in anti-thrombotic therapies. The present peptides utilize a cystine knot scaffold derived from modified agouti-related protein or agatoxin, An alternate library screening strategy was used to isolate variants of peptides that selectively bound to α IIb β 3 integrin or to both α IIb β 3 and α V β 3 integrins. Unique consensus sequences were identified within the identified peptides suggesting alternative molecular recognition events that dictate different integrin binding specificities. In addition, the engineered peptides prevented human platelet aggregation in a plasma-based assay and showed high binding affinity for α IIb β 3 integrin.
1. A knottin peptide binding with high affinity to alpha IIb beta 3 integrin, having a sequence at least 90% identical to the sequence selected from the group consisting of:
(SEQ ID NO: 1)
GCVRLHESCLGQQVPCCDPAATCYCX 1 X 2 RGDX 6 X 7 X 8 X 9 CYCR
and
(SEQ ID NO: 2)
GCIAEDYGRCTWGGTPCCRGRGCICX 1 X 2 RGDX 6 X 7 X 8 X 9 CECT,
where X residues are contained in a loop region and
X 1 is K, L, R, V, Y or N;
X 2 is K or G;
X 6 is W, V, M or R;
X 7 is R, K or N;
X 8 is G, E, S, V, R, M, L, Q, or T; and
X 9 is K, R, M or T.
2. The knottin peptide of claim 1 , having essentially no binding to alpha v beta 3 integrin.
3. The knottin peptide of claim 2 wherein X 6 is W and X 7 and X 9 are each independently R or K.
4. The knottin peptide of claim 1 , binding to both alpha IIb beta 3 integrin and alpha v beta 3 integrin, wherein said loop region comprises sequence:
X 1 GRGDVX 7 VX 9 ,
(SEQ ID NO: 134)
wherein X 7 and X 9 are each independently R or K.
5. The knottin peptide of claim 1 having a sequence at least 95% identical to SEQ ID NO: 1, with the proviso that X 1 X 2 RGDX 6 X 7 X 8 X 9 is selected from the group consisting of VGRGDVRRK (SEQ ID NO: 107); RGRGDVKLR, (SEQ ID NO: 112); LKRGDWKGK, (SEQ ID NO: 100); NKRGDWRSK, (SEQ ID NO: 105); and KKRGDWKER (SEQ ID NO: 106).
6. The knottin peptide of claim 1 , wherein the peptide is SEQ ID NO: 1.
7. The knottin peptide of claim 1 , wherein the peptide is SEQ ID NO: 2.
8. The peptide according to claim 1 , further comprised in a composition comprising a pharmaceutically-acceptable carrier.
9. The peptide according to claim 2 , further comprised in a composition comprising a pharmaceutically-acceptable carrier.
10. A knottin peptide having a scaffold at least 90% sequence identical to the agouti peptide according to SEQ ID NO: 1, GCVRLHESCLGQQVPCCDPAATCYC X 1 X 2 RGDX 6 X 7 X 8 X 9 CYCR, with the proviso that
X 1 is K, L, R, V, Y or N;
X 2 is K or G;
X 6 is W, V, M or R;
X 7 is R, K or N;
X 8 is G, E, S, V, R, M, L, Q, or T; and
X 9 is K, R, M or T.
11. A knottin peptide having a scaffold at least 90% identical to the agatoxin sequence GCIAEDYGRCTWGGTPCCRGRGCICX 1 X 2 RGDX 6 X 7 X 8 X 9 CECT (SEQ ID NO: 2), with the proviso that
X 1 is K, L, R, V, Y or N;
X 2 is K or G;
X 6 is W, V, M or R;
X 7 is R, K or N;
X 8 is G, E, S, V, R, M, L, Q, or T; and
X 9 is K, R, M or T.
12. A method of inhibiting platelet aggregation in a mammal which comprises administering an effective amount of a peptide having a sequence at least 90% identical to the sequence selected from the group consisting of: GCVRLHESCLGQQVPCCDPAATCYCX 1 X 2 RGDX 6 X 7 X 8 X 9 CYCR (SEQ ID NO: 1) and GCIAEDYGRCTWGGTPCCRGRGCICX 1 X 2 RGDX 6 X 7 X 8 X 9 CECT (SEQ ID NO: 2), with the proviso that
X 1 is K, L, R, V, Y or N;
X 2 is K or G;
X 6 is W, V, M or R;
X 7 is R, K or N;
X 8 is G, E, S, V, R, M, L, Q, or T; and
X 9 is K, R, M or T.
13. The method of claim 12 , wherein the peptide is contained in a pharmaceutical composition.
14. The method of claim 12 , wherein the mammal is a human.
15. A method for preparing a peptide specifically binding to an alpha IIb beta 3 integrin, and not binding to a non-alpha IIb beta 3 integrin, comprising the steps of:
(a) preparing a library expressing a collection of peptides with different binding properties;
(b) selecting from said collection peptides that bind to alpha IIb beta 3 integrin to obtain a positive pool; and
(c) selecting and removing from said positive pool peptides that bind to said non-alpha IIB beta-3 integrin.
16. The method of claim 15 wherein said peptides are expressed in recombinant yeast.
17. The method of claim 15 wherein said selecting step (b) is repeated to select peptides with higher binding affinity for alpha IIb beta 3 integrin.
18. A peptide binding specifically to alpha IIb beta 3 integrin, having a sequence at least 95% identical to the sequence GCVRLHESCLGQQVPCCDPAATCYCX 1 K RGDWX 7 X 8 X 9 CYCR (SEQ ID NO: 142), where
X 1 is L, R, K, or N;
X 7 is K or R;
X 8 is G, V, S, or E; and
X 9 is K, R, or M.
19. The peptide according to claim 18 comprising SEQ ID NO: 100.
20. A method of inhibiting platelet aggregation comprising contacting platelets with a peptide according to a sequence at least 95% identical to the sequence GCVRLHESCLGQQVPCCDPAATCYCX 1 KRGDWX 7 X 8 X 9 CYCR (SEQ ID NO: 142), where
X 1 is L, R, K, or N;
X 7 is K or R;
X 8 is G, V, S, or E; and
X 9 is K, R, or M.