FXIII Variants with Improved Properties
The present invention concerns variant factor XIII, wherein the rate of activation of said variant by thrombin is faster than for wild type FXIII. Methods for enhancing fibrin clot formation, pharmaceutical compositions and the use for the manufacture of medicaments wherein the variant factor XIII is applied are disclosed.
1 - 7 . (canceled)
8 . A pharmaceutical composition comprising a variant factor XIII comprising at least one modification of the amino acid sequence in the region comprising position 28-41 of the activation peptide such that the rate of activation of said variant by thrombin is faster than for wild type FXIII.
9 . (canceled)
10 . A pharmaceutical composition according to claim 8 , wherein the modification or modifications is selected from the group consisting of T28D, V29F, E30L, L31A, Q32E, V34(G, L), V35(M,K,Q,R,E,H,L,T,N,S,A), P36(L,V), G38(S,A), V39(F,Y,W,R,M), N40(R,K,W,H,Q,A,S) and L41V.
11 . A pharmaceutical composition according to claim 8 , wherein the residues in position 34-40 has been replaced by an amino acid sequence selected from the group of VVPRSFR, VLPRSFR, VTPRSFR, LLPRSFR, LTPRSFR, VVPRSYR, VLPRSYR, VTPRSYR, LLPRSYR, LTPRSYR or LTPRGVN.
12 . A pharmaceutical composition according to claim 8 further comprising a factor VIIa or a variant factor VIIa.
13 . A kit-of-parts comprising a factor XIII variant comprising at least one modification of the amino acid sequence in the region comprising position 28-41 of the activation peptide such that wherein the rate of activation of said variant by thrombin is faster than for wild type FXIII in a first container and a factor VIIa or variant factor VIIa in a second container.
14 - 17 . (canceled)
18 . A factor XIII variant, wherein at least one amino acid in a region comprising position 28-41 of the activation peptide has been modified, the modification or modifications is being selected from the group consisting of T28D, V29F, E30L, L31A, Q32E, V34(G), V35(M,K,Q,R,E,H,T,N,S,A), P36(L,V), G38(S,A), V39(F,Y,W,R,M), N40(R,K,W,H,Q,A,S) and L41V.
19 . A factor XIII variant according to claim 18 , wherein the residues in position 34-40 been replaced by the amino acid sequence VVPRSFR or VLPRSFR or VTPRSFR or LLPRSFR or LTPRSFR or VVPRSYR or VLPRSYR or VTPRSYR or LLPRSYR or LTPRSYR or LTPRGVN.
20 . A pharmaceutical composition according to claim 10 further comprising factor VIIa or a variant factor VIIa.
21 . A pharmaceutical composition according to claim 11 further comprising factor VIIa or a variant factor VIIa.
22 . A method for enhancing fibrin clot formation in a subject comprising administering to the subject an effective amount of a composition according to claim 8 .
23 . The method of claim 22 , wherein the composition is a composition according to claim 10 .
24 . The method of claim 22 , wherein the composition is a composition according to claim 11 .
25 . The method of claim 22 , wherein the method further comprises administering an effective amount of a factor VIIa or a variant factor VIIa to the subject.
26 . The method of claim 23 , wherein the method further comprises administering an effective amount of a factor VIIa or a variant factor VIIa to the subject.
27 . The method of claim 24 , wherein the method further comprises administering an effective amount of a factor VIIa or a variant factor VIIa to the subject.
28 . The method of claim 22 , wherein the subject is a human.
29 . The method of claim 23 , wherein the subject is a human.
30 . The method of claim 24 , wherein the subject is a human.
31 . The method of claim 26 , wherein the factor VIIa is recombinant human factor VIIa and the subject is a human.
32 . The method of claim 27 , wherein the factor VIIa is recombinant human factor VIIa and the subject is a human.
33 . A kit according to claim 13 , wherein the at least one modification in the factor XIII variant is selected from the group consisting of T28D, V29F, E30L, L31A, Q32E, V34(G, L), V35(M,K,Q,R,E,H,L,T,N,S,A), P36(L,V), G38(S,A), V39(F,Y,W,R,M), N40(R,K,W,H,Q,A,S) and L41V.
34 . A kit according to claim 13 , wherein the residues in position 34-40 of the factor XIII variant has been replaced by an amino acid sequence selected from the group consisting of VVPRSFR, VLPRSFR, VTPRSFR, LLPRSFR, LTPRSFR, VVPRSYR, VLPRSYR, VTPRSYR, LLPRSYR, LTPRSYR, and LTPRGVN.