Antidotes to factor XA inhibitors
The present disclosure relates to antidotes to anticoagulants targeting factor Xa. The antidotes are factor Xa protein derivatives that bind to the factor Xa inhibitors thereby substantially neutralizing them but do not assemble into the prothrombinase complex. In one embodiment, the derivatives described herein lack or have reduced intrinsic coagulant activity.
1. An isolated two-chain polypeptide comprising the amino acid sequence of SEQ ID NO. 13 which further comprises at least one mutation, as compared to SEQ ID NO. 13, selected from the group consisting of:
(i) D12E, D29E, N59Q, N71Q, N71S, N71A, N86Q, N86S, D114E, D114S, N163S, N163Q, N259Q, N259S, and N259A,
(ii) V232I, D284M, D284Q, D284S, V308S, G311H, G311K, G311N, G311Q, and G311S, and
(iii) A290N, A290Q, A290K, H147S, H147T, H147N, H147Q, and D193N.
2. The polypeptide of claim 1 , wherein the at least one mutation is selected from the group consisting of N86Q, N86S, D114E, and D114S.
3. The polypeptide of claim 1 , wherein the at least one mutation is selected from the group consisting of:
i) D284M;
ii) D284M and G311S;
iii) D284M, V232I, and V308S;
iv)D284M, G311S, V232I, and V308S;
v) D284Q;
vi) D284Q and G311S;
vii) D284Q, V232I, and V308S;
viii) D284Q, G311S, V232I, and V308S;
ix) D284S and G311Q;
x) D284S, G311Q, V232I, and V308S;
xi) G311K;
xii) G311Q;
xiii) G311N;
xiv) G311S;
xv) G311H;
xvi) G311K, V232I, and V308S;
xvii) G311Q, V232I, and V308S;
xviii) G311N, V232I, and V308S;
xix) G311S, V232I, and V308S; and
XX) G311H, V232I, and V308S.
4. The polypeptide of claim 1 , wherein the at least one mutation is selected from the group consisting of:
i) A290N;
ii) A290Q;
iii) A290K;
iv) H147S;
v) H147T;
vi) H147N;
vii) H147Q;
viii) H147S and D193N;
ix) H147T and D193N;
x) H147N and D193N; or combinations thereof.