Engineered botulinum neurotoxin

Patent metadata

Field	Value
Publication number	US-9598685-B2
Application number	US-201314403768-A
Country	US
Kind code	B2
Filing date	Mar 13, 2013
Priority date	May 30, 2012
Publication date	Mar 21, 2017
Grant date	Mar 21, 2017

Abstract

Disclosed herein are botulinum neurotoxin (BoNT) polypeptides with a modified receptor binding domain of Clostridial botulinum serotype B (B-H c ), comprising one or more substitution mutations corresponding to substitution mutations in serotype B, strain 1, V1118M; Y1183M; E1191M; E1191I; E1191Q; E1191T; S1199Y; S1199F; S1199L; SI 20 IV; or combinations thereof. Specific combination mutations include E1 191M and S1199L, E1191M and S1199Y, E1191M and S1199F, E1191Q and S1199L, E1191Q and S 1199Y, or E 1191 Q and S 1199F. Other substitution mutations are also disclosed. Isolated modified receptor binding domains, chimeric molecules, pharmaceutical compositions, and methods of using the same are also disclosed.

First claim

What is claimed:

1. A polypeptide comprising a modified receptor binding domain of Clostridial botulinum serotype B (B-H c ) comprising an amino acid substitution mutation at the amino acid position E1191 of the polypeptide of SEQ ID NO: 4 with M, Q, C, V, Y, T or I, wherein the substitution mutation produces enhanced binding of the modified B-H c to human SytII as compared to an identical molecule lacking the substitution mutation.

2. The polypeptide of claim 1 that is a botulinum neurotoxin (BoNT) polypeptide comprising:
a) a protease domain;
b) a protease cleavage site;
c) a translocation domain; and
d) the modified receptor binding domain of Clostridial botulinum serotype B (B-H c .

3. The polypeptide of claim 1 , further comprising one or more amino acid substitution mutations at an amino acid position of the SEQ ID NO: 4, selected from the group consisting of:
substitution of E, H, Y, W, F, or L at S1199;
substitution of Q, Y, A or S at W1178;
substitution of C, P, or M at Y1183;
substitution of S, M or Y at P1117;
substitution of V at S1201;
substitution of M at V1118;
substitution of Y at A1196;
substitution of M at Y1181; and combinations thereof.

4. The polypeptide of claim 1 , wherein the modified (B-H c ) comprises two substitution mutations.

5. The polypeptide of claim 4 wherein the two substitution mutations correspond to
E1191M and S1199Y;
E1191M and S1199W;
E1191M and S1199L;
E1191M and S1199Y;
E1191M and S1199F;
E1191Q and S1199Y;
E1191Q and S1199W;
E1191Q and S1199L;
E1191Q and S1199Y;
E1191Q and S1199F;
E1191C and S1199Y;
E1191C and S1199W;
E1191V and S1199Y;
E1191V and S1199W;
E1191M and W1178Q;
E1191Q and W1178Q;
E1191C and W1178Q; or
E1191V and W1178Q.

6. The polypeptide of claim 1 , wherein the substitution mutation is a non-naturally occurring amino acid.

7. The polypeptide of claim 1 , wherein the modified B-H c is of strain 1.

8. The polypeptide of claim 2 wherein the protease domain, translocation domain, and protease cleavage site are from serotype selected from the group consisting of A, B, C, D, E, F, G, and combinations thereof.

9. The polypeptide of claim 8 , wherein the protease domain, translocation domain, and protease cleavage site are from serotype B, strain 1.

10. The polypeptide of claim 8 , wherein the protease domain, translocation domain, and protease cleavage site are from serotype A, strain 1.

11. A composition comprising a botulinum neurotoxin polypeptide comprising a modified receptor binding domain of Clostridial botulinum serotype B (B-H c ) comprising an amino acid substitution mutation at the amino acid position E1191 of the polypeptide of SEQ ID NO: 4 with M, Q, C, V, Y, T or I, wherein the substitution mutation produces enhanced binding of the modified B-H c to human SytII as compared to an identical molecule lacking the substitution mutation.

12. The composition of claim 11 , wherein the modified receptor binding domain of Clostridial botulinum serotype B (B-H c ) further comprises one or more amino acid substitution mutations at an amino acid position of the SEQ ID NO: 4, selected from the group consisting of:
substitution of E, H, Y, W, F, or L at S1199;
substitution of Q, Y, A or S at W1178;
substitution of C, P, or M at Y1183;
substitution of S, M or Y at P1117;
substitution of V at S1201;
substitution of M at V1118;
substitution of Y at A1196;
substitution of M at Y1181; and combinations thereof.

13. The composition of claim 11 , wherein the modified (B-H c ) comprises two substitution mutations.

14. The composition of claim 13 wherein the two substitution mutations correspond to:
E1191M and S1199Y;
E1191M and S1199W;
E1191M and S1199L;
E1191M and S1199Y;
E1191M and S1199F;
E1191Q and S1199Y;
E1191Q and S1199W;
E1191Q and S1199L;
E1191Q and S1199Y;
E1191Q and S1199F;
E1191C and S1199Y;
E1191C and S1199W;
E1191V and S1199Y;
E1191V and S1199W;
E1191M and W1178Q;
E1191Q and W1178Q;
E1191C and W1178Q; or
E1191V and W1178Q.

15. A kit comprising a composition comprising a botulinum neurotoxin polypeptide comprising a modified receptor binding domain of Clostridial botulinum serotype B (B-H c ) comprising an amino acid substitution mutation at the amino acid position E1191 of the polypeptide of SEQ ID NO: 4 with M, Q, C, V, Y, T or I, wherein the substitution mutation produces enhanced binding of the modified B-H c to human SytII as compared to an identical molecule lacking the substitution mutation, and directions for therapeutic administration of the composition.

16. A chimeric molecule comprising a first portion that is the modified receptor binding domain of Clostridial botulinum serotype B (B-Hc) comprising an amino acid substitution mutation at the amino acid position E1191 of the polypeptide of SEQ ID NO: 4 with M, Q, C, V, Y, T or I linked to a second portion.

17. A composition comprising chimeric molecule comprising a first portion that is the modified receptor binding domain of Clostridial botulinum serotype B (B-Hc) comprising an amino acid substitution mutation at the amino acid position E1191 of the polypeptide of SEQ ID NO: 4 with M, Q, C, V, Y, T or I linked to a second portion.

18. A kit comprising a composition comprising chimeric molecule comprising a first portion that is the modified receptor binding domain of Clostridial botulinum serotype B (B-Hc) comprising an amino acid substitution mutation at the amino acid position E1191 of the polypeptide of SEQ ID NO: 4 with M, Q, C, V, Y, T or I linked to a second portion and directions for administration of the composition.

Assignees

• Harvard College

Inventors

• Dong Min
• Peng Lisheng
• Stenmark Pål Erik Gustav
• Berntsson Ronnie Per Arne

Classifications

• A61P43/00

  Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

• A61P25/04

  Centrally acting analgesics, e.g. opioids · CPC title

• A61P27/02

  Ophthalmic agents · CPC title

• A61P25/14

  for treating abnormal movements, e.g. chorea, dyskinesia · CPC title

• A61P25/08

  Antiepileptics; Anticonvulsants · CPC title