Multiprotease therapeutics for chronic pain
The invention includes Clostridial neurotoxin derivatives containing at least two light chain endopeptidase domains, and nucleic acids encoding such Clostridial neurotoxin derivatives. In preferred embodiments, the invention includes methods and compositions for the treatment of inflammatory disorders (such as arthritis); chronic pain, such as neuropathic pain and inflammatory pain through the use of such Clostridial neurotoxin derivatives, including those derived from an intact BoNT/A having an LC/E-derived endopeptidase joined to the LC/A endopeptidase.
1. A nucleic acid having a nucleotide sequence encoding a polypeptide having a Clostridium botulinum translocation activity, a Clostridium botulinum cell surface binding activity, a first Clostridium botulinum endopeptidase activity and a second Clostridium botulinum endopeptidase activity said nucleic acid sequence being derived from a Clostridium botulinum nucleotide sequence and comprising a single open reading frame encoding, in sequence from carboxy terminus to amino terminus:
a) a Clostridium botulinum -derived binding domain comprising an H CN subdomain and an H CC subdomain,
b) a Clostridium botulinum -derived translocation domain,
c) a Clostridium botulinum -derived first endopeptidase domain,
d) and a Clostridium botulinum -derived second endopeptidase domain different from said first endopeptidase domain,
wherein, upon expression, each of said first endopeptidase domain and said second endopeptidase domain has a different selective proteolytic activity against a SNARE protein, and wherein said first and second domains endopeptidase are proteolytically active and recognize different amino acid cleavage sites in a SNARE protein.
2. The nucleic acid of claim 1 wherein codons encoding each of the binding domain, the translocation domain, the first endopeptidase domain, and the second endopeptidase domain, are optimized for expression in a cell type selected from the group consisting of: a bacterial cell, a mammalian cell, a yeast cell and an insect cell.
3. The nucleic acid of claim 2 wherein the codons are optimized for expression in an E. coli bacterial cell.
4. The nucleic acid of claim 1 wherein at least two domains selected from the group consisting of the binding domain, the translocation domain, the first endopeptidase domain, and the second endopeptidase domain are encoded by nucleic acid sequences derived from different Clostridial neurotoxins or Clostridial neurotoxin subtypes selected from the group consisting of: BoNT/A, BoNT/B, BoNT/C1, BoNT/D, BoNT/E, BoNT/F, and BoNT/G.
5. The nucleic acid of claim 4 wherein the first endopeptidase domain and the second endopeptidase domain are encoded by nucleic acid sequences derived from different Clostridial neurotoxin or Clostridial neurotoxin subtypes independently selected from the group consisting of: BoNT/A, BoNT/B, BoNT/C1, BoNT/D, BoNT/E, BoNT/F, and BoNT/G.
6. The nucleic acid of claim 5 wherein the first endopeptidase domain is encoded by nucleic acid sequences derived from BoNT/A and said second endopeptidase domain is encoded by nucleic acid sequences derived from BoNT/C1.
7. The nucleic acid of claim 5 wherein the first endopeptidase domain is encoded by nucleic acid sequences derived from BoNT/A and said second endopeptidase domain is encoded by nucleic acid sequences derived from BoNT/E.
8. The nucleic acid of claim 7 wherein said open reading frame encodes at least six contiguous histidine residues located between the nucleotide sequence encoding said binding domain and the stop codon.
9. A nucleic acid having a nucleotide sequence encoding a polypeptide comprising a consisting of a Clostridium botulinum -derived neurotoxin, said nucleic acid sequence comprising a single open reading frame encoding, in sequence from carboxy terminus to amino terminus:
a) a binding domain comprising an H CN subdomain and an H CC subdomain,
b) a translocation domain,
c) a first endopeptidase domain,
d) and a second endopeptidase domain different from said first endopeptidase domain,
wherein, upon translation of said nucleic acid, said neurotoxin has greater analgesic activity against chronic pain than an otherwise identical neurotoxin in which one of said first or second endopeptidase is inactive as a protease.
10. The nucleic acid of claim 9 encoding a protease cleavage site located at a position between those regions encoding the translocation domain and the first endopeptidase domain.
11. The nucleic acid of claim 9 wherein each of said first endopeptidase domain and said second endopeptidase domain has a selective proteolytic activity against the SNARE protein SNAP-25, and recognizes a different amino acid cleavage site in SNAP-25.
12. The nucleic acid of claim 9 wherein the binding domain encoded by said nucleic acid comprises a BoNT neurotoxin Hc region.
13. The nucleic acid of claim 9 wherein the binding domain encoded by said nucleic acid lacks a complete BoNT neurotoxin Hc region.
14. The nucleic acid of claim 13 wherein the binding domain encoded by said nucleic acid comprises a functional BoNT H CN region.
15. The nucleic acid of claim 9 wherein the binding domain encoded by said nucleic acid comprises a non-Clostridial binding moiety.
16. The nucleic acid of claim 15 wherein the binding domain encoded by said nucleic acid comprises a BoNT neurotoxin Hc region.
17. The nucleic acid of claim 15 wherein the binding domain encoded by said nucleic acid lacks a complete neurotoxin BoNT Hc region.
18. The nucleic acid of claim 17 wherein the binding domain encoded by said nucleic acid comprises a functional BoNT H CN region.
19. The nucleic acid of claim 9 wherein the first endopeptidase domain and said second endopeptidase domain encoded by said nucleic acid are derived from different Clostridial neurotoxins and said first endopeptidase and said second endopeptidase are independently selected from the group consisting of an endopeptidase derived from: BoNT/A, BoNT/B, BoNT/C1, BoNT/D, BoNT/E, BoNT/F, BoNT/G.
20. The nucleic acid of claim 9 wherein the binding domain comprises a BoNT binding subdomain H CN and a binding subdomain H CC , and wherein binding subdomain H CN , binding subdomain H CC , and said translocation domain encoded by the nucleic acid are respectively independently derived from a naturally occurring BoNT binding subdomain H CN , a naturally occurring BoNT binding subdomain H CC , and a naturally occurring BoNT translocation domain, each from a Clostridial neurotoxin subtype selected from the group consisting of BoNT/A, BoNT/B, BoNT/C1, BoNT/D, BoNT/E, BoNT/F, BoNT/G.