Constructs for delivery of therapeutic agents to neuronal cells
A non-toxic polypeptide, for delivery of a therapeutic agent to a neuronal cell, comprises a binding domain that binds to the neuronal cell, and a translocation domain that translocates the therapeutic agent into the neuronal cell, wherein the translocation domain is not a H N domain of a clostridial toxin and is not a fragment or derivative of a H N domain of a clostridial toxin.
1 . A composition comprising a therapeutic agent linked to a non-toxic delivery polypeptide, wherein the delivery polypeptide is for delivery of said therapeutic agent to a neuronal cell, said delivery polypeptide comprising:
(a) a binding domain that binds to the neuronal cell, and
(b) a translocation domain that translocates the therapeutic agent into the neuronal cell; and
wherein the therapeutic agent is an anti-SNARE protein antibody.
2 . A composition according to claim 1 , wherein the translocation domain is a non-aggregating translocation domain as measured by size in physiological buffers.
3 . A composition according to claim 1 , wherein the translocation domain is selected from (1) a H N domain of a diphtheria toxin, (2) a fragment or derivative of (1) that substantially retains the translocating activity of the H N domain of a diphtheria toxin, (3) a fusogenic peptide, (4) a membrane disrupting peptide, and (5) translocating fragments and derivatives of (3) and (4).
4 . A composition according to claim 1 , wherein the delivery polypeptide has the binding specificity of tetanus toxin and reduced affinity to neutralising antibodies to tetanus toxin compared with the affinity to such antibodies of native tetanus toxin heavy chain.
5 . A composition according to claim 1 , wherein the translocation domain is not a H N domain of a clostridial toxin and is not a fragment or derivative of a H N domain of a clostridial toxin.
6 . A composition according to claim 1 , wherein the delivery polypeptide has reduced affinity to neutralising antibodies to tetanus toxin compared with the affinity to such antibodies of native tetanus toxin heavy chain.
7 . A composition according to any previous claim wherein the binding domain comprises a botulinum H C domain.
8 . A composition according to claim 1 , wherein the binding domain comprises a tetanus H C domain.
9 . A composition according to claim 1 , wherein the binding domain comprises a hybrid of a botulinum H C domain and a tetanus H C domain.
10 . A composition according to claim 1 , wherein said delivery polypeptide comprises a tetanus H C domain and a diphtheria H N domain.
11 . A composition according to claim 1 , wherein said delivery polypeptide comprises a botulinum H C domain and diphtheria H N domain.
12 . A composition according to claim 1 ., wherein the therapeutic substance is chemically bound to said polypeptide.
13 . A composition according to claim 1 , wherein the therapeutic substance is linked to a translocation domain of said polypeptide.
14 . A composition according to claim 1 , wherein the therapeutic agent is produced as a fusion protein by recombinant technology.