TRIM11 for degradation of protein aggregates
The present invention relates to compositions and methods for promoting the degradation of misfolded proteins and protein aggregates. The compositions and methods may be used to treat a disorder associated with misfolded proteins or protein aggregates. In certain instances, the compositions and methods relate to modulators of one or more TRIM proteins or one or more STUbLs.
1. A method of reducing protein aggregates associated with a disease or disorder in a subject in need thereof, the method comprising administering to the subject a composition comprising a nucleic acid sequence encoding human TRIM11, wherein the protein aggregates are selected from the group consisting of: ataxin-1 aggregates, huntingtin aggregates, alpha-synuclein aggregates, mutant p53 aggregates and beta-amyloid aggregates.
2. The method of claim 1 , wherein the disease or disorder comprises a neurodegenerative disease or disorder.
3. The method of claim 1 , wherein the method comprises administering the composition to at least one neural cell of the subject.
4. The method of claim 1 , wherein the composition comprises an adeno-associated viral (AAV) vector comprising a nucleic acid sequence encoding a peptide comprising human TRIM11.
5. The method of claim 4 , wherein the AAV vector comprises an AAV9 vector.
6. A method comprising administering to a subject having a disease or disorder a composition comprising a nucleic acid sequence encoding human TRIM11, wherein:
a) the subject has Alzheimer's disease and wherein the method reduces the level of beta-amyloid aggregates in the subject;
b) the subject has Parkinson's disease and wherein the method reduces the level of alpha-synuclein aggregates in the subject;
c) the subject has spinocerebellar ataxia and wherein the method reduces the level of ataxin-1 aggregates in the subject;
d) the subject has Huntington's disease and wherein the method reduces the level of huntingtin aggregates in the subject; or
e) the subject has cancer associated with mutant p53 and wherein the method reduces the level of mutant p53 aggregates in the subject.
7. The method of claim 6 , wherein the method comprises administering the composition to at least one neural cell of the subject.
8. The method of claim 6 , wherein the composition comprises an adeno-associated viral (AAV) vector comprising a nucleic acid sequence encoding a peptide comprising human TRIM11.
9. The method of claim 8 , wherein the AAV vector comprises an AAV9 vector.