Methods and compositions for detecting amyotrophic lateral sclerosis
View Patent ↗The invention provides binding proteins that bind to misfolded or monomeric SOD1, and not to native homodimeric SOD1. The invention also includes methods of diagnosing, detecting or monitoring amyotrophic lateral sclerosis in a subject. In addition, the invention provides methods of identifying substances for the treatment or prevention of amyotrophic lateral sclerosis and kits using the binding proteins of the invention.
1. A method of detecting or monitoring familial amyotrophic lateral sclerosis in a subject having or suspected of having amyotrophic lateral sclerosis, comprising contacting a sample comprising motor neuron cells from the subject with an antibody or binding fragment thereof that binds to SEQ ID NO:1 in misfolded or monomeric SOD1, wherein familial amyotrophic lateral sclerosis is indicated if the antibody or binding fragment thereof binds to SEQ ID NO:1 in a misfolded or monomeric SOD1 in the sample.
2. The method according to claim 1 , wherein the sample comprises cerebrospinal fluid, spinal cord tissue, brain cells, a portion of the dorsal horn.
3. The method of claim 2 wherein the sample comprises a mitochondrial and/or microsomal enriched fraction.
4. The method according to claim 1 , wherein flow cytometry, Western blot, ELISA, or immunoprecipitation followed by SDS-PAGE immunocytochemistry is used to detect binding of the antibody or binding fragment thereof to misfolded or monomeric SOD1.
5. The method according to claim 1 , wherein the antibody or binding fragment thereof binds to an epitope on the dimer interface of SOD1.
6. The method according to claim 1 , wherein the antibody or binding fragment thereof is an antibody.
7. The method according to claim 6 , wherein the antibody is a monoclonal antibody.
8. The method according to claim 1 , wherein the antibody or binding fragment thereof is labeled with a detectable marker.