A synthetic peptide corresponding to a region of the human pericentriolar material 1 (PCM-1) protein binds β-amyloid (Aβ1-42 ) oligomers.
JOURNAL OF NEUROCHEMISTRY(2013)
Abstract
We have recently reported that a similar to 19-kDa polypeptide, rPK-4, is a protein kinase Cs inhibitor that is 89% homologous to the 1171-1323 amino acid region of the 228-kDa human pericentriolar material-1 (PCM-1) protein (Chakravarthy etal. 2012). We have now discovered that rPK-4 binds oligomeric amyloid- peptide (A)(1-42) with high affinity. Most importantly, a PCM-1-selective antibody co-precipitated A and amyloid precursor protein (APP) from cerebral cortices and hippocampi from AD (Alzheimer's disease) transgenic mice that produce human APP and A(1-42), suggesting that PCM-1 may interact with amyloid precursor protein/A in vivo. We have identified rPK-4s A-binding domain using a set of overlapping synthetic peptides. We have found with ELISA, dot-blot, and polyacrylamide gel electrophoresis techniques that a similar to 5kDa synthetic peptide, amyloid binding peptide (ABP)-p4-5 binds A(1-42) at nM levels. Most importantly, ABP-p4-5, like rPK-4, appears to preferentially bind A(1-42) oligomers, believed to be the toxic AD-drivers. As expected from these observations, ABP-p4-5 prevented A(1-42) from killing human SH-SY5Y neuroblastoma cells via apoptosis. These findings indicate that ABP-p4-5 is a possible candidate therapeutic for AD.
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Key words
Alzheimer's disease,A(1-42) oligomers,A-binding peptides,PCM-1 protein
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