| Literature DB >> 24914408 |
Natalya Gertsik1, T Eric Ballard2, Christopher W Am Ende3, Douglas S Johnson4, Yue-Ming Li5.
Abstract
γ-Secretase undergoes endoproteolysis of its catalytic subunit, presenilin (PS), to form PS N-terminal and C-terminal fragments (PS1-NTF/CTF), which generate the active site. PS endoproteolysis, catalyzed by presenilinase (PSase), remains poorly understood and requires novel chemical approaches for its mechanistic study. CBAP is a dual inhibitor that suppresses both γ-secretase and PSase activities. To probe γ-secretase and PSase activity in cells, we have synthesized the clickable photoaffinity probe CBAP-BPyne. We found that CBAP-BPyne specifically labels PS1-NTF and signal peptide peptidase (SPP). CBAP-BPyne is a valuable tool to directly study the mechanism of endoproteolysis.Entities:
Year: 2014 PMID: 24914408 PMCID: PMC4048150 DOI: 10.1039/C3MD00281K
Source DB: PubMed Journal: Medchemcomm ISSN: 2040-2503 Impact factor: 3.597