Chaperone Spy Protects Outer Membrane Proteins from Folding Stress via Dynamic Complex Formation.

ABSTRACT: Gram-negative bacteria have a multicomponent and constitutively active periplasmic chaperone system to ensure the quality control of their outer membrane proteins (OMPs). Recently, OMPs have been identified as a new class of vulnerable targets for antibiotic development, and therefore a comprehensive understanding of OMP quality control network components will be critical for discovering antimicrobials. Here, we demonstrate that the periplasmic chaperone Spy protects certain OMPs against protein-unfolding stress and can functionally compensate for other periplasmic chaperones, namely Skp and FkpA, in the Escherichia coli K-12 MG1655 strain. After extensive in vivo genetic experiments for functional characterization of Spy, we use nuclear magnetic resonance and circular dichroism spe

SUBMITTER: He W 

PROVIDER: S-EPMC8546600 | biostudies-literature | 2021 Oct

REPOSITORIES: biostudies-literature