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The Charge Distribution in the Cytoplasmic Loop of Subunit C of the F1F0 ATPase Is a Determinant for YidC Targeting

Authors :
Stefan Kol
Arnold J. M. Driessen
Nico Nouwen
Groningen Biomolecular Sciences and Biotechnology
Molecular Microbiology
Zernike Institute for Advanced Materials
Source :
The Journal of Biological Chemistry, 283(15), 9871-9877. AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
Publication Year :
2008
Publisher :
Elsevier BV, 2008.

Abstract

YidC is a member of the Oxa1 family of proteins that facilitates the membrane insertion of a subset of inner membrane proteins in Escherichia coli. YidC acts as an insertase for membrane insertion of subunit c of the F1F0 ATP synthase (F(0)c), but the requirements for substrate recognition have remained unclear. Here, we have analyzed the role of the charged aminoacyl residues in F(0)c in YidC targeting and membrane insertion. Binding experiments demonstrate that F(0)c is targeted directly to YidC without the presence of a stable lipid surface-bound intermediate. Positive charges in the cytoplasmic loop of F(0)c are important determinants for YidC binding and subsequent membrane insertion. These data support a model in which F(0)c binds directly to YidC prior to its membrane insertion.

Details

ISSN :
00219258
Volume :
283
Database :
OpenAIRE
Journal :
Journal of Biological Chemistry
Accession number :
edsair.doi.dedup.....708f8b4fb29c6bc129ac9da62c9172da