Efficient cellular solid-state NMR of membrane proteins by targeted protein labeling.

Abstract:

:Solid-state NMR spectroscopy (ssNMR) has made significant progress towards the study of membrane proteins in their native cellular membranes. However, reduced spectroscopic sensitivity and high background signal levels can complicate these experiments. Here, we describe a method for ssNMR to specifically label a single protein by repressing endogenous protein expression with rifampicin. Our results demonstrate that treatment of E. coli with rifampicin during induction of recombinant membrane protein expression reduces background signals for different expression levels and improves sensitivity in cellular membrane samples. Further, the method reduces the amount of time and resources needed to produce membrane protein samples, enabling new strategies for studying challenging membrane proteins by ssNMR.

journal_name

J Biomol NMR

authors

Baker LA,Daniëls M,van der Cruijsen EA,Folkers GE,Baldus M

doi

10.1007/s10858-015-9936-5

subject

Has Abstract

pub_date

2015-06-01 00:00:00

pages

199-208

issue

2

eissn

0925-2738

issn

1573-5001

journal_volume

62

pub_type

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