Breaking symmetry in the structure determination of (large) symmetric protein dimers.

Abstract:

:We demonstrate a novel methodology to disrupt the symmetry in the NMR spectra of homodimers. A paramagnetic probe is introduced sub-stoichiometrically to create an asymmetric system with the paramagnetic probe residing on only one monomer within the dimer. This creates sufficient magnetic anisotropy for resolution of symmetry-related overlapped resonances and, consequently, detection of pseudocontact shifts and residual dipolar couplings specific to each monomeric component. These pseudocontact shifts can be readily incorporated into existing structure refinement calculations and enable determination of monomer orientation within the dimeric protein. This methodology can be widely used for solution structure determination of symmetric dimers.

journal_name

J Biomol NMR

authors

Gaponenko V,Altieri AS,Li J,Byrd RA

doi

10.1023/a:1020948529076

subject

Has Abstract

pub_date

2002-10-01 00:00:00

pages

143-8

issue

2

eissn

0925-2738

issn

1573-5001

journal_volume

24

pub_type

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