On the origin of NMR dipolar waves in transient helical elements of partially folded proteins

被引:29
作者
Jensen, Malene Ringkjobing [1 ]
Blackledge, Martin [1 ]
机构
[1] Inst Biol Struct Jean Pierre Ebel, CEA, CNRS, Prot Dynam & Fiexibil NMR,UJF UMR 5075, F-38027 Grenoble, France
关键词
D O I
10.1021/ja8039184
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The presence of dipolar coupling waves within helical elements of proteins implies an effective tilt of the main axis of the helical element relative to the magnetic field. Here, we investigate the origin of dipolar waves observed in helical elements of partially folded proteins. We find that the dipolar waves result from an effective tilt of the helix relative to the alignment axis that is determined by the directionality of the unfolded chains projected from the helix caps. The amplitude and phase of the dipolar wave depend in a predictable way on helix length. providing direct insight into helix stability, nucleation, and fraying in partially folded proteins.
引用
收藏
页码:11266 / +
页数:3
相关论文
共 17 条
[1]   Structure and disorder in the ribonuclease S-peptide probed by NMR residual dipolar couplings [J].
Alexandrescu, AT ;
Kammerer, RA .
PROTEIN SCIENCE, 2003, 12 (10) :2132-2140
[2]   Defining long-range order and local disorder in native α-synuclein using residual dipolar couplings [J].
Bernadó, P ;
Bertoncini, CW ;
Griesinger, C ;
Zweckstetter, M ;
Blackledge, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (51) :17968-17969
[3]   A structural model for unfolded proteins from residual dipolar couplings and small-angle x-ray scattering [J].
Bernadó, P ;
Blanchard, L ;
Timmins, P ;
Marion, D ;
Ruigrok, RWH ;
Blackledge, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (47) :17002-17007
[4]   Short-range, long-range and transition state interactions in the denatured state of ACBP from residual dipolar couplings [J].
Fieber, W ;
Kristjansdottir, S ;
Poulsen, FM .
JOURNAL OF MOLECULAR BIOLOGY, 2004, 339 (05) :1191-1199
[5]   Quantitative conformational analysis of partially folded proteins from residual dipolar couplings: Application to the molecular recognition element of Sendai virus nucleoprotein [J].
Jensen, Malene Ringkjobing ;
Houben, Klaartje ;
Lescop, Ewen ;
Blanchard, Laurence ;
Ruigrok, Rob W. H. ;
Blackledge, Martin .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (25) :8055-8061
[6]   Statistical coil model of the unfolded state: Resolving the reconciliation problem [J].
Jha, AK ;
Colubri, A ;
Freed, KF ;
Sosnick, TR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (37) :13099-13104
[7]   A solid-state NMR index of helical membrane protein structure and topology [J].
Marassi, FM ;
Opella, SJ .
JOURNAL OF MAGNETIC RESONANCE, 2000, 144 (01) :150-155
[8]   Theoretical analysis of residual dipolar coupling patterns in regular secondary structures of proteins [J].
Mascioni, A ;
Veglia, G .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (41) :12520-12526
[9]   Conformational distributions of unfolded polypeptides from novel NMR techniques [J].
Meier, Sebastian ;
Blackledge, Martin ;
Grzesiek, Stephan .
JOURNAL OF CHEMICAL PHYSICS, 2008, 128 (05)
[10]   Mapping the conformational landscape of urea-denatured ubiquitin using residual dipolar couplings [J].
Meier, Sebastian ;
Grzesiek, Stephan ;
Blackledge, Martin .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (31) :9799-9807