期刊
JOURNAL OF MAGNETIC RESONANCE
卷 164, 期 1, 页码 92-103出版社
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/S1090-7807(03)00083-1
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资金
- NCRR NIH HHS [RR-00995] Funding Source: Medline
- NIGMS NIH HHS [GM-23403] Funding Source: Medline
The solid state NMR technique of rotational resonance (R-2) has been used extensively to measure distances approaching 5-6 Angstrom between C-13 nuclei in a variety of compounds including amyloidogenic peptides and membrane proteins. The accuracy of the distance information extracted from the time-dependent spin dynamics at R-2 is often limited by the accuracy with which the relevant zero-quantum lineshape parameters are estimated. Here we demonstrate that measurement of spinning frequency dependent magnetization exchange dynamics provides data from which both distance and zero-quantum relaxation parameters can be extracted independently. In addition to providing more accurate distance information, this technique allows examination of the zero-quantum lineshape, which can indicate the presence of correlated relaxation or chemical shift distributions between dipolar-coupled sites. With this approach we have separated the contribution of dipolar couplings and zero quantum relaxation to R-2 exchange curves. Thus, we have significantly improved the accuracy of the measurement of the intramolecular, internuclear distances between a pair of C-13's in two model compounds (N-acetyl-D,L-valine and glycylglycine . HCl) that lie in the distance range 4.6-4.7 Angstrom (C) 2003 Elsevier Inc. All rights reserved.
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