Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5407570 | Journal of Magnetic Resonance | 2006 | 7 Pages |
Abstract
The revisited version of the HACACO experiment here presented, is more robust and straightforward to implement and continues to be, to a greater extent, a convenient tool for protein backbone resonance assignment. Additionally, it turns out to be a sensitive and accurate method to measure Cα-Hα residual dipolar couplings (RDCs). The performance of our new pulse scheme for measurement of RDCs was tested on two proteins with different secondary structures: one characterized by a high β-sheet content, the second dominated by the presence of α-helices. In both examples the new method provided significantly more accurate data, compared to all previously published 3D techniques.
Related Topics
Physical Sciences and Engineering
Chemistry
Physical and Theoretical Chemistry
Authors
Daniel O. Cicero, Gian Marco Contessa, Maurizio Paci, Renzo Bazzo,