| Literature DB >> 16604425 |
Hideo Takahashi1, Mayumi Miyazawa, Yasuo Ina, Yoshifumi Fukunishi, Yumiko Mizukoshi, Haruki Nakamura, Ichio Shimada.
Abstract
Cross-saturation experiments allow the identification of the contact residues of large protein complexes (MW>50 K) more rigorously than conventional NMR approaches which involve chemical shift perturbations and hydrogen-deuterium exchange experiments [Takahashi et al. (2000) Nat. Struct. Biol., 7, 220-223]. In the amide proton-based cross-saturation experiment, the combined use of high deuteration levels for non-exchangeable protons of the ligand protein and a solvent with a low concentration of (1)H(2)O greatly enhanced the selectivity of the intermolecular cross-saturation phenomenon. Unfortunately, experimental limitations caused losses in sensitivity. Furthermore, since main chain amide protons are not generally exposed to solvent, the efficiency of the saturation transfer directed to the main chain amide protons is not very high. Here we propose an alternative cross-saturation experiment which utilizes the methyl protons of the side chains of the ligand protein. Owing to the fast internal rotation along the methyl axis, we theoretically and experimentally demonstrated the enhanced efficiency of this approach. The methyl-utilizing cross-saturation experiment has clear advantages in sensitivity and saturation transfer efficiency over the amide proton-based approach.Entities:
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Year: 2006 PMID: 16604425 DOI: 10.1007/s10858-006-0008-8
Source DB: PubMed Journal: J Biomol NMR ISSN: 0925-2738 Impact factor: 2.582