ISSN:
1573-5001
Keywords:
13C
;
chemical shifts
;
cysteine
;
disulfide bond
;
redox
Source:
Springer Online Journal Archives 1860-2000
Topics:
Biology
,
Chemistry and Pharmacology
Notes:
Abstract The presence of disulfide bonds can be detected unambiguously only by X-ray crystallography, and otherwise must be inferred by chemical methods. In this study we demonstrate that 13C NMR chemical shifts are diagnostic of disulfide bond formation, and can discriminate between cysteine in the reduced (free) and oxidized (disulfide bonded) state. A database of cysteine 13C Cα and Cβ chemical shifts was constructed from the BMRB and Sheffield databases, and published journals. Statistical analysis indicated that the Cβ shift is extremely sensitive to the redox state, and can predict the disulfide-bonded state. Further, chemical shifts in both states occupy distinct clusters as a function of secondary structure in the Cα/C β chemical shift map. On the basis of these results, we provide simple ground rules for predicting the redox state of cysteines; these rules could be used effectively in NMR structure determination, predicting new folds, and in protein folding studies.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1023/A:1008398416292
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