期刊
PROTEIN ENGINEERING
卷 16, 期 6, 页码 429-434出版社
OXFORD UNIV PRESS
DOI: 10.1093/protein/gzg051
关键词
calcium binding; calmodulin; CD2.D1; EF-hand protein; FRET
资金
- NIGMS NIH HHS [GM 62999-1] Funding Source: Medline
The EF-hand calcium-binding loop III from calmodulin was inserted with glycine linkers into the scaffold protein CD2.D1 at three locations to study site-specific calcium binding properties of EF-hand motifs. After insertion, the host protein retains its native structure and forms a 1:1 metal-protein complex for calcium and its analog, lanthanum. Tyrosine-sensitized Tb3+ energy transfer exhibits metal binding and La3+ and Ca2+ compete for the metal binding site. The grafted EF-loop III in different environments has similar La3+ binding affinities, suggesting that it is largely solvated and functions independently from the host protein.
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