| Literature DB >> 3552643 |
H Senn, A Eugster, G Otting, F Suter, K Wüthrich.
Abstract
The salmonella phage P22 c2 repressor was produced with 90% 15N isotope labeling of all leucines, using the expression system E. coli W3110 lac IQ¿P 125. The N-terminal DNA-binding domain 1-76 was obtained by chymotrypsin cleavage. Its characterization by biochemical techniques, mass spectrometry, and one- and two-dimensional nuclear magnetic resonance (NMR) showed that highly residue-selective isotope labeling was achieved with the minimal growth medium used. The ability to obtain such isotope labeling opens new avenues for NMR studies of protein-DNA interactions in the P22 operator system.Entities:
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Year: 1987 PMID: 3552643 DOI: 10.1007/BF00254895
Source DB: PubMed Journal: Eur Biophys J ISSN: 0175-7571 Impact factor: 1.733