| Literature DB >> 10382310 |
M Salzmann1, K Pervushin, G Wider, H Senn, K Wüthrich.
Abstract
The greatly improved sensitivity resulting from the use of TROSY during 15N evolution and amide proton acquisition enables the recording of HNCA spectra of large proteins with constant-time 13C alpha evolution. In [13C]-ct-[15N,1H]-TROSY-HNCA experiments with a 2H/13C/15N-labeled 110 kDa protein, 7,8-dihydroneopterin aldolase from Staphylococcus aureus, nearly all correlation peaks seen in the [15N,1H]-TROSY-HNCA spectrum were also detected. The improved resolution in the 13C dimension then enabled a significant number of sequential assignments that could not be obtained with [15N,1H]-TROSY-HNCA without [13C]-constant-time period.Entities:
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Year: 1999 PMID: 10382310 DOI: 10.1023/a:1008346931993
Source DB: PubMed Journal: J Biomol NMR ISSN: 0925-2738 Impact factor: 2.835