| Literature DB >> 12149447 |
Chad M Rienstra1, Lisa Tucker-Kellogg, Christopher P Jaroniec, Morten Hohwy, Bernd Reif, Michael T McMahon, Bruce Tidor, Tomas Lozano-Pérez, Robert G Griffin.
Abstract
The three-dimensional structure of the chemotactic peptide N-formyl-l-Met-l-Leu-l-Phe-OH was determined by using solid-state NMR (SSNMR). The set of SSNMR data consisted of 16 (13)C-(15)N distances and 18 torsion angle constraints (on 10 angles), recorded from uniformly (13)C,(15)N- and (15)N-labeled samples. The peptide's structure was calculated by means of simulated annealing and a newly developed protocol that ensures that all of conformational space, consistent with the structural constraints, is searched completely. The result is a high-quality structure of a molecule that has thus far not been amenable to single-crystal diffraction studies. The extensions of the SSNMR techniques and computational methods to larger systems appear promising.Entities:
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Year: 2002 PMID: 12149447 PMCID: PMC124901 DOI: 10.1073/pnas.152346599
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205