| Literature DB >> 18410104 |
Vitali Sikirzhytski1, Natalya I Topilina, Seiichiro Higashiya, John T Welch, Igor K Lednev.
Abstract
Elucidating the structure of the cross-beta core in large amyloid fibrils is a challenging problem in modern structural biology. For the first time, a set of de novo polypeptides was genetically engineered to form amyloid-like fibrils with similar morphology and yet different strand length. Differential ultraviolet Raman spectroscopy allowed for separation of the spectroscopic signatures of the highly ordered beta-sheet strands and turns of the fibril core. The relationship between Raman frequencies and Ramachandran dihedral angles of the polypeptide backbone indicates the nature of the beta-sheet and turn structural elements.Mesh:
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Year: 2008 PMID: 18410104 DOI: 10.1021/ja8006275
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419