Sikirzhytski Vitali, Topilina Natalya I, Higashiya Seiichiro, Welch John T, Lednev Igor K
Department of Chemistry, University at Albany, SUNY, 1400 Washington Avenue, Albany, New York 12222, USA.
J Am Chem Soc. 2008 May 7;130(18):5852-3. doi: 10.1021/ja8006275. Epub 2008 Apr 15.
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.
阐明大型淀粉样纤维中交叉β核心的结构是现代结构生物学中的一个具有挑战性的问题。首次通过基因工程设计了一组从头合成的多肽,以形成具有相似形态但链长不同的淀粉样纤维。差分紫外拉曼光谱能够分离出高度有序的β折叠链和纤维核心转角的光谱特征。多肽主链的拉曼频率与拉马钱德兰二面角之间的关系表明了β折叠和转角结构元件的性质。