Velander Paul, Wu Ling, Ray W Keith, Helm Richard F, Xu Bin
Department of Biochemistry, ‡Center for Drug Discovery, and §Translational Obesity Research Center, Virginia Polytechnic Institute & State University , Blacksburg, Virginia 24061, United States.
Biochemistry. 2016 Aug 9;55(31):4255-8. doi: 10.1021/acs.biochem.6b00578. Epub 2016 Jul 27.
Amyloid formation of the 37-residue amylin is involved in the pathogenesis of type 2 diabetes and, potentially, diabetes-induced neurological deficits. Numerous flavonoids exhibit inhibitory effects against amylin amyloidosis, but the mechanisms of inhibition remain unclear. Screening a library of natural compounds uncovered a potent lead compound, the flavone baicalein. Baicalein inhibits amylin amyloid formation and reduces amylin-induced cytotoxicity. Analogue analyses demonstrated, for the first time, key roles of the vicinal hydroxyl groups on the A-ring. We provided mass spectrometric evidence that incubating baicalein and amylin leads to their conjugation, consistent with a Schiff base mechanism.
由37个氨基酸残基组成的胰岛淀粉样多肽的淀粉样形成与2型糖尿病的发病机制有关,并且可能与糖尿病引起的神经功能缺损有关。许多黄酮类化合物对胰岛淀粉样多肽淀粉样变性具有抑制作用,但其抑制机制尚不清楚。通过筛选天然化合物文库发现了一种有效的先导化合物——黄酮黄芩素。黄芩素可抑制胰岛淀粉样多肽的淀粉样形成并降低其诱导的细胞毒性。类似物分析首次证明了A环上邻位羟基的关键作用。我们提供了质谱证据,表明黄芩素与胰岛淀粉样多肽孵育会导致它们结合,这与席夫碱机制一致。