Department of Radiology, Perelman School of Medicine , University of Pennsylvania , Philadelphia , Pennsylvania 19104 , United States.
Department of Chemistry , University of Pennsylvania , Philadelphia , Pennsylvania 19104 , United States.
ACS Chem Neurosci. 2018 Nov 21;9(11):2521-2527. doi: 10.1021/acschemneuro.8b00177. Epub 2018 May 16.
The fibrillary aggregation of the protein alpha synuclein (Asyn) is a hallmark of Parkinson's disease, and the identification of small molecule binding sites on fibrils is essential to the development of diagnostic imaging probes. A series of molecular modeling, photoaffinity labeling, mass spectrometry, and radioligand binding studies were conducted on Asyn fibrils. The results of these studies revealed the presence of three different binding sites within fibrillar Asyn capable of binding small molecules with moderate to high affinity. A knowledge of the amino acid residues in these binding sites will be important in the design of high affinity probes capable of imaging fibrillary species of Asyn.
蛋白质 α-突触核蛋白(Asyn)的纤维状聚集是帕金森病的一个标志,鉴定纤维上的小分子结合位点对于开发诊断成像探针至关重要。对 Asyn 纤维进行了一系列分子建模、光亲和标记、质谱和放射性配体结合研究。这些研究的结果表明,纤维状 Asyn 中存在三个不同的结合位点,能够与具有中等至高亲和力的小分子结合。这些结合位点中的氨基酸残基的知识对于设计能够成像 Asyn 纤维状的高亲和力探针将非常重要。