Department of Chemistry and Biochemistry, University of California, San Diego, 9500 Gilman Drive, La Jolla, California 92093-0358, USA.
Chem Commun (Camb). 2018 Aug 14;54(66):9107-9118. doi: 10.1039/c8cc03619e.
Advances in diagnostic medicine have led to an increased awareness and heightened concern for the high prevalence of amyloid-associated neurodegenerative diseases, especially in the elderly. These diseases have characteristic late stage symptoms that often make it possible to distinguish one disorder from another, though methods to diagnose neurodegeneration pre-symptomatically remain a critical challenge. At the molecular level, misfolded protein aggregates known as amyloids are ubiquitously found in many neurodegenerative diseases, and have been suggested to appear before clinical symptoms manifest. Amyloids have, thus, become a valuable potential diagnostic target for chemists, and recent work by many groups have shown that they can be selectively targeted by small molecule fluorescent probes. Here, we summarize some of the exciting work currently under investigation in the area of fluorescence-based amyloid detection and highlight recent efforts to expand the utility of amyloid-targeting fluorophores as clinical tools for disease diagnostics.
诊断医学的进步使得人们对淀粉样相关神经退行性疾病(尤其是在老年人中)的高发病率有了更高的认识和更强烈的关注。这些疾病具有特征性的晚期症状,这通常使得一种疾病与另一种疾病之间可以区分开来,尽管预症状诊断神经退行性变的方法仍然是一个关键挑战。在分子水平上,被称为淀粉样蛋白的错误折叠蛋白聚集体在许多神经退行性疾病中普遍存在,并被认为在临床症状出现之前出现。因此,淀粉样蛋白已成为化学家的一个有价值的潜在诊断靶点,许多研究小组的最新研究表明,它们可以被小分子荧光探针选择性地靶向。在这里,我们总结了当前在基于荧光的淀粉样检测领域中正在进行的一些令人兴奋的工作,并强调了最近为扩大淀粉样蛋白靶向荧光团的效用而做出的努力,将其作为疾病诊断的临床工具。