Structure-based drug design for TSPO: Challenges and opportunities

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
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引用次数: 0

Abstract

The translocator protein 18 kDa (TSPO) is an evolutionarily conserved mitochondrial transmembrane protein implicated in various neuropathologies and inflammatory conditions, making it a longstanding diagnostic and therapeutic target of interest. Despite the development of various classes of TSPO ligand chemotypes, and the elucidation of bacterial and non-human mammalian experimental structures, many unknowns exist surrounding its differential structural and functional features in health and disease. There are several limitations associated with currently used computational methodologies for modelling the native structure and ligand-binding behaviour of this enigmatic protein. In this perspective, we provide a critical analysis of the developments in the uses of these methods, outlining their uses, inherent limitations, and continuing challenges. We offer suggestions of unexplored opportunities that exist in the use of computational methodologies which offer promise for enhancing our understanding of the TSPO.

Abstract Image

Abstract Image

针对 TSPO 的基于结构的药物设计:挑战与机遇。
转运蛋白 18 kDa(TSPO)是一种进化保守的线粒体跨膜蛋白,与各种神经病变和炎症有关,因此长期以来一直是人们关注的诊断和治疗靶标。尽管开发了各种类型的 TSPO 配体化学型,并阐明了细菌和非人类哺乳动物的实验结构,但围绕其在健康和疾病中的不同结构和功能特征仍存在许多未知数。目前使用的计算方法在模拟这种神秘蛋白质的原生结构和配体结合行为方面存在一些局限性。在这篇论文中,我们对这些方法的使用发展进行了批判性分析,概述了它们的用途、固有局限性和持续挑战。我们提出了一些建议,说明在使用计算方法方面还存在哪些尚未开发的机会,这些机会有望增进我们对 TSPO 的了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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