Endogenous and fluorescent sterols reveal the molecular basis for ligand selectivity of human sterol transporters.

IF 5 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Lipid Research Pub Date : 2024-12-31 DOI:10.1016/j.jlr.2024.100738
Laura Depta, Hogan P Bryce-Rogers, Nienke J Dekker, Anna Wiehl Bønke, Nicolò Camporese, Mingxing Qian, Yuanjian Xu, Douglas F Covey, Luca Laraia
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Abstract

Sterol transport proteins (STPs) play a pivotal role in cholesterol homeostasis and therefore are essential for healthy human physiology. Despite recent advances in dissecting functions of STPs in the human cell, there is still a significant knowledge gap regarding their specific biological functions and a lack of suitable selective probes for their study. Here, we profile fluorescent steroid-based probes across ten STPs, uncovering substantial differences in their selectivity, aiding the retrospective and prospective interpretation of biological results generated with those probes. These results guided the establishment of an STP screening panel combining diverse biophysical assays, enabling the evaluation of 42 steroid-based natural products and derivatives. Combining this with a thorough structural analysis revealed the molecular basis for STP-specific selectivity profiles, leading to the uncovering of several new potent and selective Aster-B inhibitors and supporting the role of this protein in steroidogenesis.

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内源性和荧光甾醇揭示了人类甾醇转运体的配体选择性的分子基础。
固醇转运蛋白(STPs)在胆固醇稳态中起着关键作用,因此对健康的人体生理至关重要。尽管近年来在解剖STPs在人类细胞中的功能方面取得了进展,但关于其特定的生物学功能仍然存在重大的知识差距,并且缺乏合适的选择性探针来研究它们。在这里,我们分析了10种stp中基于荧光类固醇的探针,揭示了它们在选择性上的实质性差异,有助于对这些探针产生的生物学结果进行回顾性和前瞻性解释。这些结果指导了STP筛选面板的建立,该筛选面板结合了多种生物物理分析,能够对42种基于类固醇的天然产物和衍生物进行评估。结合全面的结构分析,揭示了STP特异性选择性谱的分子基础,从而发现了几种新的有效和选择性的Aster-B抑制剂,并支持该蛋白在类固醇形成中的作用。
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来源期刊
Journal of Lipid Research
Journal of Lipid Research 生物-生化与分子生物学
CiteScore
11.10
自引率
4.60%
发文量
146
审稿时长
41 days
期刊介绍: The Journal of Lipid Research (JLR) publishes original articles and reviews in the broadly defined area of biological lipids. We encourage the submission of manuscripts relating to lipids, including those addressing problems in biochemistry, molecular biology, structural biology, cell biology, genetics, molecular medicine, clinical medicine and metabolism. Major criteria for acceptance of articles are new insights into mechanisms of lipid function and metabolism and/or genes regulating lipid metabolism along with sound primary experimental data. Interpretation of the data is the authors’ responsibility, and speculation should be labeled as such. Manuscripts that provide new ways of purifying, identifying and quantifying lipids are invited for the Methods section of the Journal. JLR encourages contributions from investigators in all countries, but articles must be submitted in clear and concise English.
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