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CLiB——一种通过数据驱动筛选分离出的新型心磷脂结合剂。

CLiB - a novel cardiolipin-binder isolated data-driven and screening.

作者信息

Kleinwächter Isabel, Mohr Bernadette, Joppe Aljoscha, Hellmann Nadja, Bereau Tristan, Osiewacz Heinz D, Schneider Dirk

机构信息

Department of Chemistry, Biochemistry, Johannes Gutenberg University Mainz Hanns-Dieter-Hüsch-Weg 17 55128 Mainz Germany

Van 't Hoff Institute for Molecular Sciences and Informatics Institute, University of Amsterdam Amsterdam The Netherlands.

出版信息

RSC Chem Biol. 2022 Jun 10;3(7):941-954. doi: 10.1039/d2cb00125j. eCollection 2022 Jul 6.

Abstract

Cardiolipin, the mitochondria marker lipid, is crucially involved in stabilizing the inner mitochondrial membrane and is vital for the activity of mitochondrial proteins and protein complexes. Directly targeting cardiolipin by a chemical-biology approach and thereby altering the cellular concentration of "available" cardiolipin eventually allows to systematically study the dependence of cellular processes on cardiolipin availability. In the present study, physics-based coarse-grained free energy calculations allowed us to identify the physical and chemical properties indicative of cardiolipin selectivity and to apply these to screen a compound database for putative cardiolipin-binders. The membrane binding properties of the 22 most promising molecules identified in the approach were screened , using model membrane systems finally resulting in the identification of a single molecule, CLiB (CardioLipin-Binder). CLiB clearly affects respiration of cardiolipin-containing intact bacterial cells as well as of isolated mitochondria. Thus, the structure and function of mitochondrial membranes and membrane proteins might be (indirectly) targeted and controlled by CLiB for basic research and, potentially, also for therapeutic purposes.

摘要

心磷脂是线粒体标志性脂质,在稳定线粒体内膜方面起着关键作用,对线粒体蛋白质和蛋白质复合物的活性至关重要。通过化学生物学方法直接靶向心磷脂,从而改变“可利用”心磷脂的细胞浓度,最终能够系统地研究细胞过程对心磷脂可利用性的依赖性。在本研究中,基于物理的粗粒度自由能计算使我们能够确定指示心磷脂选择性的物理和化学性质,并将其应用于筛选化合物数据库以寻找假定的心磷脂结合剂。使用模型膜系统筛选了在该方法中鉴定出的22种最有前景的分子的膜结合特性,最终鉴定出一种单一分子CLiB(心磷脂结合剂)。CLiB明显影响含心磷脂的完整细菌细胞以及分离的线粒体的呼吸作用。因此,线粒体膜和膜蛋白的结构与功能可能会被CLiB(间接)靶向和控制,用于基础研究,也可能用于治疗目的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36f5/9257654/40d3bd4cd9d8/d2cb00125j-f1.jpg

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