Sora Valentina, Papaleo Elena
Cancer Structural Biology, Danish Cancer Society Research Center, Copenhagen, Denmark.
Cancer Systems Biology, Section for Bioinformatics, Department of Health and Technology, Technical University of Denmark, Kongens Lyngby, Denmark.
Front Mol Biosci. 2022 May 24;9:864874. doi: 10.3389/fmolb.2022.864874. eCollection 2022.
Apoptosis is a mechanism of programmed cell death crucial in organism development, maintenance of tissue homeostasis, and several pathogenic processes. The B cell lymphoma 2 (BCL2) protein family lies at the core of the apoptotic process, and the delicate balance between its pro- and anti-apoptotic members ultimately decides the cell fate. BCL2 proteins can bind with each other and several other biological partners through the BCL2 homology domain 3 (BH3), which has been also classified as a possible Short Linear Motif and whose distinctive features remain elusive even after decades of studies. Here, we aim to provide an updated overview of the structural features characterizing BH3s and BH3-mediated interactions (with a focus on human proteins), elaborating on the plasticity of BCL2 proteins and the motif properties. We also discussed the implication of these findings for the discovery of interactors of the BH3-binding groove of BCL2 proteins and the design of mimetics for therapeutic purposes.
细胞凋亡是一种程序性细胞死亡机制,在生物体发育、组织稳态维持以及多种致病过程中至关重要。B细胞淋巴瘤2(BCL2)蛋白家族处于细胞凋亡过程的核心,其促凋亡和抗凋亡成员之间的微妙平衡最终决定细胞命运。BCL2蛋白可通过BCL2同源结构域3(BH3)相互结合以及与其他几个生物学伙伴结合,BH3也被归类为一种可能的短线性基序,即使经过数十年研究,其独特特征仍不清楚。在此,我们旨在提供关于表征BH3及其介导的相互作用的结构特征的最新概述(重点关注人类蛋白质),阐述BCL2蛋白的可塑性和基序特性。我们还讨论了这些发现对于发现BCL2蛋白BH3结合凹槽的相互作用分子以及设计治疗用模拟物的意义。