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线粒体丙酮酸载体的 50 年:对其结构、功能和抑制的新见解。

Fifty years of the mitochondrial pyruvate carrier: New insights into its structure, function, and inhibition.

机构信息

Medical Research Council Mitochondrial Biology Unit, University of Cambridge, Cambridge, UK.

出版信息

Acta Physiol (Oxf). 2023 Aug;238(4):e14016. doi: 10.1111/apha.14016. Epub 2023 Jun 27.

Abstract

The mitochondrial pyruvate carrier (MPC) resides in the mitochondrial inner membrane, where it links cytosolic and mitochondrial metabolism by transporting pyruvate produced in glycolysis into the mitochondrial matrix. Due to its central metabolic role, it has been proposed as a potential drug target for diabetes, non-alcoholic fatty liver disease, neurodegeneration, and cancers relying on mitochondrial metabolism. Little is known about the structure and mechanism of MPC, as the proteins involved were only identified a decade ago and technical difficulties concerning their purification and stability have hindered progress in functional and structural analyses. The functional unit of MPC is a hetero-dimer comprising two small homologous membrane proteins, MPC1/MPC2 in humans, with the alternative complex MPC1L/MPC2 forming in the testis, but MPC proteins are found throughout the tree of life. The predicted topology of each protomer consists of an amphipathic helix followed by three transmembrane helices. An increasing number of inhibitors are being identified, expanding MPC pharmacology and providing insights into the inhibitory mechanism. Here, we provide critical insights on the composition, structure, and function of the complex and we summarize the different classes of small molecule inhibitors and their potential in therapeutics.

摘要

线粒体丙酮酸载体(MPC)位于线粒体的内膜上,通过将糖酵解产生的丙酮酸从细胞质转运到线粒体基质中,将细胞质和线粒体代谢联系起来。由于其在代谢中的核心作用,它已被提议作为治疗糖尿病、非酒精性脂肪肝、神经退行性疾病和依赖线粒体代谢的癌症的潜在药物靶点。由于涉及的蛋白质仅在十年前才被鉴定出来,并且其纯化和稳定性方面的技术困难阻碍了功能和结构分析的进展,因此人们对 MPC 的结构和机制知之甚少。MPC 的功能单位是由两个小的同源膜蛋白组成的异二聚体,在人类中为 MPC1/MPC2,在睾丸中形成替代复合物 MPC1L/MPC2,但 MPC 蛋白存在于生命之树的各个分支中。每个单体的预测拓扑结构由一个两亲性螺旋 followed by 三个跨膜螺旋组成。越来越多的抑制剂正在被鉴定出来,这扩大了 MPC 的药理学,并为抑制机制提供了深入的了解。在这里,我们提供了对该复合物的组成、结构和功能的关键见解,并总结了不同类别的小分子抑制剂及其在治疗中的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1607/10909473/92ef871ab2d2/APHA-238-e14016-g038.jpg

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