Department of Genetics, Stanford University, Stanford, CA, USA.
IUBMB Life. 2013 Jan;65(1):2-8. doi: 10.1002/iub.1111. Epub 2012 Dec 7.
Cell signaling is extensively wired between cellular components to sustain cell proliferation, differentiation, and adaptation. The interaction network is often manifested in how protein function is regulated through interacting with other cellular components including small molecule metabolites. While many biochemical interactions have been established as reactions between protein enzymes and their substrates and products, much less is known at the system level about how small metabolites regulate protein functions through allosteric binding. In the past decade, study of protein-small molecule interactions has been lagging behind other types of interactions. Recent technological advances have explored several high-throughput platforms to reveal many "unexpected" protein-small molecule interactions that could have profound impact on our understanding of cell signaling. These interactions will help bridge gaps in existing regulatory loops of cell signaling and serve as new targets for medical intervention. In this review, we summarize recent advances of systematic investigation of protein-metabolite/small molecule interactions, and discuss the impact of such studies and their potential impact on both biological researches and medicine.
细胞信号广泛存在于细胞成分之间,以维持细胞的增殖、分化和适应。这种相互作用网络通常表现为蛋白质功能如何通过与其他细胞成分(包括小分子代谢物)相互作用来调节。虽然许多生化相互作用已经被确定为蛋白质酶与其底物和产物之间的反应,但在系统水平上,小分子代谢物如何通过变构结合来调节蛋白质功能的了解要少得多。在过去的十年中,蛋白质-小分子相互作用的研究一直落后于其他类型的相互作用。最近的技术进步探索了几种高通量平台,揭示了许多“意外”的蛋白质-小分子相互作用,这可能对我们理解细胞信号有深远的影响。这些相互作用将有助于弥合细胞信号现有调节回路中的差距,并为医学干预提供新的靶点。在这篇综述中,我们总结了系统研究蛋白质-代谢物/小分子相互作用的最新进展,并讨论了这些研究的影响及其对生物学研究和医学的潜在影响。