Shpakov A O
Zh Evol Biokhim Fiziol. 2013 Sep-Oct;49(5):323-32.
The Nobel Prize for Chemistry in 2012 was awarded to Robert Lefkowitz and Bryan Kobilka "for studies in G-protein-coupled receptors" (GPCR). In this review the most important discoveries of these Nobel Prize winners dealing with investigation of the structure and functions of GPCR were discussed and analyzed. In the 1980s, they were the first in the world to clone GPCR--the 32-adrenergic receptor. After 20 years, the team led by B. Kobilka for the first time prepared this receptor in the crystalline form and established its three-dimensional structure. In these studies, unique approaches for purification and crystallization of other receptors were developed. In 1980s, R. Lefkowitz and his colleagues discovered beta-arrestins that regulate signal transduction occurring via GPCR. Later they revealed that beta-arrestins were the most important members of signal transduction and were responsible for the signal transduction from the hormone-activated receptor to intracellular signaling cascades independently of heterotrimeric G-proteins. These and other outstanding discoveries of R. Lefkowitz and B. Kobilka have become the basis for the novel area of molecular biology and pharmacology--the molecular endocrinology of GPCR.
2012年诺贝尔化学奖授予罗伯特·莱夫科维茨和布莱恩·科比尔卡,“以表彰他们在G蛋白偶联受体(GPCR)方面的研究”。在这篇综述中,对这些诺贝尔奖得主在GPCR结构和功能研究方面的最重要发现进行了讨论和分析。在20世纪80年代,他们是世界上首个克隆GPCR——β2肾上腺素能受体的人。20年后,由B. 科比尔卡带领的团队首次制备出这种受体的晶体形式并确定了其三维结构。在这些研究中,还开发出了用于其他受体纯化和结晶的独特方法。20世纪80年代,R. 莱夫科维茨及其同事发现了β抑制蛋白,它可调节通过GPCR发生的信号转导。后来他们揭示,β抑制蛋白是信号转导的最重要成员,负责将激素激活的受体发出的信号独立于异源三聚体G蛋白传递至细胞内信号级联反应。R. 莱夫科维茨和B. 科比尔卡的这些以及其他杰出发现,已成为分子生物学和药理学新领域——GPCR分子内分泌学的基础。