Department of Pharmacology and Cancer Biology, Duke University, Durham, NC.
J Cardiovasc Pharmacol. 2022 Sep 1;80(3):342-353. doi: 10.1097/FJC.0000000000001185.
Understanding the activation of G protein-coupled receptors (GPCRs) is of paramount importance to the field of cardiovascular medicine due to the critical physiological roles of these receptors and their prominence as drug targets. Although many cardiovascular GPCRs have been extensively studied as model receptors for decades, new complexities in their regulation continue to emerge. As a result, there is an ongoing need to develop novel approaches to monitor and to modulate GPCR activation. In less than a decade, nanobodies, or recombinant single-domain antibody fragments from camelids, have become indispensable tools for interrogating GPCRs both in purified systems and in living cells. Nanobodies have gained traction rapidly due to their biochemical tractability and their ability to recognize defined states of native proteins. Here, we review how nanobodies have been adopted to elucidate the structure, pharmacology, and signaling of cardiovascular GPCRs, resolving long-standing mysteries and revealing unexpected mechanisms. We also discuss how advancing technologies to discover nanobodies with tailored specificities may expand the impact of these tools for both basic science and therapeutic applications.
理解 G 蛋白偶联受体 (GPCR) 的激活对于心血管医学领域至关重要,因为这些受体具有重要的生理作用,并且是药物靶点的重要选择。尽管许多心血管 GPCR 作为模型受体已经被广泛研究了几十年,但它们的调节仍然不断出现新的复杂性。因此,需要不断开发新的方法来监测和调节 GPCR 的激活。在不到十年的时间里,纳米抗体(骆驼科的重组单域抗体片段)已经成为在纯化系统和活细胞中研究 GPCR 的不可或缺的工具。由于其生化可操作性和识别天然蛋白质特定状态的能力,纳米抗体迅速得到应用。在这里,我们回顾了纳米抗体如何被用于阐明心血管 GPCR 的结构、药理学和信号转导,解决了长期存在的谜团,并揭示了意想不到的机制。我们还讨论了如何利用先进的技术发现具有定制特异性的纳米抗体,以扩大这些工具在基础科学和治疗应用中的影响力。