Vilardaga Jean-Pierre, Bünemann Moritz, Krasel Cornelius, Castro Mariàn, Lohse Martin J
Institute of Pharmacology and Toxicology, University of Würzburg, Versbacher Str. 9, D-97078 Würzburg, Germany.
Nat Biotechnol. 2003 Jul;21(7):807-12. doi: 10.1038/nbt838. Epub 2003 Jun 15.
Hormones and neurotransmitters transduce signals through G protein-coupled receptors (GPCR). Despite their common signaling pathways, however, the responses they elicit have different temporal patterns. To reveal the molecular basis for these differences we have developed a generally applicable fluorescence-based technique for real-time monitoring of the activation switch of GPCRs in living cells. We used such direct measurements to investigate the activation of the alpha(2A)-adrenergic receptor (alpha(2A)AR; neurotransmitter) and the parathyroid hormone receptor (PTHR; hormone) and observed much faster kinetics than expected: approximately 40 ms for the alpha(2A)AR and approximately 1 s for the PTHR. The different switch times are in agreement with the different receptors' biological functions. Agonists and antagonists could rapidly switch the receptors on or off, whereas a partial agonist caused only a partial signal. This approach allows the comparison of agonist and partial agonist intrinsic activities at the receptor level and provides evidence for millisecond activation times of GPCRs.
激素和神经递质通过G蛋白偶联受体(GPCR)转导信号。然而,尽管它们具有共同的信号通路,但它们引发的反应却具有不同的时间模式。为了揭示这些差异的分子基础,我们开发了一种普遍适用的基于荧光的技术,用于实时监测活细胞中GPCR激活开关。我们使用这种直接测量方法来研究α(2A)-肾上腺素能受体(α(2A)AR;神经递质)和甲状旁腺激素受体(PTHR;激素)的激活,并观察到比预期快得多的动力学:α(2A)AR约为40毫秒,PTHR约为1秒。不同的开关时间与不同受体的生物学功能一致。激动剂和拮抗剂可以迅速打开或关闭受体,而部分激动剂仅引起部分信号。这种方法允许在受体水平上比较激动剂和部分激动剂的内在活性,并为GPCR的毫秒级激活时间提供证据。