Rudolf Virchow Center for Integrative and Translational Bioimaging, University of Würzburg, Josef-Schneider-Str. 2, 97080, Würzburg, Germany.
Department of Biotechnology and Biophysics, Biocenter, University of Würzburg, Am Hubland, 97074, Würzburg, Germany.
Commun Biol. 2022 Feb 28;5(1):176. doi: 10.1038/s42003-022-03106-4.
G-protein-coupled receptors (GPCRs) are hypothesized to possess molecular mobility over a wide temporal range. Until now the temporal range has not been fully accessible due to the crucially limited temporal range of available methods. This in turn, may lead relevant dynamic constants to remain masked. Here, we expand this dynamic range by combining fluorescent techniques using a spot confocal setup. We decipher mobility constants of β-adrenergic receptor over a wide time range (nanosecond to second). Particularly, a translational mobility (10 µm²/s), one order of magnitude faster than membrane associated lateral mobility that explains membrane protein turnover and suggests a wider picture of the GPCR availability on the plasma membrane. And a so far elusive rotational mobility (1-200 µs) which depicts a previously overlooked dynamic component that, despite all complexity, behaves largely as predicted by the Saffman-Delbrück model.
G 蛋白偶联受体(GPCRs)被假设具有广泛的时间范围内的分子流动性。到目前为止,由于可用方法的时间范围受到严格限制,这个时间范围还没有完全能够被获取到。这反过来可能导致相关的动态常数仍然被掩盖。在这里,我们通过结合使用点共焦设置的荧光技术来扩展这个动态范围。我们在广泛的时间范围内(纳秒到秒)解析了β-肾上腺素能受体的流动性常数。特别是,一种平移流动性(10µm²/s),比膜相关的侧向流动性快一个数量级,这解释了膜蛋白周转,并表明了 GPCR 在质膜上的可用性的更广泛的情况。还有一个目前难以捉摸的旋转流动性(1-200µs),它描绘了一个以前被忽视的动态组成部分,尽管存在所有的复杂性,但它的行为在很大程度上符合 Saffman-Delbrück 模型的预测。