Department of Life Sciences, Pohang University of Science and Technology, Pohang, Republic of Korea.
Department of Physics, Pohang University of Science and Technology, Pohang, Republic of Korea.
Exp Mol Med. 2021 Feb;53(2):291-299. doi: 10.1038/s12276-021-00567-1. Epub 2021 Feb 19.
Various repertoires of membrane protein interactions determine cellular responses to diverse environments around cells dynamically in space and time. Current assays, however, have limitations in unraveling these interactions in the physiological states in a living cell due to the lack of capability to probe the transient nature of these interactions on the crowded membrane. Here, we present a simple and robust assay that enables the investigation of transient protein interactions in living cells by using the single-molecule diffusional mobility shift assay (smDIMSA). Utilizing smDIMSA, we uncovered the interaction profile of EGFR with various membrane proteins and demonstrated the promiscuity of these interactions depending on the cancer cell line. The transient interaction profile obtained by smDIMSA will provide critical information to comprehend the crosstalk among various receptors on the plasma membrane.
各种膜蛋白相互作用的组合在细胞周围的动态时空环境中决定了细胞的反应。然而,由于缺乏探测这些相互作用在活细胞中生理状态下瞬态特性的能力,当前的测定方法在揭示这些相互作用方面存在局限性。在这里,我们提出了一种简单而强大的测定方法,通过使用单分子扩散迁移率变化分析(smDIMSA)来研究活细胞中瞬时蛋白质相互作用。利用 smDIMSA,我们揭示了 EGFR 与各种膜蛋白的相互作用模式,并证明了这些相互作用的混杂性取决于癌细胞系。通过 smDIMSA 获得的瞬时相互作用谱将为理解质膜上各种受体之间的串扰提供关键信息。