College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, P. R. China.
State Key Laboratory of Medicinal Chemical Biology, Tianjin Key Laboratory of Biosensing and Molecular Recognition, Research Center for Analytical Sciences, College of Chemistry, and School of Medicine, Nankai University, Tianjin 300071, P. R. China.
Anal Chem. 2022 May 31;94(21):7567-7575. doi: 10.1021/acs.analchem.2c00411. Epub 2022 May 17.
Mammalian cell display technology uses eukaryotic protein expression system to display proteins on cell surfaces and has become an important method in biological research. Although mammalian cell display technology has many advantages and development potential, certain attributes of the displayed protein remain uncharacterized, such as whether the displayed proteins re-enter the cell and how displayed proteins move into the cell. Here, we present the endocytosis mechanism, motility behavior, and transport kinetics of displayed proteins determined using HaloTag as the displayed protein and quantum dot-based single-particle tracking. The displayed protein enters the cell through clathrin-mediated endocytosis and is transported through the cell in three stages, which is dependent on microfilaments and microtubules. The dynamic information obtained in this study provides answers to questions about endocytosis and postendocytosis transport of displayed proteins and, therefore, is expected to facilitate the development of surface display technology.
哺乳动物细胞展示技术利用真核蛋白表达系统将蛋白质展示在细胞表面,已成为生物研究中的重要方法。尽管哺乳动物细胞展示技术具有许多优势和发展潜力,但展示蛋白的某些特性仍未被阐明,例如展示蛋白是否重新进入细胞以及展示蛋白如何进入细胞。在这里,我们使用 HaloTag 作为展示蛋白和基于量子点的单粒子跟踪技术,介绍了内化机制、运动行为和运输动力学。展示蛋白通过网格蛋白介导的内吞作用进入细胞,并通过三个阶段在细胞内运输,这依赖于微丝和微管。本研究获得的动态信息解答了关于展示蛋白内化和胞内运输的问题,因此有望促进表面展示技术的发展。