Department of Chemistry, Emory University, Atlanta, GA 30322, USA.
Angew Chem Int Ed Engl. 2023 Jul 24;62(30):e202302967. doi: 10.1002/anie.202302967. Epub 2023 May 15.
Immune recognition occurs at specialized cell-cell junctions when immune cells and target cells physically touch. In this junction, groups of receptor-ligand complexes assemble and experience molecular forces that are ultimately generated by the cellular cytoskeleton. These forces are in the range of piconewton (pN) but play crucial roles in immune cell activation and subsequent effector responses. In this minireview, we will review the development of DNA based molecular tension sensors and their applications in mapping and quantifying mechanical forces experienced by immunoreceptors including T-cell receptor (TCR), Lymphocyte function-associated antigen (LFA-1), and the B-cell receptor (BCR) among others. In addition, we will highlight the use of DNA as a mechanical gate to manipulate mechanotransduction and decipher how mechanical forces regulate antigen discrimination and receptor signaling.
免疫识别发生在免疫细胞和靶细胞物理接触的特化细胞-细胞连接处。在这个连接处,受体-配体复合物聚集,并经历由细胞细胞骨架产生的分子力。这些力在皮牛顿(pN)范围内,但在免疫细胞激活和随后的效应子反应中起着至关重要的作用。在这篇综述中,我们将回顾基于 DNA 的分子张力传感器的发展及其在绘制和量化免疫受体(包括 T 细胞受体(TCR)、淋巴细胞功能相关抗原(LFA-1)和 B 细胞受体(BCR)等)所经历的机械力方面的应用。此外,我们将强调 DNA 作为机械门的用途,以操纵力学转导,并阐明机械力如何调节抗原识别和受体信号。