Zhao Bin, Li Ningwei, Xie Tianfa, Bagheri Yousef, Liang Chungwen, Keshri Puspam, Sun Yubing, You Mingxu
Department of Chemistry, University of Massachusetts Amherst Massachusetts 01003 USA
Department of Mechanical & Industrial Engineering, University of Massachusetts Amherst Massachusetts 01003 USA
Chem Sci. 2020 Jul 29;11(32):8558-8566. doi: 10.1039/d0sc01455a.
Cells are physically contacting with each other. Direct and precise quantification of forces at cell-cell junctions is still challenging. Herein, we have developed a DNA-based ratiometric fluorescent probe, termed DNAMeter, to quantify intercellular tensile forces. These lipid-modified DNAMeters can spontaneously anchor onto live cell membranes. The DNAMeter consists of two self-assembled DNA hairpins of different force tolerance. Once the intercellular tension exceeds the force tolerance to unfold a DNA hairpin, a specific fluorescence signal will be activated, which enables the real-time imaging and quantification of tensile forces. Using E-cadherin-modified DNAMeter as an example, we have demonstrated an approach to quantify, at the molecular level, the magnitude and distribution of E-cadherin tension among epithelial cells. Compatible with readily accessible fluorescence microscopes, these easy-to-use DNA tension probes can be broadly used to quantify mechanotransduction in collective cell behaviors.
细胞之间存在物理接触。对细胞间连接处以力进行直接且精确的量化仍然具有挑战性。在此,我们开发了一种基于DNA的比率荧光探针,称为DNAMeter,用于量化细胞间拉力。这些脂质修饰的DNAMeter能够自发地锚定在活细胞膜上。DNAMeter由两个具有不同力耐受性的自组装DNA发夹组成。一旦细胞间张力超过使DNA发夹展开的力耐受性,就会激活特定的荧光信号,从而实现对拉力的实时成像和量化。以E-钙粘蛋白修饰的DNAMeter为例,我们展示了一种在分子水平上量化上皮细胞中E-钙粘蛋白张力大小和分布的方法。这些易于使用的DNA张力探针与易于获得的荧光显微镜兼容,可广泛用于量化集体细胞行为中的机械转导。