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使用基于DNA的荧光探针量化细胞间连接的拉力。

Quantifying tensile forces at cell-cell junctions with a DNA-based fluorescent probe.

作者信息

Zhao Bin, Li Ningwei, Xie Tianfa, Bagheri Yousef, Liang Chungwen, Keshri Puspam, Sun Yubing, You Mingxu

机构信息

Department of Chemistry, University of Massachusetts Amherst Massachusetts 01003 USA

Department of Mechanical & Industrial Engineering, University of Massachusetts Amherst Massachusetts 01003 USA

出版信息

Chem Sci. 2020 Jul 29;11(32):8558-8566. doi: 10.1039/d0sc01455a.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1512/8163409/57a1f412db52/d0sc01455a-f1.jpg

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