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通过荧光足迹法对快速分子粘附进行定量分析。

Quantification of fast molecular adhesion by fluorescence footprinting.

作者信息

Yasunaga Adam B, Li Isaac T S

机构信息

Department of Chemistry, Biochemistry and Molecular Biology, The University of British Columbia Okanagan, Kelowna, BC, Canada.

出版信息

Sci Adv. 2021 Aug 18;7(34). doi: 10.1126/sciadv.abe6984. Print 2021 Aug.

Abstract

Rolling adhesion is a unique process in which the adhesion events are short-lived and operate under highly nonequilibrium conditions. These characteristics pose a challenge in molecular force quantification, where in situ measurement of these forces cannot be achieved with molecular force sensors that probe near equilibrium. Here, we demonstrated a quantitative adhesion footprint assay combining DNA-based nonequilibrium force probes and modeling to measure the molecular force involved in fast rolling adhesion. We were able to directly profile the ensemble molecular force distribution in our system during rolling adhesion with a dynamic range between 0 and 18 pN. Our results showed that the shear stress driving bead rolling motility directly controls the molecular tension on the probe-conjugated adhesion complex. Furthermore, the shear stress can steer the dissociation bias of components within the molecular force probe complex, favoring either DNA probe dissociation or receptor-ligand dissociation.

摘要

滚动黏附是一个独特的过程,其中黏附事件持续时间短且在高度非平衡条件下发生。这些特性给分子力定量带来了挑战,在这种情况下,使用探测接近平衡状态的分子力传感器无法实现这些力的原位测量。在这里,我们展示了一种定量黏附足迹测定法,该方法结合基于DNA的非平衡力探针和建模来测量快速滚动黏附中涉及的分子力。我们能够在滚动黏附过程中直接描绘我们系统中的整体分子力分布,动态范围为0至18皮牛。我们的结果表明,驱动珠子滚动运动的剪应力直接控制探针共轭黏附复合物上的分子张力。此外,剪应力可以引导分子力探针复合物内各组分的解离偏向,有利于DNA探针解离或受体-配体解离。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9062/8373131/f0cc4fe27916/abe6984-F1.jpg

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