DNA-based ForceChrono probes for deciphering single-molecule force dynamics in living cells

被引:11
|
作者
Hu, Yuru [1 ]
Li, Hongyun [1 ]
Zhang, Chen [1 ]
Feng, Jingjing [1 ]
Wang, Wenxu [1 ]
Chen, Wei [1 ]
Yu, Miao [1 ]
Liu, Xinping [1 ]
Zhang, Xinghua [1 ]
Liu, Zheng [1 ]
机构
[1] Wuhan Univ, Inst Adv Studies, TaiKang Ctr Life & Med Sci, Hubei Key Lab Cell Homeostasis,Coll Life Sci, Wuhan 430072, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
CATCH BONDS; INTEGRIN;
D O I
10.1016/j.cell.2024.05.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Understanding cellular force transmission dynamics is crucial in mechanobiology. We developed the DNA-based ForceChrono probe to measure force magnitude, duration, and loading rates at the single- molecule level within living cells. The ForceChrono probe circumvents the limitations of in vitro single- molecule force spectroscopy by enabling direct measurements within the dynamic cellular environment. Our findings reveal integrin force loading rates of 0.5-2 pN/s and durations ranging from tens of seconds in nascent adhesions to approximately 100 s in mature focal adhesions. The probe's robust and reversible design allows for continuous monitoring of these dynamic changes as cells undergo morphological transformations. Additionally, by analyzing how mutations, deletions, or pharmacological interventions affect these parameters, we can deduce the functional roles of specific proteins or domains in cellular mechanotransduction. The ForceChrono probe provides detailed insights into the dynamics of mechanical forces, advancing our understanding of cellular mechanics and the molecular mechanisms of mechanotransduction.
引用
收藏
页码:3445 / 3459.e15
页数:31
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