Department of Physics, Center for the Physics of Living Cells and Institute for Genomic Biology University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.
Science. 2013 May 24;340(6135):991-4. doi: 10.1126/science.1231041.
Cell-cell and cell-matrix mechanical interactions through membrane receptors direct a wide range of cellular functions and orchestrate the development of multicellular organisms. To define the single molecular forces required to activate signaling through a ligand-receptor bond, we developed the tension gauge tether (TGT) approach in which the ligand is immobilized to a surface through a rupturable tether before receptor engagement. TGT serves as an autonomous gauge to restrict the receptor-ligand tension. Using a range of tethers with tunable tension tolerances, we show that cells apply a universal peak tension of about 40 piconewtons (pN) to single integrin-ligand bonds during initial adhesion. We find that less than 12 pN is required to activate Notch receptors. TGT can also provide a defined molecular mechanical cue to regulate cellular functions.
细胞膜受体介导的细胞-细胞和细胞-基质相互作用可以指导广泛的细胞功能,并协调多细胞生物的发育。为了定义激活配体-受体键合信号所需的单个分子力,我们开发了张力计系绳(TGT)方法,其中在受体结合之前,通过可断裂的系绳将配体固定在表面上。TGT 作为一个自主的测量仪,限制了受体-配体的张力。我们使用一系列具有可调张力容限的系绳,表明细胞在初始黏附过程中对单个整合素-配体键施加约 40 皮牛顿(pN)的通用峰值张力。我们发现,激活 Notch 受体所需的张力小于 12 pN。TGT 还可以提供定义明确的分子力学线索来调节细胞功能。