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光学镊子研究 Notch:单分子相互作用强度与配体内吞无关。

Optical tweezers studies on Notch: single-molecule interaction strength is independent of ligand endocytosis.

机构信息

Department of Biomedical Engineering, UCI, Irvine, CA 92612, USA.

出版信息

Dev Cell. 2012 Jun 12;22(6):1313-20. doi: 10.1016/j.devcel.2012.04.007. Epub 2012 May 31.

Abstract

Notch signaling controls diverse cellular processes critical to development and disease. Cell surface ligands bind Notch on neighboring cells but require endocytosis to activate signaling. The role ligand endocytosis plays in Notch activation has not been established. Here we integrate optical tweezers with cell biological and biochemical methods to test the prevailing model that ligand endocytosis facilitates recycling to enhance ligand interactions with Notch necessary to trigger signaling. Specifically, single-molecule measurements indicate that interference of ligand endocytosis and/or recycling does not alter the force required to rupture bonds formed between cells expressing the Notch ligand Delta-like1 (Dll1) and laser-trapped Notch1 beads. Together, our analyses eliminate roles for ligand endocytosis and recycling in Dll1-Notch1 interactions and indicate that recycling indirectly affects signaling by regulating the accumulation of cell surface ligand. Importantly, our study demonstrates the utility of optical tweezers to test a role for ligand endocytosis in generating cell-mediated mechanical force.

摘要

Notch 信号通路控制着许多对发育和疾病至关重要的细胞过程。细胞表面配体与相邻细胞上的 Notch 结合,但需要内吞作用才能激活信号通路。配体内吞作用在 Notch 激活中的作用尚未确定。在这里,我们将光学镊子与细胞生物学和生化方法相结合,以测试目前的模型,即配体内吞作用有助于循环,从而增强与 Notch 的配体相互作用,从而触发信号转导。具体而言,单分子测量表明,干扰配体的内吞作用和/或循环不会改变在表达 Notch 配体 Delta-like1 (Dll1) 的细胞和激光捕获的 Notch1 珠之间形成的键断裂所需的力。综上所述,我们的分析排除了配体内吞作用和循环在 Dll1-Notch1 相互作用中的作用,并表明循环通过调节细胞表面配体的积累间接影响信号转导。重要的是,我们的研究证明了光学镊子在测试配体内吞作用在产生细胞介导的机械力中的作用的实用性。

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