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本文引用的文献

1
Defining single molecular forces required to activate integrin and notch signaling.定义激活整合素和 Notch 信号所需的单个分子力。
Science. 2013 May 24;340(6135):991-4. doi: 10.1126/science.1231041.
2
Tension sensing nanoparticles for mechano-imaging at the living/nonliving interface.用于活体/非活体界面力学成像的张力感应纳米颗粒。
J Am Chem Soc. 2013 Apr 10;135(14):5320-3. doi: 10.1021/ja401494e. Epub 2013 Mar 26.
3
Direct observation of proteolytic cleavage at the S2 site upon forced unfolding of the Notch negative regulatory region.强制展开 Notch 负调控区时 S2 位点蛋白水解切割的直接观察。
Proc Natl Acad Sci U S A. 2012 Oct 9;109(41):E2757-65. doi: 10.1073/pnas.1205788109. Epub 2012 Sep 24.
4
Notch ligand endocytosis generates mechanical pulling force dependent on dynamin, epsins, and actin.Notch 配体内吞作用产生依赖于胞质动力蛋白、衔接蛋白和肌动蛋白的机械牵拉力。
Dev Cell. 2012 Jun 12;22(6):1299-312. doi: 10.1016/j.devcel.2012.04.005. Epub 2012 May 31.
5
Optical tweezers studies on Notch: single-molecule interaction strength is independent of ligand endocytosis.光学镊子研究 Notch:单分子相互作用强度与配体内吞无关。
Dev Cell. 2012 Jun 12;22(6):1313-20. doi: 10.1016/j.devcel.2012.04.007. Epub 2012 May 31.
6
Ligand mobility modulates immunological synapse formation and T cell activation.配体流动性调节免疫突触形成和 T 细胞激活。
PLoS One. 2012;7(2):e32398. doi: 10.1371/journal.pone.0032398. Epub 2012 Feb 22.
7
Comparison of the energetics of avidin, streptavidin, neutrAvidin, and anti-biotin antibody binding to biotinylated lipid bilayer examined by second-harmonic generation.通过二次谐波产生研究生物素化脂质双层与亲和素、链霉亲和素、中性亲和素和抗生物素抗体结合的能量学比较。
Anal Chem. 2012 Jan 3;84(1):201-8. doi: 10.1021/ac202375n. Epub 2011 Dec 19.
8
Visualizing mechanical tension across membrane receptors with a fluorescent sensor.利用荧光传感器可视化跨膜受体的机械张力。
Nat Methods. 2011 Oct 30;9(1):64-7. doi: 10.1038/nmeth.1747.
9
Force-induced unfolding simulations of the human Notch1 negative regulatory region: possible roles of the heterodimerization domain in mechanosensing.力诱导的人 Notch1 负调控区的展开模拟:异二聚化结构域在机械感知中的可能作用。
PLoS One. 2011;6(7):e22837. doi: 10.1371/journal.pone.0022837. Epub 2011 Jul 28.
10
Evidence for increased exposure of the Notch1 metalloprotease cleavage site upon conversion to an activated conformation.证据表明 Notch1 金属蛋白酶裂解位点在转化为激活构象时暴露增加。
Structure. 2011 Apr 13;19(4):546-54. doi: 10.1016/j.str.2011.01.016.

膜结合的 Delta 激活 Notch,并揭示了信号通路的空间 - 机械调节的作用。

Membrane tethered delta activates notch and reveals a role for spatio-mechanical regulation of the signaling pathway.

机构信息

Department of Chemistry, Emory University, Atlanta, Georgia.

Department of Chemistry, Emory University, Atlanta, Georgia.

出版信息

Biophys J. 2013 Dec 17;105(12):2655-65. doi: 10.1016/j.bpj.2013.11.012.

DOI:10.1016/j.bpj.2013.11.012
PMID:24359737
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3882513/
Abstract

Short-range Notch receptor signaling is necessary for coordinating developmental activities in metazoa. To investigate this juxtacrine pathway, we mimic receptor-ligand binding within the cell-cell junction by engaging Notch1-eGFP expressing cells to a supported lipid membrane displaying Delta-like protein 4 (DLL4). DLL4-Notch1 binding, oligomerization, and transport were observed in real time, and the molecular density and stoichiometry of the complexes were determined using quantitative fluorescence imaging. A Notch transcriptional reporter readout was used to quantify how ligand lateral mobility, orientation, and density modulate receptor activation levels. These experiments demonstrate that limiting the lateral mobility of DLL4 can enhance Notch activation by 2.6-fold, thus supporting the existence of a spatio-mechanical mechanism of signal regulation.

摘要

短程 Notch 受体信号对于协调后生动物的发育活动是必要的。为了研究这种旁分泌途径,我们通过将 Notch1-eGFP 表达细胞与展示 Delta-like protein 4 (DLL4) 的支持脂质膜结合,模拟细胞-细胞连接内的受体-配体结合。实时观察 DLL4-Notch1 结合、寡聚化和运输,并用定量荧光成像确定复合物的分子密度和化学计量。使用 Notch 转录报告基因读数来量化配体横向流动性、方向和密度如何调节受体激活水平。这些实验表明,限制 DLL4 的横向流动性可以将 Notch 激活提高 2.6 倍,从而支持信号调节的空间机械机制的存在。