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作 者:Wei Zhang Jinghe Yuan Yong Yang Li Xu Qiang Wang Wei Zuo Xiaohong Fang Ye-Guang Chen
机构地区:[1]Beifing National Laboratory for Molecular Sciences, Institute of Chemistry, Key Laboratory of Molecular Nanostructures and Nanotechnology, Chinese Academy of Sciences, Beijing 100190, China [2]State Key Laboratory of Biomembrane and Membrane Biotechnology, School of Life Sciences, Tsinghua University, Beijing 100084, China
出 处:《Cell Research》2010年第11期1216-1223,共8页细胞研究(英文版)
基 金:This work was supported by the National Natural Science Foundation of China (90713024, 20821003, 30921004), the National Basic Research Program of China (2007CB935601, 2010CB833706) and the Chinese Academy of Sciences.
摘 要:Transforming growth factor-β (TGF-β) binds with two transmembrane serine/threonine kinase receptors, type Ⅱ (TβRII) and type Ⅰ receptors (TβRⅠ), and one accessory receptor, type Ⅲ receptor (TβRⅢ), to transduce signals across cell membranes. Previous biochemical studies suggested that TβRI and TβRIII are preexisted homo-dimers. Using single-molecule microscopy to image green fluorescent protein-labeled membrane proteins, for the first time we have demonstrated that TβRI and TβRⅢ could exist as monomers at a low expression level. Upon TGF-β1 stimu- lation, TβRI follows the general ligand-induced receptor dimerization model for activation, but this process is TβRⅡ- dependent. The monomeric status of the non-kinase receptor TβRⅢ is unchanged in the presence of TGF-β1. With the increase of receptor expression, both TβRI and TβRIII can be assembled into dimers on cell surfaces.
关 键 词:single-molecule fluorescence TGF-β signaling Type I TGF-β receptor Type Ⅲ TGF-β receptor subunit stoi-chiometry
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