Super-resolution imaging and tracking of TGF-β receptor II on living cells

被引:12
作者
Ye, Zi [1 ]
Li, Nan [1 ]
Zhao, Libo [1 ]
Sun, Yahong [1 ]
Ruan, Hefei [1 ]
Zhang, Mingliang [1 ]
Yuan, Jinghe [1 ]
Fang, Xiaohong [1 ]
机构
[1] Chinese Acad Sci, Beijing Natl Lab Mol Sci, Inst Chem, Key Lab Mol Nanostruct & Nanotechnol, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
Single-particle tracking; Photoactivated localization microscopy; Single-molecule fluorescence imaging; TGF-beta receptor II; Membrane diffusion; SINGLE-MOLECULE FLUORESCENCE; HUMAN PANCREATIC-CANCER; ENHANCED EXPRESSION; PARTICLE TRACKING; MEMBRANE; MICROSCOPY; DIMERIZATION; DIFFUSION; PROTEINS;
D O I
10.1007/s11434-016-1043-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Single-particle tracking photoactivated localization microscopy (sptPALM) has recently emerged as a powerful tool for high-density imaging and tracking of individual molecules in living cells. In this work, we have monitored and compared the diffusion dynamics of TGF-beta type II receptor (T beta RII) at high expression level using both traditional single-particle tracking (SPT) and sptPALM. The ligand-induced aggregation of TbRII oligomers was further indicated by sptPALM. Due to the capacity of distinguishing and tracking single molecules within diffraction limit, sptPALM outperforms traditional SPT by providing more accurate biophysical information.
引用
收藏
页码:632 / 638
页数:7
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