Title The transport of alpha(1A)-adrenergic receptor with 33-nm step size in live cells
Authors Liang, Zhang-Yi
Xu, Ning
Guan, Ying-Hua
Xu, Ming
He, Qi-Hua
Han, Qi-De
Zhang, You-Yi
Zhao, Xin-Sheng
Affiliation Peking Univ, Beijing Natl Lab Mol Sci, State Key Lab Struct Chem Unstable & Stable Speci, Beijing 100871, Peoples R China.
Peking Univ, Dept Biol Chem, Coll Chem & Mol Engn, Beijing 100871, Peoples R China.
Peking Univ Third Hosp, Inst Vasc Med, Beijing 100083, Peoples R China.
Minist Educ, Key Lab Mol Cardiovasc Sci, Beijing 100083, Peoples R China.
Peking Univ, Ctr Med Anal, Hlth Sci Ctr, Beijing 100083, Peoples R China.
Keywords alpha(1A)-adrenergic receptor
transport
living cell
actin
real time
single particle tracking
myosin
PROTEIN-COUPLED RECEPTORS
HAND-OVER-HAND
MYOSIN-V
ALPHA(1)-ADRENOCEPTOR SUBTYPES
MEDIATED INTERNALIZATION
ACTIN
ALPHA(1B)-ADRENOCEPTOR
DESENSITIZATION
LOCALIZATION
MECHANISM
Issue Date 2007
Publisher 生物化学与生物物理学研究通讯
Citation BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS.2007,353,(2),231-237.
Abstract We used the technique of single particle tracking (SPT) with high tempo-spatial resolution to efficiently explore the route and mechanism for the transport Of alpha(1A)-adrenergic receptor (alpha(1A)-AR) in real time in living cells. We found that the initial transport Of alpha(1A)-AR in cells depended on actin filaments with the velocity of 0.2 mu m/s and exhibited discrete 33-nm steps. It was noted that the step size, the rate constant, and the velocities were in accordance with the character of single myosin in vitro, implying that while transporting each endosome myosins did not work in the "tug-of-war" mode and that they did not adopt the strategy to boost up transporting speed by working coordinately. These results provided insight into the mechanism of GPCR transport ill vivo. (c) 2006 Elsevier Inc. All rights reserved.
URI http://hdl.handle.net/20.500.11897/198543
ISSN 0006-291X
DOI 10.1016/j.bbrc.2006.11.116
Indexed SCI(E)
PubMed
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