| Title | Dynamic behaviors of a1B-adrenergic receptor in living cells |
| Authors | Xu, Ming Guan, Ying-Hua Xu, Ning Liang, Zhang-Yi Lu, Zhi-Zhen Han, Qi-De Zhao, Xin-Sheng Zhang, You-Yi |
| Affiliation | Key Laboratory of Molecular Cardiovascular Sciences, Peking University Third Hospital, Ministry of Education, Beijing 100083, China Department of Chemical Biology, College of Chemistry, Peking University, Beijing 100871, China |
| Issue Date | 2007 |
| Citation | China International Conference on Nanoscience and Technology, ChinaNANO 2005.Beijing, China,121-123(771-776). |
| Abstract | AIM: The present study aims at investigating dynamic behaviors of a 1B-adrenergic receptor (a1B-AR) at molecular level in living cells. METHODS: Wide-field imaging was applied on the detection of real-time dynamic behaviors of a1B-AR using fluorescence-labeled prazosin (Praz), a specific antagonist of ??1-AR, in a 1B-AR stably expressed human embryonic kidney 293 (HEK293) living cells. The precise localization around 10 nanometers with 2D Gaussian function was applied in the analysis of the trajectory of molecular movement. RESULTS: The specific binding characteristic of BODIPY-Praz in living cells was identified by the real-time observation that phentolamine competitively inhibits the BODIPY-Praz binding to the receptor at a molecular level in HEK293 living cell. The directional and trapped motions of a1B-AR molecules in living cells were observed and analyzed at millisecond time resolution and nanometer space resolution. The speeds of the two typical motions were distributed in two different scopes with the peak value of 1.08 and 0.55 ??m/s, respectively. The directed motions in living cells were obviously diminished by the previous incubation with the microtubule disrupting agent nocodazole. CONCLUSION: a1B-AR with binding function was visualized by BODIPY-labeled Praz at molecular level in living cells. The directed and trapped motions have the different speed distributions in living cells. The directed motion of a1B-AR in living cells might be 'walking' along microtubules. |
| URI | http://hdl.handle.net/20.500.11897/310624 |
| ISSN | 9783908451303 |
| Indexed | EI |
| Appears in Collections: | 第三医院 å å¦ä¸ å å å·¥ç¨ å¦é ¢ |
