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作 者:黄超 郁苗[1] 汪文敏 廖榕玉 徐俐[1] 周林康[1] HUANG Chao,YU Miao,WANG Wen-min,LIAO Rong-yu,XU Li,ZHOU Lin-kang(School of Life Sciences, Tsinghua University, Beijing, 100084, Chin)
出 处:《现代生物医学进展》2018年第4期601-605,共5页Progress in Modern Biomedicine
基 金:中国博士后科学基金项目(2013T60103;2012M520249);周林康博士受中国科协2016-2018年度青年人才托举计划的支持
摘 要:目的:Fsp27已经被证明定位在脂滴上并且介导脂滴融合与增大。为研究Fsp27介导脂滴融合的动态分子机制,我们构建了Fsp27-mMaple3和Fsp27-mEos3.2两种新型荧光探针的融合蛋白并研究其对脂滴融合的功能影响,进而为研发Fsp27相关生理功能的光学显像技术奠定基础。方法:对照传统绿色荧光的融合蛋白Fsp27-EGFP,在共聚焦显微镜下观察Fsp27-mMaple3和Fsp27-mEos3.2两种新型融合蛋白的亚细胞定位和介导脂滴融合的功能,并利用荧光漂白恢复术(fluorescence recovery after photo-bleaching,FRAP)以判断脂滴与脂滴之间是否存在脂的交换。结果:表达Fsp27-mMaple3和Fsp27-mEos3.2两种新型融合蛋白的细胞中脂滴显著增大;同时,融合蛋白皆集中在脂滴与脂滴的接触位点上,且中性脂的交换实验显示脂滴与脂滴之间可以相互连通。结论:我们建构的两种新型荧光探针融合蛋白Fsp27-mMaple3和Fsp27-mEos3.2保持了Fsp27介导脂滴融合的功能,并为我们进一步研发新型的超分辨光学显像技术提供功能基础。Objective: Fsp27 has been proved to be localized on lipid droplets(LDs) and mediates LD growth. To study the molecular mechanism of Fsp27-mediated LD fusion, here, we investigated the functional effect of two novel fluorescent probes,Fsp27-mMaple3 and Fsp27-mEos3.2, on LD fusion for the super-resolution imaging in physiological studies. Methods: In comparison with arecently used fluorescence fused-protein Fsp27-EGFP, we observed the subcellular localization of the two novel probes and the sizes of LDs under confocal microscopy; And, fluorescence recovery after photo-bleaching(FRAP) was used to examine the lipid exchange between lipid droplets. Results: LDs expressing Fsp27-mMaple3 and Fsp27-mEos3.2 in 3T3-L1 pre-adipocytes were significantly larger than that without expression of the two probes. The FRAP experiment confirmed the normal exchange between LDs expressing the two probes. Conclusions: The two probes we constructed exhibit their comparable abilities with wild type Fsp27 in LD fusion and growth, and the study provides a functional basis on development of super-resolution imaging.
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