You Mingxu, Lyu Yifan, Han Da, Qiu Liping, Liu Qiaoling, Chen Tao, Sam Wu Cuichen, Peng Lu, Zhang Liqin, Bao Gang, Tan Weihong
Molecular Science and Biomedicine Laboratory, State Key Laboratory of Chemo/Bio-sensing and Chemometrics, College of Chemistry and Chemical Engineering, College of Biology, Collaborative Innovation Center for Chemistry and Molecular Medicine, Hunan University, Changsha 410082, People's Republic of China.
Department of Chemistry and Department of Physiology and Functional Genomics, Center for Research at the Bio/Nano Interface, Health Cancer Center, UF Genetics Institute, McKnight Brain Institute, University of Florida, Gainesville, Florida 32611, USA.
Nat Nanotechnol. 2017 May;12(5):453-459. doi: 10.1038/nnano.2017.23. Epub 2017 Mar 20.
Cells interact with the extracellular environment through molecules expressed on the membrane. Disruption of these membrane-bound interactions (or encounters) can result in disease progression. Advances in super-resolution microscopy have allowed membrane encounters to be examined, however, these methods cannot image entire membranes and cannot provide information on the dynamic interactions between membrane-bound molecules. Here, we show a novel DNA probe that can transduce transient membrane encounter events into readable cumulative fluorescence signals. The probe, which translocates from one anchor site to another, mimicking motor proteins, is realized through a toehold-mediated DNA strand displacement reaction. Using this probe, we successfully monitored rapid encounter events of membrane lipid domains using flow cytometry and fluorescence microscopy. Our results show a preference for encounters within the same lipid domains.
细胞通过膜上表达的分子与细胞外环境相互作用。这些膜结合相互作用(或相遇)的破坏会导致疾病进展。超分辨率显微镜技术的进步使得膜相遇得以研究,然而,这些方法无法对整个膜进行成像,也无法提供关于膜结合分子之间动态相互作用的信息。在此,我们展示了一种新型DNA探针,它可以将瞬时膜相遇事件转化为可读的累积荧光信号。该探针从一个锚定位点转移到另一个锚定位点,模仿驱动蛋白,通过一种由链置换引发的DNA链置换反应实现。使用该探针,我们通过流式细胞术和荧光显微镜成功监测了膜脂域的快速相遇事件。我们的结果表明,同一脂域内的相遇更受青睐。