| Literature DB >> 31081612 |
Feng-Jen Hsieh1,2, Shingo Sotoma1, Hsin-Hung Lin1, Ching-Ya Cheng1, Tsyr-Yan Yu1, Chia-Lung Hsieh1, Chun-Hung Lin2, Huan-Cheng Chang1,3,4.
Abstract
Real-time tracking of membrane proteins is essential to gain an in-depth understanding of their dynamics on the cell surface. However, conventional fluorescence imaging with molecular probes like organic dyes and fluorescent proteins often suffers from photobleaching of the fluorophores, thus hindering their use for continuous long-term observations. With the availability of fluorescent nanodiamonds (FNDs), which have superb biocompatibility and excellent photostability, it is now possible to conduct the imaging in both short and long terms with high temporal and spatial resolution. To realize the concept, we have developed a facile method (e.g., one-pot preparation) to produce alkyne-functionalized hyperbranched-polyglycerol-coated FNDs for bioorthogonal labeling of azide-modified membrane proteins and azide-modified antibodies of membrane proteins. The high specificity of this labeling method has allowed us to continuously monitor the movements of the proteins of interest (such as integrin α5) on/in living cells over 2 h. The results open a new horizon for live cell imaging with functional nanoparticles and fluorescence microscopy.Entities:
Keywords: cells; fluorescence imaging; glycoproteins; membrane proteins; nanodiamonds
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Year: 2019 PMID: 31081612 DOI: 10.1021/acsami.9b03640
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229