| Literature DB >> 16610918 |
Stefanie Y Nishimura1, Samuel J Lord, Lawrence O Klein, Katherine A Willets, Meng He, Zhikuan Lu, Robert J Twieg, W E Moerner.
Abstract
The dicyanomethylenedihydrofuran (DCDHF) class of single-molecule fluorophores contains an amine donor and a dicyanomethylenedihydrofuran acceptor linked by a conjugated unit (benzene, naphthalene, or styrene). Molecules in this class have a number of useful properties in addition to those usually required for single-molecule studies (such as high fluorescence quantum yield and photostability), including second-order optical nonlinearity, large ground-state dipole moment, and sensitivity to local environment. Moreover, most DCDHF molecules have amphiphilic structures, with a polar dicyanomethylenedihydrofuran headgroup and nonpolar hydrocarbon tails on the amine or furan ring, and can be used as fluorescent lipid analogues for live cell imaging. Here we demonstrate that individual molecules of several different DCDHF lipid analogues can be observed diffusing in the plasma membrane of Chinese hamster ovary cells. The photophysical and diffusive behaviors of the DCDHF lipid analogues in membranes are described and are found to be competitive with the well-known lipid probe N-(6-tetramethylrhodaminethiocarbamoyl)-1,2-dihexadecanoyl-sn-glycero-3-phosphoethanolamine.Entities:
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Year: 2006 PMID: 16610918 PMCID: PMC1702323 DOI: 10.1021/jp0574145
Source DB: PubMed Journal: J Phys Chem B ISSN: 1520-5207 Impact factor: 2.991