| Autor: |
Ropp JD; Department of Pulmonary Research, Genentech, Inc., South San Francisco, California, USA., Donahue CJ, Wolfgang-Kimball D, Hooley JJ, Chin JY, Cuthbertson RA, Bauer KD |
| Jazyk: |
angličtina |
| Zdroj: |
Cytometry [Cytometry] 1996 Jul 01; Vol. 24 (3), pp. 284-8. |
| DOI: |
10.1002/(SICI)1097-0320(19960701)24:3<284::AID-CYTO12>3.0.CO;2-M |
| Abstrakt: |
Aequorea green fluorescent protein (GFP) has been expressed in a variety of cell lines and host organisms. A recent report (Heim et al.: Proc Natl Acad Sci USA 91:12501-12504, 1994) has documented that a GFP mutant with a single amino acid substitution (tyrosine 66 to histidine; Y66H-GFP) elicits altered spectral properties. Whereas wild-type GFP emits with a maximum at approximately 509 nm (green fluorescence), Y66H-GFP fluoresces with a maximum at approximately 448 nm (blue fluorescence). In this study we employed available argon and krypton ion laser lines to investigate the impact of laser excitation wavelength on the detection of Y66H-GEP by flow cytometry. Using transiently transfected 293 cells, a cellular subpopulation with elevated blue fluorescence was detectable with excitation at 407 nm, but not with ultraviolet (UV), 458 nm, or 488 nm excitation. The blue-fluorescing cells were further documented to express Y66H-GFP by immunoblot analysis of sorted cells. Finally, we demonstrated the simultaneous analysis of both wild-type and Y66H-GFP in cotransfected 293 cells using 407 nm excitation while collecting blue fluorescence at 460 +/- 20 nm (Y66H-GFP) and green fluorescence at 525 +/- 25 nm (wild-type GFP). These studies illustrate the potential for assessing differential gene expression by simultaneously analyzing multiple GFP species with multiparameter flow cytometry. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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