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| Content Provider | Royal Society of Chemistry (RSC) |
|---|---|
| Author | Ha, Hyung-Ho Chang, Young-Tae Son, Jyunghyun Lee, Jae-Jung |
| Copyright Year | 2011 |
| Abstract | Imaging a specific protein of interest in live cell has versatile applications in biological research. Recently, diverse chemical tags have been developed to overcome the limits of autofluorescence protein (FP) tags. However, current chemical methods still need to be progressed to compete with FPs in the scope of specificity and convenience in staining procedure. We report a novel protein tagging method that provides a convenient and specific fluorescent labeling of membrane proteins. Ω tag is developed by employing a mammalian enzymeglutathione sulfur-transferase omega 1 (GSTO1) and its partner dye, 5-bromomethyl fluorescein (BMF). Ω-tagged membrane proteins were labeled by BMF efficiently for live cell imaging and in-gel analysis. Endocytosis of epidermal growth factor receptor (EGFR) was successfully visualized by using this Ω tagging system. Ω tag will provide a convenient tool for the physiological study of membrane proteins in live cells. |
| Starting Page | 1270 |
| Ending Page | 1276 |
| Page Count | 7 |
| File Format | HTM / HTML PDF |
| ISSN | 1742206X |
| Volume Number | 7 |
| Issue Number | 4 |
| Journal | Molecular BioSystems |
| DOI | 10.1039/c0mb00327a |
| Language | English |
| Publisher | Royal Society of Chemistry |
| Access Restriction | Open |
| Subject Keyword | Endocytosis GSTO1 Cell surface receptor Autofluorescence Fluorescein Staining EGFR Protein Epidermal growth factor receptor Growth factor |
| Content Type | Text |
| Resource Type | Article |
| Subject | Molecular Biology Biotechnology |
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