Optically Modulatable Blue Fluorescent Proteins
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- 作者：Amy E. Jablonski ; Russell B. Vegh ; Jung-Cheng Hsiang ; Bettina Bommarius ; Yen-Cheng Chen ; Kyril M. Solntsev ; Andreas S. Bommarius ; Laren M. Tolbert ; Robert M. Dickson
- 刊名：Journal of the American Chemical Society
- 出版年：2013
- 出版时间：November 6, 2013
- 年：2013
- 卷：135
- 期：44
- 页码：16410-16417
- 全文大小：345K
- 年卷期：v.135,no.44(November 6, 2013)
- ISSN：1520-5126
文摘
Blue fluorescent proteins (BFPs) offer visualization of protein location and behavior, but often suffer from high autofluorescent background and poor signal discrimination. Through dual-laser excitation of bright and photoinduced dark states, mutations to the residues surrounding the BFP chromophore enable long-wavelength optical modulation of BFP emission. Such dark state engineering enables violet-excited blue emission to be increased upon lower energy, green coillumination. Turning this green coillumination on and off at a specific frequency dynamically modulates collected blue fluorescence without generating additional background. Interpreted as transient photoconversion between neutral cis and anionic trans chromophoric forms, mutations tune photoisomerization and ground state tautomerizations to enable long-wavelength depopulation of the millisecond-lived, spectrally shifted dark states. Single mutations to the tyrosine-based blue fluorescent protein T203V/S205V exhibit enhanced modulation depth and varied frequency. Importantly, analogous single point mutations in the nonmodulatable BFP, mKalama1, creates a modulatable variant. Building modulatable BFPs offers opportunities for improved BFP signal discrimination vs background, greatly enhancing their utility.