Abstract
We investigate the mechanism of photobleaching of fluorescent proteins using nonlinear Fourier-transform spectroscopy with ultrabroadband femtosecond pulses. Photobleaching of fluorescent molecules occurs through one-photon excited-state absorption following two-photon excitation from the ground state.
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References
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Acknowledgements
We would like to thank Drs. K. Isobe, K. Midorikawa, and A. Miyawaki of RIKEN, and Prof. F. Kannari of Keio Univ. for their support and cooperation during the work. This work was supported in part by the Grants-in-Aid for Scientific Research (No. 24560052) and the Strategic Research Foundation Grant-aided Project for Private Universities, both from the MEXT, Japan.
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Suda, A., Takahashi, H., Toda, K. (2015). Nonlinear Fourier-Transform Spectroscopy Using Ultrabroadband Femtosecond Pulses for the Measurement of Photobleaching of Fluorescent Proteins. In: Yamanouchi, K., Cundiff, S., de Vivie-Riedle, R., Kuwata-Gonokami, M., DiMauro, L. (eds) Ultrafast Phenomena XIX. Springer Proceedings in Physics, vol 162. Springer, Cham. https://doi.org/10.1007/978-3-319-13242-6_133
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DOI: https://doi.org/10.1007/978-3-319-13242-6_133
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