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J Phys Chem B. 2014 Dec 18;118(50):14627-31. doi: 10.1021/jp511126x. Epub 2014 Dec 8.

Application of three-photon excitation FCS to the study of protein oligomerization.

Author information

1
Laboratory for Fluorescence Dynamics, Biomedical Engineering, University of California, Irvine , Irvine, California 92697, United States.

Abstract

Three-photon excitation fluorescence correlation spectroscopy was used to detect oligomerization equilibria of rat liver phosphofructokinase. The fluorescence intensity produced by the three-photon excitation of tryptophan was collected using the DIVER microscope. In this home-built upright microscope, a large area photomultiplier, placed directly below the sample, is used as the detector. The lack of optical elements in the microscope detection path results in a significantly improved detection efficiency in the UV region down to about 300 nm, which encompasses the fluorescence emission from tryptophan. The three-photon excitation autocorrelation decays obtained for phosphofructokinase in the presence of F6P showed the presence of large oligomers. Substitution of F6P with ATP in the buffer medium results in dissociation of the large oligomers, which is reported by the decreased autocorrelation amplitude. The three-photon excitation process was verified from the slope of the log-log plot of intensity against laser power.

PMID:
25438088
PMCID:
PMC4275161
DOI:
10.1021/jp511126x
[Indexed for MEDLINE]
Free PMC Article

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