Polarized two-photon photoselection in EGFP: Theory and experiment
Author(s) -
Thomas A. Masters,
Richard J. Marsh,
Thomas S. Blacker,
Daven A. Armoogum,
Banafshé Larijani,
Angus J. Bain
Publication year - 2018
Publication title -
the journal of chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.071
H-Index - 357
eISSN - 1089-7690
pISSN - 0021-9606
DOI - 10.1063/1.5011642
Subject(s) - transition dipole moment , excited state , tensor (intrinsic definition) , dipole , anisotropy , magnetic dipole transition , two photon absorption , two photon excitation microscopy , physics , molecular physics , excitation , photon , absorption (acoustics) , isotropy , atomic physics , fluorescence , chemistry , optics , electric dipole transition , magnetic dipole , quantum mechanics , geometry , laser , mathematics
In this work, we present a complete theoretical description of the excited state order created by two-photon photoselection from an isotropic ground state; this encompasses both the conventionally measured quadrupolar (K = 2) and the "hidden" degree of hexadecapolar (K = 4) transition dipole alignment, their dependence on the two-photon transition tensor and emission transition dipole moment orientation. Linearly and circularly polarized two-photon absorption (TPA) and time-resolved single- and two-photon fluorescence anisotropy measurements are used to determine the structure of the transition tensor in the deprotonated form of enhanced green fluorescent protein. For excitation wavelengths between 800 nm and 900 nm, TPA is best described by a single element, almost completely diagonal, two-dimensional (planar) transition tensor whose principal axis is collinear to that of the single-photon S → S transition moment. These observations are in accordance with assignments of the near-infrared two-photon absorption band in fluorescent proteins to a vibronically enhanced S → S transition.
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