Fluorescence anisotropy imaging reveals localization of meso-tetrahydroxyphenyl chlorin in the nuclear envelope

被引:24
作者
Foster, TH
Pearson, BD
Mitra, S
Bigelow, CE
机构
[1] Univ Rochester, Dept Imaging Sci, Rochester, NY 14642 USA
[2] Univ Rochester, Dept Phys & Astron, Rochester, NY 14642 USA
[3] Univ Rochester, Inst Opt, Rochester, NY 14642 USA
关键词
D O I
10.1562/2005-08-11-RN-646
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have measured the intrinsic fluorescence anisotropies of six photosensitizers in homogeneous solution, and we have imaged the anisotropies of these sensitizers in tumor cell monolayers using polarization-sensitive laser-scanning confocal microscopy. The intrinsic anisotropies are unremarkable and are within the approximate range of 0.2 - 0.27. In cells, however, very interesting behavior is exhibited by meso-tetrahydroxyphenyl chlorin (mTHPC). Polarization-sensitive images of mTHPC's fluorescence show a pronounced banding of alternating high and low anisotropy consistent with an ordering of the sensitizer in the nuclear envelope, indicating that this structure is a target of photodynamic damage with this sensitizer. None of the other sensitizers exhibits localization to the nuclear envelope. The frequency distributions of the intracellular anisotropies of the sensitizers exhibit variable peaks and widths. An unusual case is that of Photofrin, with a peak in its anisotropy frequency distribution of -0.12. The change from a positive intrinsic anisotropy in homogeneous solution to a negative value in cells suggests an environmentally induced change in the relative orientations of the absorption and emission dipole moments.
引用
收藏
页码:1544 / 1547
页数:4
相关论文
共 19 条
[1]  
AXELROD D, 1989, FLUORESCENCE MICRO B, P333
[2]   Imaging enzyme activity with polarization-sensitive confocal fluorescence microscopy [J].
Bigelow, CE ;
Vishwasrao, HD ;
Frelinger, JG ;
Foster, TH .
JOURNAL OF MICROSCOPY, 2004, 215 (01) :24-33
[3]   Confocal fluorescence spectroscopy and anisotropy imaging system [J].
Bigelow, CE ;
Conover, DL ;
Foster, TH .
OPTICS LETTERS, 2003, 28 (09) :695-697
[4]   The orientation of eosin-5-maleimide on human erythrocyte band 3 measured by fluorescence polarization microscopy [J].
Blackman, SM ;
Cobb, CE ;
Beth, AH ;
Piston, DW .
BIOPHYSICAL JOURNAL, 1996, 71 (01) :194-208
[5]   Correlation between subcellular localization and photodynamic efficacy [J].
Kessel, D .
JOURNAL OF PORPHYRINS AND PHTHALOCYANINES, 2004, 8 (08) :1009-1014
[6]   Photophysical properties of meso, meso-linked porphyrin arrays: steady-state and time-resolved fluorescence polarization [J].
Kim, YH ;
Cho, HS ;
Kim, D ;
Kim, SK ;
Yoshida, N ;
Osuka, A .
SYNTHETIC METALS, 2001, 117 (1-3) :183-187
[7]  
Lakowicz J. R., 1999, PRINCIPLES FLUORESCE, P291, DOI DOI 10.1007/978-1-4757-3061-6_10
[8]   THE PHOTODEGRADATION OF PORPHYRINS IN CELLS CAN BE USED TO ESTIMATE THE LIFETIME OF SINGLET OXYGEN [J].
MOAN, J ;
BERG, K .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1991, 53 (04) :549-553
[9]  
Morris RL, 2003, CANCER RES, V63, P5194
[10]  
Niedre M, 2002, PHOTOCHEM PHOTOBIOL, V75, P382, DOI 10.1562/0031-8655(2002)075<0382:DNILDO>2.0.CO