TY - JOUR
T1 - Development of a novel cryogenic microscope with numerical aperture of 0.9 and its application to photosynthesis research
AU - Shibata, Yutaka
AU - Katoh, Wataru
AU - Chiba, Tomofumi
AU - Namie, Keisuke
AU - Ohnishi, Norikazu
AU - Minagawa, Jun
AU - Nakanishi, Hanayo
AU - Noguchi, Takumi
AU - Fukumura, Hiroshi
N1 - Funding Information:
We are grateful to Prof. Yasuhiro Kashino and Dr. Natsuko Inoue-Kashino at the University of Hyogo for kindly providing us the His-tagged PsaL strain of Synechocystis sp. PCC 6803. Y.S. and W.K. are deeply grateful to Mr. Masumi Katsuki at the Technical Center of Nagoya University for expert advice on the manufacture of the microscope system. This work was supported in part by Grants-in-Aid for Scientific Research (Nos. 21750017 and 24370060 to Y.S.), the 21st COE program for “the origin of the universe and matter” from the Japanese Ministry of Education, Culture, Sports, Science, and Technology (MEXT), and the Japan Society for the Promotion of Science (JSPS).
PY - 2014/6
Y1 - 2014/6
N2 - A novel cryogenic optical-microscope system was developed in which the objective lens is set inside of the cryostat adiabatic vacuum space. Being isolated from the sample when it was cooled, the objective lens was maintained at room temperature during the cryogenic measurement. Therefore, the authors were able to use a color-aberration corrected objective lens with a numerical aperture of 0.9. The lens is equipped with an air vent for compatibility to the vacuum. The theoretically expected spatial resolutions of 0.39 μm along the lateral direction and 1.3 μm along the axial direction were achieved by the developed system. The system was applied to the observations of non-uniform distributions of the photosystems in the cells of a green alga, Chlamydomonas reinhardtii, at 94 K. Gaussian decomposition analysis of the fluorescence spectra at all the pixels clearly demonstrated a non-uniform distribution of the two photosystems, as reflected in the variable ratios of the fluorescence intensities assigned to photosystem II and to those assigned to photosystem I. The system was also applied to the fluorescence spectroscopy of single isolated photosystem I complexes at 90 K. The fluorescence, assigned to be emitted from a single photosystem I trimer, showed an intermittent fluctuation called blinking, which is typical for a fluorescence signal from a single molecule. The vibronic fluorescence bands at around 790 nm were observed for single photosystem I trimers, suggesting that the color aberration is not serious up to the 800 nm spectral region.
AB - A novel cryogenic optical-microscope system was developed in which the objective lens is set inside of the cryostat adiabatic vacuum space. Being isolated from the sample when it was cooled, the objective lens was maintained at room temperature during the cryogenic measurement. Therefore, the authors were able to use a color-aberration corrected objective lens with a numerical aperture of 0.9. The lens is equipped with an air vent for compatibility to the vacuum. The theoretically expected spatial resolutions of 0.39 μm along the lateral direction and 1.3 μm along the axial direction were achieved by the developed system. The system was applied to the observations of non-uniform distributions of the photosystems in the cells of a green alga, Chlamydomonas reinhardtii, at 94 K. Gaussian decomposition analysis of the fluorescence spectra at all the pixels clearly demonstrated a non-uniform distribution of the two photosystems, as reflected in the variable ratios of the fluorescence intensities assigned to photosystem II and to those assigned to photosystem I. The system was also applied to the fluorescence spectroscopy of single isolated photosystem I complexes at 90 K. The fluorescence, assigned to be emitted from a single photosystem I trimer, showed an intermittent fluctuation called blinking, which is typical for a fluorescence signal from a single molecule. The vibronic fluorescence bands at around 790 nm were observed for single photosystem I trimers, suggesting that the color aberration is not serious up to the 800 nm spectral region.
KW - Chlamydomonas reinhardtii
KW - Fluorescence blinking
KW - Lateral heterogeneity of photosystem
KW - Photosystem I
KW - Single-molecule spectroscopy
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U2 - 10.1016/j.bbabio.2014.03.006
DO - 10.1016/j.bbabio.2014.03.006
M3 - Article
C2 - 24650629
AN - SCOPUS:84896690913
SN - 0005-2728
VL - 1837
SP - 880
EP - 887
JO - Biochimica et Biophysica Acta - Bioenergetics
JF - Biochimica et Biophysica Acta - Bioenergetics
IS - 6
ER -