A mid-infrared laser microscope for the time-resolved study of light-induced protein conformational changes

被引:0
|
作者
Temperini, Maria Eleonora [1 ,2 ]
Polito, Raffaella [1 ]
Intze, Antonia [1 ,2 ]
Gillibert, Raymond [1 ]
Berkmann, Fritz [1 ]
Baldassarre, Leonetta [1 ]
Giliberti, Valeria [2 ]
Ortolani, Michele [1 ,2 ]
机构
[1] Sapienza Univ Rome, Dept Phys, Piazzale Aldo Moro 2, I-00185 Rome, Italy
[2] Ist Italiano Tecnol, Ctr Life Nano & Neuro Sci CL2NS, Viale Regina Elena 291, I-00161 Rome, Italy
来源
REVIEW OF SCIENTIFIC INSTRUMENTS | 2023年 / 94卷 / 06期
关键词
QUANTUM CASCADE LASERS; IR SPECTROSCOPY; BACTERIORHODOPSIN; DYNAMICS; INTERMEDIATE; RHODOPSINS;
D O I
10.1063/5.0136676
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
We have developed a confocal laser microscope operating in the mid-infrared range for the study of light-sensitive proteins, such as rhodopsins. The microscope features a co-aligned infrared and visible illumination path for the selective excitation and probing of proteins located in the IR focus only. An external-cavity tunable quantum cascade laser provides a wavelength tuning range (5.80-6.35 mu m or 1570-1724 cm(-1)) suitable for studying protein conformational changes as a function of time delay after visible light excitation with a pulsed LED. Using cryogen-free detectors, the relative changes in the infrared absorption of rhodopsin thin films around 10(-4) have been observed with a time resolution down to 30 ms. The measured full-width at half maximum of the Airy disk at lambda= 6.08 mu m in transmission mode with a confocal arrangement of apertures is 6.6 mu m or 1.1.. Dark-adapted sample replacement at the beginning of each photocycle is then enabled by exchanging the illuminated thin-film location with the microscope mapping stage synchronized to data acquisition and LED excitation and by averaging hundreds of time traces acquired in different nearby locations within a homogeneous film area. We demonstrate that this instrument provides crucial advantages for time-resolved IR studies of rhodopsin thin films with a slow photocycle. Time-resolved studies of inhomogeneous samples may also be possible with the presented instrument.
引用
收藏
页数:9
相关论文
共 24 条
  • [21] Elucidation of the nature of the conformational changes of the EF-interhelical loop in bacteriorhodopsin and of the helix VIII on the cytoplasmic surface of bovine rhodopsin:: A time-resolved fluorescence depolarization study
    Alexiev, U
    Rimke, I
    Pöhlmann, T
    JOURNAL OF MOLECULAR BIOLOGY, 2003, 328 (03) : 705 - 719
  • [22] Toward Better Efficiency of Air-Stable Polyazomethine-Based Organic Solar Cells Using Time-Resolved Photoluminescence and Light-Induced Electron Spin Resonance as Verification Methods
    Ciechanowicz, Sylwia Grankowska
    Korona, Krzysztof P.
    Wolos, Agnieszka
    Drabinska, Aneta
    Iwan, Agnieszka
    Tazbir, Igor
    Wojtkiewicz, Jacek
    Kaminska, Maria
    JOURNAL OF PHYSICAL CHEMISTRY C, 2016, 120 (21): : 11415 - 11425
  • [23] High hydrostatic pressure-induced conformational changes in protein disulfide oxidoreductase from the hyperthermophilic archaeon Pyrococcus furiosus. A Fourier-transform infrared spectroscopic study
    Scire, Andrea
    Pedone, Emilia
    Ausili, Alessio
    Saviano, Michele
    Baldassarre, Maurizio
    Bertoli, Enrico
    Bartolucci, Simonetta
    Tanfani, Fabio
    MOLECULAR BIOSYSTEMS, 2010, 6 (10) : 2015 - 2022
  • [24] Formation of CN Radical from Nitrogen and Carbon Condensation and from Photodissociation in Femtosecond Laser-Induced Plasmas: Time-Resolved FT-UV-Vis Spectroscopic Study of the Violet Emission of CN Radical
    Mogyorosi, K.
    Sarosi, K.
    Seres, I
    Jojart, P.
    Fule, M.
    Chikan, V
    JOURNAL OF PHYSICAL CHEMISTRY A, 2020, 124 (14): : 2755 - 2767