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基于紧凑型共聚焦扫描头的双光子显微镜和光谱学。

Two-photon microscopy and spectroscopy based on a compact confocal scanning head.

作者信息

Diaspro A, Chirico G, Federici F, Cannone F, Beretta S, Robello M

机构信息

University of Genoa, National Institute for the Physics of Matter (INFM), Department of Physics, Via Dodecaneso 33, 16146 Genova, Italy.

出版信息

J Biomed Opt. 2001 Jul;6(3):300-10. doi: 10.1117/1.1382809.

Abstract

We have combined a confocal laser scanning head modified for TPE (two-photon excitation) microscopy with some spectroscopic modules to study single molecules and molecular aggregates. The behavior of the TPE microscope unit has been characterized by means of point spread function measurements and of the demonstration of its micropatterning abilities. One-photon and two-photon mode can be simply accomplished by switching from a mono-mode optical fiber (one-photon) coupled to conventional laser sources to an optical module that allows IR laser beam (two-photon/TPE) delivery to the confocal laser scanning head. We have then described the characterization of the two-photon microscope for spectroscopic applications: fluorescence correlation, lifetime and fluorescence polarization anisotropy measurements. We describe the measurement of the response of the two-photon microscope to the light polarization and discuss fluorescence polarization anisotropy measurements on Rhodamine 6G as a function of the viscosity and on a globular protein, the Beta-lactoglobulin B labeled with Alexa 532 at very high dilutions. The average rotational and translational diffusion coefficients measured with fluorescence polarization anisotropy and fluorescence correlation methods are in good agreement with the protein size, therefore validating the use of the microscope for two-photon spectroscopy on biomolecules.

摘要

我们将一个为双光子激发(TPE)显微镜改装的共聚焦激光扫描头与一些光谱模块相结合,用于研究单分子和分子聚集体。通过点扩散函数测量及其微图案化能力的展示,对TPE显微镜单元的性能进行了表征。单光子和双光子模式可以通过简单地从耦合到传统激光源的单模光纤(单光子)切换到允许红外激光束(双光子/TPE)传输到共聚焦激光扫描头的光学模块来实现。然后,我们描述了用于光谱应用的双光子显微镜的特性:荧光相关、寿命和荧光偏振各向异性测量。我们描述了双光子显微镜对光偏振的响应测量,并讨论了在罗丹明6G上作为粘度函数以及在非常高稀释度下用Alexa 532标记的球状蛋白β-乳球蛋白B上的荧光偏振各向异性测量。用荧光偏振各向异性和荧光相关方法测量的平均旋转和平移扩散系数与蛋白质大小吻合良好,因此验证了该显微镜用于生物分子双光子光谱的可行性。

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