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通过带像散成像的时间聚焦多光子显微镜进行动态粒子追踪

Dynamic particle tracking via temporal focusing multiphoton microscopy with astigmatism imaging.

作者信息

Lien Chi-Hsiang, Lin Chun-Yu, Chen Shean-Jen, Chien Fan-Ching

出版信息

Opt Express. 2014 Nov 3;22(22):27290-9. doi: 10.1364/OE.22.027290.

Abstract

A three-dimensional (3D) single fluorescent particle tracking strategy based on temporal focusing multiphoton excitation microscopy (TFMPEM) combined with astigmatism imaging is proposed for delivering nanoscale-level axial information that reveals 3D trajectories of single fluorospheres in the axially-resolved multiphoton excitation volume without z-axis scanning. Whereas other scanning spatial focusing multiphoton excitation schemes induce optical trapping interference, temporal focusing multiphoton excitation produces widefield illumination with minimum optical trapping force on the fluorospheres. Currently, the lateral and axial positioning resolutions of the dynamic particle tracking approach are about 14 nm and 21 nm in standard deviation, respectively. Furthermore, the motion behavior and diffusion coefficients of fluorospheres in glycerol solutions with different concentrations are dynamically measured at a frame rate up to 100 Hz. This TFMPEM with astigmatism imaging holds great promise for exploring dynamic molecular behavior deep inside biotissues via its superior penetration, reduced trapping effect, fast frame rate, and nanoscale-level positioning.

摘要

提出了一种基于时间聚焦多光子激发显微镜(TFMPEM)与像散成像相结合的三维(3D)单荧光粒子跟踪策略,用于提供纳米级轴向信息,该信息可揭示轴向分辨多光子激发体积内单个荧光球的3D轨迹,而无需进行z轴扫描。与其他扫描空间聚焦多光子激发方案会产生光阱干扰不同,时间聚焦多光子激发产生的是宽场照明,对荧光球的光阱力最小。目前,动态粒子跟踪方法的横向和轴向定位分辨率的标准偏差分别约为14 nm和21 nm。此外,还以高达100 Hz的帧率动态测量了不同浓度甘油溶液中荧光球的运动行为和扩散系数。这种带有像散成像的TFMPEM凭借其卓越的穿透能力、降低的捕获效应、快速的帧率和纳米级定位,在探索生物组织深处的动态分子行为方面具有巨大潜力。

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