分子荧光团的多光子激发截面

Chris Xu, Rebecca M. Williams, W. Zipfel, W. Webb
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引用次数: 153

摘要

通过分子吸收来自锁模激光紧密聚焦飞秒脉冲的两个或三个近红外光子的荧光团的非线性激发,为细胞生物学家提供了前所未有的用于显微成像和细胞分析的生物分子指标。测量25个紫外和可见光吸收荧光团的双光子激发光谱,从690到1050 nm,揭示了近红外激发的有用横截面,为活生物制剂提供了艺术家的发射标记,化学指标和天然细胞吸收剂的调色板。三光子荧光团激发光谱的测量现在建议相对良性的波长激发更深的紫外线荧光团。聚焦非线性激励固有的光学切片能力为成像提供了三维分辨率,并避免了失焦背景。描述了测量的非线性激发光谱,并定义了非线性显微镜对生物成像的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multiphoton excitation cross‐sections of molecular fluorophores
Nonlinear excitation of fluorophores through molecular absorption of two or three near-infra-red photons from the tightly focused femtosecond pulses of a mode-locked laser offers the cellular biologist an unprecedented panoply of biomolecular indicators for microscopic imaging and cellular analysis. Measurements of the two-photon excitation spectra of 25 ultra-violet and visible absorbing fluorophores from 690 to 1050 nm reveal useful cross sections for near infra-red excitation, providing an artist's palette of emission markers, chemical indicators, and native cellular absorbers for living biological preparations. Measurements of three-photon fluorophore excitation spectra now suggest relatively benign wavelengths to excite deeper UV fluorophores. The inherent optical sectioning capabilities of focused nonlinear excitation provides three-dimensional resolution for imaging and avoids out-of-focus background. Measured nonlinear excitation spectra are described and implications to nonlinear microscopy for biological imaging are defined.
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