König K, Boehme S, Leclerc N, Ahuja R
Institute of Anatomy II, Friedrich Schiller University, Jena, Germany.
Cell Mol Biol (Noisy-le-grand). 1998 Jul;44(5):763-70.
Ultrafast time-gated fluorescence imaging of optically trapped single motile cells is presented. The biflagellar green microalga Haematococcus pluvialis was confined with picoNewton trapping forces in the focal volume of a high numerical aperture objective by near infrared multitraps. Trapping radiation of 100 mW power at the sample was provided by a Nd:YLF laser (1047 nm) operating in the cw mode. Simultaneously, cellular autofluorescence was excited with a 633 nm picosecond 80 MHz laser diode. An ultrafast gated intensified slow scan CCD camera system with a tunable gate width (200 ps-1 ms) and tunable time-delay (0-20 ns) between excitation and detection was used as fluorescence detector. We demonstrate fluorescence imaging of high temporal (sub-ns) and high spatial (sub-microm) resolution and fluorescence lifetime determination of intracellular autofluorescence based on chlorophyll excitation. Exposure to the herbicide DCMU resulted in an increase of fluorescence intensity and lifetime by 250% and 150%, respectively.
本文介绍了光学捕获单个运动细胞的超快时间门控荧光成像。双鞭毛绿微藻雨生红球藻通过近红外多重捕获以皮牛顿捕获力限制在高数值孔径物镜的焦体积内。样品处功率为100 mW的捕获辐射由连续波模式运行的Nd:YLF激光(1047 nm)提供。同时,用633 nm皮秒80 MHz激光二极管激发细胞自发荧光。使用具有可调门宽(200 ps - 1 ms)和激发与检测之间可调时间延迟(0 - 20 ns)的超快门控增强慢扫描CCD相机系统作为荧光探测器。我们展示了基于叶绿素激发的高时间(亚纳秒)和高空间(亚微米)分辨率的荧光成像以及细胞内自发荧光的荧光寿命测定。暴露于除草剂敌草隆导致荧光强度和寿命分别增加250%和150%。