Becker Wolfgang, Shcheslavkiy Vladislav, Frere Samuel, Slutsky Inna
Becker & Hickl GmbH, Nahmitzer Damm 30, 12277, Berlin, Germany.
Microsc Res Tech. 2014 Mar;77(3):216-24. doi: 10.1002/jemt.22331. Epub 2014 Jan 13.
We present a technique that records transient changes in the fluorescence lifetime of a sample with spatial resolution along a one-dimensional scan. The technique is based on scanning the sample with a high-frequency pulsed laser beam, detecting single photons of the fluorescence light, and building up a photon distribution over the distance along the scan, the arrival times of the photons after the excitation pulses and the time after a stimulation of the sample. The maximum resolution at which lifetime changes can be recorded is given by the line scan period. Transient lifetime effects can thus be resolved at a resolution of about one millisecond. We demonstrate the technique for recording photochemical and nonphotochemical chlorophyll transients in plants and transient changes in free Ca(2+) in cultured neurons.
我们提出了一种技术,该技术可沿一维扫描以空间分辨率记录样品荧光寿命的瞬态变化。该技术基于用高频脉冲激光束扫描样品,检测荧光的单光子,并在沿扫描的距离上建立光子分布、激发脉冲后光子的到达时间以及样品受刺激后的时间。能够记录寿命变化的最大分辨率由线扫描周期给出。因此,瞬态寿命效应可以在约一毫秒的分辨率下得到解决。我们展示了该技术用于记录植物中的光化学和非光化学叶绿素瞬态以及培养神经元中游离Ca(2+)的瞬态变化。