INSERM, U603, Paris F-75006, France.
J Neurosci Methods. 2011 Jun 15;198(2):172-80. doi: 10.1016/j.jneumeth.2011.03.015. Epub 2011 Mar 30.
Low-magnification high-numerical aperture objectives maximize the collection efficiency for scattered two-photon excited fluorescence (2PEF), but non-descanned detection schemes for such objectives demand optical components much bigger than standard microscope optics. Fiber coupling offers the possibility of removing bulky multi-channel detectors from the collection site, but coupling and transmission losses are generally believed to outweigh the benefits of optical fibers. We present here two new developments based on large-core fiber-optic fluorescence detection that illustrate clear advantages over conventional air-coupled 2PEF detection schemes. First, with minimal modifications of a commercial microscope, we efficiently couple the output of a 20×/NA0.95 objective to a large-core liquid light guide and we obtain a 7-fold collection gain when imaging astrocytes at 100 μm depth in acute brain slices of adult ALDH1L1-GFP mice. Second, combining 2PEF microscopy and 4-color detection on a custom microscope, mode scrambling inside a 2-mm plastic optical fiber is shown to cancel out the spatially non-uniform spectral sensitivity observed with air-coupled detectors. Spectral unmixing of images of brainbow mice taken with a fiber-coupled detector revealed a uniform color distribution of hippocampal neurons across a large field of view. Thus, fiber coupling improves both the efficiency and the homogeneity of 2PEF collection.
低倍放大高数值孔径物镜最大限度地提高了散射双光子激发荧光(2PEF)的收集效率,但对于此类物镜的非扫描检测方案需要比标准显微镜光学元件大得多的光学元件。光纤耦合提供了从收集点去除大型多通道探测器的可能性,但耦合和传输损耗通常被认为超过了光纤的优势。我们在这里介绍了两种基于大芯光纤荧光检测的新发展,它们清楚地证明了优于传统空气耦合 2PEF 检测方案的优势。首先,通过对商用显微镜进行最小的修改,我们可以有效地将 20×/NA0.95 物镜的输出耦合到大芯液体光导中,并且在对成年 ALDH1L1-GFP 小鼠急性脑切片中 100 μm 深度的星形胶质细胞进行成像时,我们获得了 7 倍的收集增益。其次,在定制显微镜上结合 2PEF 显微镜和 4 色检测,显示在 2mm 塑料光纤内的模式混频可以消除与空气耦合探测器观察到的空间非均匀光谱灵敏度。用光纤耦合探测器拍摄的 brainbow 小鼠的图像的光谱解混显示出海马神经元在大视场中均匀的颜色分布。因此,光纤耦合提高了 2PEF 收集的效率和均匀性。