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Fast objective coupled planar illumination microscopy

机译:快速物镜耦合平面照明显微镜

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Among optical imaging techniques light sheet fluorescence microscopy is one of the most attractive for capturing high-speed biological dynamics unfolding in three dimensions. The technique is potentially millions of times faster than point-scanning techniques such as two-photon microscopy. However light sheet microscopes are limited by volume scanning rate and/or camera speed. We present speed-optimized Objective Coupled Planar Illumination (OCPI) microscopy, a fast light sheet technique that avoids compromising image quality or photon efficiency. Our fast scan system supports 40?Hz imaging of 700?μm-thick volumes if camera speed is sufficient. We also address the camera speed limitation by introducing Distributed Planar Imaging (DPI), a scaleable technique that parallelizes image acquisition across cameras. Finally, we demonstrate fast calcium imaging of the larval zebrafish brain and find a heartbeat-induced artifact, removable when the imaging rate exceeds 15?Hz. These advances extend the reach of fluorescence microscopy for monitoring fast processes in large volumes.
机译:在光学成像技术中,光片荧光显微镜是最吸引人的捕获在三维中的高速生物动力学中最具吸引力之一。该技术可能比点扫描技术(例如二光子显微镜)速度快倍数。然而,光板显微镜受到体积扫描速率和/或摄像机速度的限制。我们呈现速度优化的物镜耦合平面照明(OCPI)显微镜,一种快速的光片技术,避免了图像质量或光子效率。如果相机速度足够,我们的快速扫描系统支持40次700?μm厚的卷。我们还通过引入分布式平面成像(DPI),一种可扩展技术来解决摄像机速度限制,该技术并将图像采集平行于摄像机。最后,我们展示了幼虫斑马鱼脑的快速钙成像,并在成像速率超过15Ω·赫兹时发现心跳诱导的伪影。这些进步扩展了荧光显微镜的覆盖作用,以监测大量的快速过程。

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