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细胞生物发光成像

Cellular bioluminescence imaging.

作者信息

Welsh David K, Noguchi Takako

出版信息

Cold Spring Harb Protoc. 2012 Aug 1;2012(8):pdb.top070607. doi: 10.1101/pdb.top070607.

Abstract

Bioluminescence imaging of live cells has recently been recognized as an important alternative to fluorescence imaging. Fluorescent probes are much brighter than bioluminescent probes (luciferase enzymes) and, therefore, provide much better spatial and temporal resolution and much better contrast for delineating cell structure. However, with bioluminescence imaging there is virtually no background or toxicity. As a result, bioluminescence can be superior to fluorescence for detecting and quantifying molecules and their interactions in living cells, particularly in long-term studies. Structurally diverse luciferases from beetle and marine species have been used for a wide variety of applications, including tracking cells in vivo, detecting protein-protein interactions, measuring levels of calcium and other signaling molecules, detecting protease activity, and reporting circadian clock gene expression. Such applications can be optimized by the use of brighter and variously colored luciferases, brighter microscope optics, and ultrasensitive, low-noise cameras. This article presents a review of how bioluminescence differs from fluorescence, its applications to cellular imaging, and available probes, optics, and detectors. It also gives practical suggestions for optimal bioluminescence imaging of single cells.

摘要

活细胞的生物发光成像最近已被公认为荧光成像的一种重要替代方法。荧光探针比生物发光探针(荧光素酶)亮得多,因此,在描绘细胞结构方面提供了更好的空间和时间分辨率以及更好的对比度。然而,生物发光成像几乎没有背景或毒性。因此,在检测和定量活细胞中的分子及其相互作用时,尤其是在长期研究中,生物发光可能优于荧光。来自甲虫和海洋物种的结构多样的荧光素酶已被用于广泛的应用,包括体内追踪细胞、检测蛋白质-蛋白质相互作用、测量钙和其他信号分子的水平、检测蛋白酶活性以及报告生物钟基因表达。通过使用更亮、颜色各异的荧光素酶、更亮的显微镜光学器件以及超灵敏、低噪声相机,可以优化此类应用。本文综述了生物发光与荧光的不同之处、其在细胞成像中的应用以及可用的探针、光学器件和探测器。它还给出了单细胞最佳生物发光成像的实用建议。

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