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定量单分子定位显微镜技术

Quantitative Single-Molecule Localization Microscopy.

机构信息

Department of Physiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA; email:

Department of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

出版信息

Annu Rev Biophys. 2023 May 9;52:139-160. doi: 10.1146/annurev-biophys-111622-091212.

Abstract

Super-resolution fluorescence microscopy allows the investigation of cellular structures at nanoscale resolution using light. Current developments in super-resolution microscopy have focused on reliable quantification of the underlying biological data. In this review, we first describe the basic principles of super-resolution microscopy techniques such as stimulated emission depletion (STED) microscopy and single-molecule localization microscopy (SMLM), and then give a broad overview of methodological developments to quantify super-resolution data, particularly those geared toward SMLM data. We cover commonly used techniques such as spatial point pattern analysis, colocalization, and protein copy number quantification but also describe more advanced techniques such as structural modeling, single-particle tracking, and biosensing. Finally, we provide an outlook on exciting new research directions to which quantitative super-resolution microscopy might be applied.

摘要

超分辨率荧光显微镜利用光线实现了对细胞结构的纳米级分辨率研究。目前,超分辨率显微镜的发展重点是可靠地定量分析潜在的生物数据。在这篇综述中,我们首先描述了超分辨率显微镜技术的基本原理,如受激发射损耗(STED)显微镜和单分子定位显微镜(SMLM),然后广泛概述了定量超分辨率数据的方法学发展,特别是针对 SMLM 数据的方法学发展。我们涵盖了常用的技术,如空间点模式分析、共定位和蛋白质拷贝数定量,但也描述了更先进的技术,如结构建模、单颗粒跟踪和生物传感。最后,我们展望了定量超分辨率显微镜可能应用的令人兴奋的新研究方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb91/11268362/25e8d2f2d1cd/nihms-2008698-f0001.jpg

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