Fluorescent labeling strategies for molecular bioimaging.

IF 2.4 Q3 BIOPHYSICS
Biophysical reports Pub Date : 2025-03-12 Epub Date: 2025-02-12 DOI:10.1016/j.bpr.2025.100200
Marcel Streit, Made Budiarta, Marvin Jungblut, Gerti Beliu
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引用次数: 0

Abstract

Super-resolution microscopy (SRM) has transformed biological imaging by circumventing the diffraction limit of light and enabling the visualization of cellular structures and processes at the molecular level. Central to the capabilities of SRM is fluorescent labeling, which ensures the precise attachment of fluorophores to biomolecules and has direct impact on the accuracy and resolution of imaging. Continuous innovation and optimization in fluorescent labeling are essential for the successful application of SRM in cutting-edge biological research. In this review, we discuss recent advances in fluorescent labeling strategies for molecular bioimaging, with a special focus on protein labeling. We compare different approaches, highlight technological breakthroughs, and address challenges such as linkage error and labeling density. By evaluating both established and emerging methods, we aim to guide researchers through all aspects that should be considered before opting for any labeling technique.

分子生物成像的荧光标记策略。
超分辨率显微镜(SRM)通过绕过光的衍射极限,在分子水平上实现细胞结构和过程的可视化,改变了生物成像。SRM的核心功能是荧光标记,它确保了荧光团与生物分子的精确连接,并直接影响成像的准确性和分辨率。荧光标记的不断创新和优化是SRM在前沿生物学研究中成功应用的关键。在这篇综述中,我们讨论了分子生物成像荧光标记策略的最新进展,特别关注蛋白质标记。我们比较了不同的方法,强调了技术突破,并解决了链接错误和标签密度等挑战。通过评估既建立和新兴的方法,我们的目标是指导研究人员通过应考虑的所有方面之前选择任何标记技术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biophysical reports
Biophysical reports Biophysics
CiteScore
2.40
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0.00%
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审稿时长
75 days
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