生物学中基于荧光蛋白的单原子离子传感器的设计与发展。

IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Kiheon Baek, Ke Ji, Weicheng Peng, Sureshee M Liyanaarachchi, Sheel C Dodani
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引用次数: 6

摘要

活细胞依赖于由阳离子和阴离子组成的无机离子梯度的精细调谐交响乐。这种微妙的平衡是由生物受体维持的,所有这些受体协同作用,选择性地识别和定位离子以实现体内平衡。这些动态过程可以使用基于荧光蛋白的生物传感器在生物体、组织、细胞和亚细胞水平上用光学显微镜截取和可视化。自1997年首次报道此类钙(Ca2+)工具以来,蛋白质工程及其相关领域的突出生物学问题和创新推动了Ca2+及其他新生物传感器的发展。在这篇综述中,我们总结了一种可用于生成基于荧光蛋白的生物传感器的工作流程,以研究生物学中的单原子离子。为了展示这种方法的范围,我们重点介绍了Ca2+生物传感器的最新进展,并详细讨论了过去四年中报道的钾(K+)、镁(Mg2+)、铜(Cu2+/+)、镧系元素(Ln3+)和氯(Cl-)离子生物传感器的代表性案例研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The design and evolution of fluorescent protein-based sensors for monoatomic ions in biology.

Living cells rely on a finely tuned symphony of inorganic ion gradients composed of both cations and anions. This delicate balance is maintained by biological receptors all acting in concert to selectively recognize and position ions for homeostasis. These dynamic processes can be intercepted and visualized with optical microscopy at the organismal, tissue, cellular and subcellular levels using fluorescent protein-based biosensors. Since the first report of such tool for calcium (Ca2+) in 1997, outstanding biological questions and innovations in protein engineering along with associated fields have driven the development of new biosensors for Ca2+ and beyond. In this Review, we summarize a workflow that can be used to generate fluorescent protein-based biosensors to study monoatomic ions in biology. To showcase the scope of this approach, we highlight recent advances reported for Ca2+ biosensors and in detail discuss representative case studies of biosensors reported in the last four years for potassium (K+), magnesium (Mg2+), copper (Cu2+/+), lanthanide (Ln3+) and chloride (Cl-) ions.

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来源期刊
Protein Engineering Design & Selection
Protein Engineering Design & Selection 生物-生化与分子生物学
CiteScore
3.30
自引率
4.20%
发文量
14
审稿时长
6-12 weeks
期刊介绍: Protein Engineering, Design and Selection (PEDS) publishes high-quality research papers and review articles relevant to the engineering, design and selection of proteins for use in biotechnology and therapy, and for understanding the fundamental link between protein sequence, structure, dynamics, function, and evolution.
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