利用双分子互补技术实现组蛋白修饰的活细胞可视化

IF 1.1 4区 化学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
A. I. Stepanov, L. V. Putlyaeva, A. A. Shuvaeva, M. A. Andrushkin, M. S. Baranov, N. G. Gurskaya, K. A. Lukyanov
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引用次数: 0

摘要

目的:组蛋白翻译后修饰(ptm)的研究是一个快速发展的领域,但可用于检测和解释这些修饰的工具有限。组蛋白修饰,如甲基化、乙酰化和磷酸化,在调节染色质动力学和基因表达中起着至关重要的作用。组蛋白修饰“读取器”结构域(HMRDs)的特异性结合是这一调控的核心,允许招募促进染色质重塑的蛋白质。本研究旨在开发基于hmrd的基因编码传感器来研究活细胞中的组蛋白修饰,为研究表观遗传变化提供一种更高效、更灵活的方法。方法:我们设计了基因编码传感器,利用HMRDs和splitFAST特异性结合不同的组蛋白修饰。这些传感器被整合到细胞中,以跟踪组蛋白修饰的动态变化。这些传感器的性能通过活细胞成像进行评估,使用荧光显微镜监测组蛋白修饰。结果和讨论:基因编码的传感器对各种组蛋白修饰表现出高特异性和敏感性。基于SplitFAST和HMRDs的传感器MPP8和AF9对H3K9me3和H3K9ac表现出特定的分布。此外,这两个结构域与SplitFAST不同部分的组合显示了H3K9me3和H3K9ac在空间上的接近性。这些发现表明,基于hmrd的传感器MPP8和AF9与SplitFAST的整合可以为活细胞监测组蛋白修饰及其在基因调控和细胞反应机制中的作用提供有价值的工具。结论:基于HMRDs的组蛋白修饰基因编码传感器的开发为研究活细胞中染色质动力学提供了一个强有力的新工具。这些传感器为了解组蛋白修饰的复杂机制及其对基因表达的影响提供了更直接和实时的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Live-Cell Visualization of Histone Modification Using Bimolecular Complementation

Live-Cell Visualization of Histone Modification Using Bimolecular Complementation

Objective: The study of histone post-translational modifications (PTMs) is a rapidly developing field, yet the tools available for detecting and interpreting these modifications are limited. Histone modifications, such as methylation, acetylation, and phosphorylation, play a crucial role in regulating chromatin dynamics and gene expression. Specific binding of histone modification “reader” domains (HMRDs) is central to this regulation, allowing for the recruitment of proteins that facilitate chromatin remodeling. This research aims to develop genetically encoded sensors based on HMRDs to study histone modifications in live cells, offering a more efficient and flexible method for studying epigenetic changes. Methods: We designed genetically encoded sensors that utilize HMRDs and splitFAST to bind specifically to different histone modifications. These sensors were incorporated into cells to track the dynamic changes in histone modifications. The performance of these sensors was evaluated through live-cell imaging, using fluorescent microscopy to monitor histone modifications. Results and Discussion: The genetically encoded sensors demonstrated high specificity and sensitivity to various histone modifications. Sensors based on SplitFAST and HMRDs MPP8 and AF9 exhibited specific distributions for H3K9me3 and H3K9ac. Moreover, the combination of these two domains with different parts of SplitFAST showed spatial proximity between H3K9me3 and H3K9ac. These findings suggest that the integration of HMRD-based sensors, MPP8 and AF9, with SplitFAST could provide valuable tools for live-cell monitoring of histone modifications and their roles in gene regulation and cellular response mechanisms. Conclusions: The development of genetically encoded sensors for histone modifications based on HMRDs provides a powerful new tool for studying chromatin dynamics in live cells. These sensors offer a more direct and real-time approach to understanding the complex mechanisms of histone modification and their impact on gene expression.

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来源期刊
Russian Journal of Bioorganic Chemistry
Russian Journal of Bioorganic Chemistry 生物-生化与分子生物学
CiteScore
1.80
自引率
10.00%
发文量
118
审稿时长
3 months
期刊介绍: Russian Journal of Bioorganic Chemistry publishes reviews and original experimental and theoretical studies on the structure, function, structure–activity relationships, and synthesis of biopolymers, such as proteins, nucleic acids, polysaccharides, mixed biopolymers, and their complexes, and low-molecular-weight biologically active compounds (peptides, sugars, lipids, antibiotics, etc.). The journal also covers selected aspects of neuro- and immunochemistry, biotechnology, and ecology.
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