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基于适体的 DNA 变构开关调控蛋白质活性。

Aptamer-Based DNA Allosteric Switch for Regulation of Protein Activity.

机构信息

College of Chemistry, Institute of Analytical Chemistry for Life Science, Zhengzhou University, Zhengzhou, 450001, China.

The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, China.

出版信息

Adv Sci (Weinh). 2024 Aug;11(30):e2402531. doi: 10.1002/advs.202402531. Epub 2024 Jun 12.

Abstract

Allostery is a fundamental way to regulate the function of biomolecules playing crucial roles in cell metabolism and proliferation and is deemed the second secret of life. Given the limited understanding of the structure of natural allosteric molecules, the development of artificial allosteric molecules brings a huge opportunity to transform the allosteric mechanism into practical applications. In this study, the concept of bionics is introduced into the design of artificial allosteric molecules and an allosteric DNA switch with an activity site and an allosteric site based on two aptamers for selective inhibition of thrombin activity. Compared with the single aptamer, the allosteric switch possesses a significantly enhanced inhibition ability, which can be precisely regulated by converting the switch states. Moreover, the dynamic allosteric switch is further subjected to the control of the DNA threshold circuit for realizing automatic concentration determination and activity inhibition of thrombin. These compelling results confirm that this allosteric switch equipped with self-sensing and information-processing modules puts a new slant on the research of allosteric mechanisms and further application of allosteric tactics in chemical and biomedical fields.

摘要

变构作用是调节生物分子功能的一种基本方式,在细胞代谢和增殖中起着至关重要的作用,被认为是生命的第二大奥秘。鉴于对天然变构分子结构的有限了解,人工变构分子的发展为将变构机制转化为实际应用带来了巨大的机会。在这项研究中,仿生学的概念被引入到人工变构分子的设计中,设计了一种基于两个适体的具有活性位点和变构位点的变构 DNA 开关,用于选择性抑制凝血酶活性。与单个适体相比,变构开关具有显著增强的抑制能力,并且可以通过转换开关状态来精确调节。此外,动态变构开关进一步受到 DNA 门控电路的控制,用于实现凝血酶的自动浓度测定和活性抑制。这些令人信服的结果证实,这种配备了自我感应和信息处理模块的变构开关为变构机制的研究和进一步将变构策略应用于化学和生物医学领域提供了新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c05a/11321679/f13271943dae/ADVS-11-2402531-g001.jpg

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