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通过影子链杂交驱动的置换工程实现可调pH开关的合理设计。

Rational design of tunable pH switches through shadow-strand hybridization-actuated displacement engineering.

作者信息

Han Xiaole, Dong Xiangyu, Lin Xiaomei, Yu Hongyan, Zhang Li, Wang Weitao, Zhang Yaoyi, Jiang Jianbo, Liu Xingyu, Yang Gang, Guo Yongcan, Xie Guoming

机构信息

Key Laboratory of Clinical Laboratory Diagnostics (Chinese Ministry of Education), College of Laboratory Medicine, Chongqing Medical University, Chongqing 400016, P. R. China.

Department of Neurosurgery, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, P. R. China.

出版信息

Nucleic Acids Res. 2025 Sep 5;53(17). doi: 10.1093/nar/gkaf849.

DOI:10.1093/nar/gkaf849
PMID:40923757
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12412784/
Abstract

Local pH variations play a pivotal role in numerous critical biological processes. However, achieving the tunability and selectivity of pH detection remains a challenge. Here, we present a DNA-based strategy that enables programmable and selective pH responses, which is termed shadow-strand hybridization-actuated displacement engineering (SHADE). The tunability of pH responses is accomplished via rational manipulations of shadow strands derived from the i-motif-forming sequence. Shadow strands, which can be considered the "nucleic acid molecular chaperones," assist in the folding of i-motif structure under acidic conditions via toehold-mediated strand displacement reactions (TMSDR). The response to alkaline conditions is achieved through a hairpin shadow (HS) containing A+-C pairs in stem. Combining i-motif-forming sequence and HS allows for the development of a narrow pH-responsive probe. Furthermore, aptamer was conjugated to guide the probe on cell surfaces. The pH sensitivity of SHADE allows for significant fluorescence enhancement in acidic tumor microenvironments, thereby improving the signal-to-noise ratio in vivo imaging. This work represents the application of TMSDR programmability to pH regulation. The SHADE strategy holds promise beyond pH sensing, potentially enabling the manipulation of diverse quadruplex architectures and facilitating the creation of highly responsive components for synthetic molecular devices and signal transduction networks.

摘要

局部pH值变化在众多关键生物过程中起着关键作用。然而,实现pH检测的可调性和选择性仍然是一个挑战。在此,我们提出了一种基于DNA的策略,该策略能够实现可编程和选择性的pH响应,称为影子链杂交驱动的置换工程(SHADE)。pH响应的可调性是通过对源自i-基序形成序列的影子链进行合理操作来实现的。影子链可被视为“核酸分子伴侣”,在酸性条件下通过链置换介导的链置换反应(TMSDR)协助i-基序结构的折叠。通过在茎中含有A+-C对的发夹影子(HS)实现对碱性条件的响应。将i-基序形成序列和HS相结合,可开发出窄pH响应探针。此外,还连接了适体以引导探针在细胞表面定位。SHADE的pH敏感性可在酸性肿瘤微环境中实现显著的荧光增强,从而提高体内成像的信噪比。这项工作代表了TMSDR可编程性在pH调节中的应用。SHADE策略在pH传感之外还有望发挥作用,有可能实现对各种四链体结构的操控,并有助于为合成分子器件和信号转导网络创建高响应性组件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/366b/12412784/6da306bf12fa/gkaf849fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/366b/12412784/1e65089d7667/gkaf849figgra1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/366b/12412784/976a7343592a/gkaf849fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/366b/12412784/67053f305af6/gkaf849fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/366b/12412784/0f642f81b25d/gkaf849fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/366b/12412784/aad946eade2d/gkaf849fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/366b/12412784/6da306bf12fa/gkaf849fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/366b/12412784/1e65089d7667/gkaf849figgra1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/366b/12412784/976a7343592a/gkaf849fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/366b/12412784/67053f305af6/gkaf849fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/366b/12412784/0f642f81b25d/gkaf849fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/366b/12412784/aad946eade2d/gkaf849fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/366b/12412784/6da306bf12fa/gkaf849fig5.jpg

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