偶氮苯系DNA与T7 RNA聚合酶的反应及相互作用动力学

IF 2.9 3区 化学 Q3 CHEMISTRY, PHYSICAL
Gennosuke Takekawa, Yusuke Nakasone, Yukiko Kamiya, Hiroyuki Asanuma and Masahide Terazima
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引用次数: 0

摘要

利用瞬态光栅(TG)和时间分辨荧光偏振技术研究了偶氮苯顺式到反式光异构化后,偶氮苯系DNA(光响应DNA)与T7RNAP的反应和相互作用动力学。检测了两种类型的光响应DNA: AzoPBD,拴在蛋白质结合位点,AzoTATA,拴在解绕位点。顺式偶氮opbd在光激发后1 ms内发生了扩散变化,这种变化可以用顺式到反式光异构化过程中从弯曲构象到扩展构象的结构变化来解释。通过荧光偏振测量测定了顺式和反式azopbd - t7rnap配合物的缔合速率和解离速率,确定了顺式和反式azopbd的解离常数分别为3.9 μM和21 μM。结果表明,在顺式- azopbd - t7rnap配合物的光激发下,反式- azopbd被解离。有效的解离主要是由较小的缔合速率常数引起的。时间分辨扩散测量结果显示,T7RNAP的浓度决定了构象变化的时间常数为2.4 ms,解离反应的速率较慢。虽然AzoTATA在异构化过程中没有表现出明显的结构变化,但在AzoTATA - t7rnap的光激发下观察到扩散变化。其起源归因于AzoTATA从解绕到闭合状态的变化,但AzoTATA不与T7RNAP分离。这些发现强调了偶氮苯插入位置在调节DNA-T7RNAP相互作用动力学中的关键作用,为光调控转录控制提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Reaction and interaction dynamics of azobenzene-tethered DNA with T7 RNA polymerase†

Reaction and interaction dynamics of azobenzene-tethered DNA with T7 RNA polymerase†

Reaction and interaction dynamics of azobenzene-tethered DNA with T7 RNA polymerase†

Reaction and interaction dynamics of azobenzene-tethered DNA (photoresponsive DNA) with T7 RNA polymerase (T7RNAP) were studied after photoisomerization of azobenzene from the cis- to trans-forms using the transient grating (TG) and time-resolved fluorescence polarization techniques. Two types of photoresponsive DNA were examined: AzoPBD, tethered at the protein binding site, and AzoTATA, tethered at the unwinding site. A diffusion change was observed after photoexcitation of cis-AzoPBD within 1 ms, and this change is explained in terms of a structural change from a bent to an extended conformation upon the cis-to-trans photoisomerization. The association and dissociation rates of cis- and trans-AzoPBD–T7RNAP complex were measured by the fluorescence polarization measurements, and the dissociation constants for cis- and trans-AzoPBD were respectively determined to be 3.9 μM and 21 μM. The result indicates that trans-AzoPBD is dissociated upon photoexcitation of cis-AzoPBD–T7RNAP complex. The efficient dissociation is mainly caused by a small association rate constant. The time-resolved diffusion measurement showed a conformational change with a time constant of 2.4 ms and a dissociation reaction with a slower rate, which depends on the concentration of T7RNAP. Although AzoTATA does not exhibit significant structural changes upon isomerization, a diffusion change was observed upon photoexcitation of AzoTATA–T7RNAP. The origin is attributed to changes from the unwound to closed states of AzoTATA, but AzoTATA does not dissociate from T7RNAP. These findings highlight a critical role of the azobenzene insertion position in modulating DNA–T7RNAP interaction dynamics, providing new insights into light-regulated transcription control.

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来源期刊
Physical Chemistry Chemical Physics
Physical Chemistry Chemical Physics 化学-物理:原子、分子和化学物理
CiteScore
5.50
自引率
9.10%
发文量
2675
审稿时长
2.0 months
期刊介绍: Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.
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