{"title":"偶氮苯系DNA与T7 RNA聚合酶的反应及相互作用动力学","authors":"Gennosuke Takekawa, Yusuke Nakasone, Yukiko Kamiya, Hiroyuki Asanuma and Masahide Terazima","doi":"10.1039/D4CP04080E","DOIUrl":null,"url":null,"abstract":"<p >Reaction and interaction dynamics of azobenzene-tethered DNA (photoresponsive DNA) with T7 RNA polymerase (T7RNAP) were studied after photoisomerization of azobenzene from the <em>cis</em>- to <em>trans</em>-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 <em>cis</em>-AzoPBD within 1 ms, and this change is explained in terms of a structural change from a bent to an extended conformation upon the <em>cis</em>-to-<em>trans</em> photoisomerization. The association and dissociation rates of <em>cis</em>- and <em>trans</em>-AzoPBD–T7RNAP complex were measured by the fluorescence polarization measurements, and the dissociation constants for <em>cis</em>- and <em>trans</em>-AzoPBD were respectively determined to be 3.9 μM and 21 μM. The result indicates that <em>trans</em>-AzoPBD is dissociated upon photoexcitation of <em>cis</em>-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.</p>","PeriodicalId":99,"journal":{"name":"Physical Chemistry Chemical Physics","volume":" 6","pages":" 3302-3312"},"PeriodicalIF":2.9000,"publicationDate":"2025-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Reaction and interaction dynamics of azobenzene-tethered DNA with T7 RNA polymerase†\",\"authors\":\"Gennosuke Takekawa, Yusuke Nakasone, Yukiko Kamiya, Hiroyuki Asanuma and Masahide Terazima\",\"doi\":\"10.1039/D4CP04080E\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Reaction and interaction dynamics of azobenzene-tethered DNA (photoresponsive DNA) with T7 RNA polymerase (T7RNAP) were studied after photoisomerization of azobenzene from the <em>cis</em>- to <em>trans</em>-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 <em>cis</em>-AzoPBD within 1 ms, and this change is explained in terms of a structural change from a bent to an extended conformation upon the <em>cis</em>-to-<em>trans</em> photoisomerization. The association and dissociation rates of <em>cis</em>- and <em>trans</em>-AzoPBD–T7RNAP complex were measured by the fluorescence polarization measurements, and the dissociation constants for <em>cis</em>- and <em>trans</em>-AzoPBD were respectively determined to be 3.9 μM and 21 μM. The result indicates that <em>trans</em>-AzoPBD is dissociated upon photoexcitation of <em>cis</em>-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.</p>\",\"PeriodicalId\":99,\"journal\":{\"name\":\"Physical Chemistry Chemical Physics\",\"volume\":\" 6\",\"pages\":\" 3302-3312\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2025-01-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Physical Chemistry Chemical Physics\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/cp/d4cp04080e\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physical Chemistry Chemical Physics","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/cp/d4cp04080e","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
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.
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.
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