首页> 外文期刊>Journal of the American Chemical Society >Adhesive Photoswitch: Selective Photochemical Modulation of Enzymes under Physiological Conditions
【24h】

Adhesive Photoswitch: Selective Photochemical Modulation of Enzymes under Physiological Conditions

机译:胶粘光电开关:在生理条件下酶的选择性光化学调节

获取原文
获取原文并翻译 | 示例
       

摘要

We developed a water-soluble adhesive photoswitch (Glue_n-Azo-SA, average n = 5) that selectively binds to a target enzyme and photochemically modulates its enzymatic activity even in cell lysates. Its design strategy features a photochromic azobenzene unit (Azo), which carries on one side an inhibitory motif for the target enzyme and on the other a glue part (Glue_n) that utilizes its multiple guanidinium ion (Gu~+) pendants for adhering onto the target surface. The target of Glue_n-Azo-SA is carbonic anhydrase (CA) because sulfonamide (SA) derivatives, such as SA at the terminus of Glue_n-Azo-SA, are known to bind selectively to the CA active site. The SA moiety, upon docking at the CA active site, possibly guides the connecting Glue_n part to an oxyanion-rich area in proximity to the active site for adhesion, so that the conjugation between Glue_n-Azo-SA and CA is ensured. With this geometry, the photochemical isomerization of the Azo unit likely generates a push-pull motion of SA, resulting in its docking and undocking at the active site of CA with the help of a competing substrate. Consequently, Glue_n-Azo-SA can selectively photomodulate the enzymatic action of CA even in cell lysates. Azo-SA without Glue_n can likewise suppress the enzymatic activity of CA by docking SA at its active site, but the resulting CA/Azo-SA conjugate, in contrast, does not respond to light.
机译:我们开发了一种水溶性粘合剂光敏开关(Glue_n-Azo-SA,平均n = 5),它选择性地结合到目标酶上,即使在细胞裂解液中也可以通过光化学方式调节其酶促活性。它的设计策略是使用光致变色的偶氮苯单元(Azo),其一侧带有目标酶的抑制性基序,另一侧带有胶水部分(Glue_n),该胶水部分利用其多个胍离子(Gu〜+)悬垂物粘附在分子上。目标表面。 Glue_n-Azo-SA的目标是碳酸酐酶(CA),因为已知磺酰胺(SA)衍生物(例如Glue_n-Azo-SA末端的SA)会选择性结合CA活性位点。 SA部分在对接于CA活性位点时,可能将连接的Glue_n部分引导至活性位点附近的富含氧阴离子的区域用于粘附,从而确保了Glue_n-Azo-SA与CA之间的缀合。在这种几何形状下,偶氮单元的光化学异构化可能会产生SA的推挽运动,从而在竞争性底物的帮助下使其在CA的活性位点对接和解扣。因此,即使在细胞裂解物中,Glue_n-Azo-SA也可以选择性地光调节CA的酶促作用。没有Glue_n的偶氮SA也可以通过将SA停靠在其活性位点来抑制CA的酶促活性,但是相反,所得的CA / Azo-SA共轭物对光没有反应。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2017年第29期|10072-10078|共7页
  • 作者单位

    Department of Chemistry and Biotechnology, School of Engineering, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, Japan;

    Department of Chemistry and Biotechnology, School of Engineering, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, Japan;

    Department of Chemistry and Biotechnology, School of Engineering, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, Japan,Riken Center for Emergent Matter Science, 2-1 Hirosawa, Wako, Saitama, Japan;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-18 03:08:01

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号