Adhesive Photoswitch: Selective Photochemical Modulation of Enzymes under Physiological Conditions
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 inhib...
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Veröffentlicht in: | Journal of the American Chemical Society 2017-07, Vol.139 (29), p.10072-10078 |
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description | 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. |
doi_str_mv | 10.1021/jacs.7b05151 |
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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.</description><identifier>ISSN: 0002-7863</identifier><identifier>EISSN: 1520-5126</identifier><identifier>DOI: 10.1021/jacs.7b05151</identifier><identifier>PMID: 28675032</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Adhesives - chemistry ; Adhesives - pharmacology ; Azo Compounds - chemistry ; Azo Compounds - pharmacology ; Binding Sites - drug effects ; Carbonic Anhydrase Inhibitors - chemistry ; Carbonic Anhydrase Inhibitors - pharmacology ; Carbonic Anhydrases - metabolism ; Guanidine - chemistry ; Guanidine - pharmacology ; Molecular Structure ; Photochemical Processes ; Solubility ; Sulfonamides - chemistry ; Sulfonamides - pharmacology ; Surface Properties ; Water - chemistry</subject><ispartof>Journal of the American Chemical Society, 2017-07, Vol.139 (29), p.10072-10078</ispartof><rights>Copyright © 2017 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a427t-62aaed71792e5eb978266c2674e5a17f2d57bfaa429938e0cee33bfe8f0bc0c63</citedby><cites>FETCH-LOGICAL-a427t-62aaed71792e5eb978266c2674e5a17f2d57bfaa429938e0cee33bfe8f0bc0c63</cites><orcidid>0000-0002-0002-8017 ; 0000-0003-0445-6358</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/jacs.7b05151$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/jacs.7b05151$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2763,27075,27923,27924,56737,56787</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28675032$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mogaki, Rina</creatorcontrib><creatorcontrib>Okuro, Kou</creatorcontrib><creatorcontrib>Aida, Takuzo</creatorcontrib><title>Adhesive Photoswitch: Selective Photochemical Modulation of Enzymes under Physiological Conditions</title><title>Journal of the American Chemical Society</title><addtitle>J. Am. Chem. Soc</addtitle><description>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.</description><subject>Adhesives - chemistry</subject><subject>Adhesives - pharmacology</subject><subject>Azo Compounds - chemistry</subject><subject>Azo Compounds - pharmacology</subject><subject>Binding Sites - drug effects</subject><subject>Carbonic Anhydrase Inhibitors - chemistry</subject><subject>Carbonic Anhydrase Inhibitors - pharmacology</subject><subject>Carbonic Anhydrases - metabolism</subject><subject>Guanidine - chemistry</subject><subject>Guanidine - pharmacology</subject><subject>Molecular Structure</subject><subject>Photochemical Processes</subject><subject>Solubility</subject><subject>Sulfonamides - chemistry</subject><subject>Sulfonamides - pharmacology</subject><subject>Surface Properties</subject><subject>Water - chemistry</subject><issn>0002-7863</issn><issn>1520-5126</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkD1PwzAQhi0EoqWwMaOMDKTYTvwRtqoqHxIIJGCOHPtCXCVxiRNQ-fUktJSF6XSn597TPQidEjwlmJLLpdJ-KjLMCCN7aEwYxSEjlO-jMcaYhkLyaISOvF_2bUwlOUQjKrlgOKJjlM1MAd5-QPBUuNb5T9vq4ip4hhJ0uxvrAiqrVRk8ONOVqrWuDlweLOqvdQU-6GoDTU-uvXWle_sh5642dgD9MTrIVenhZFsn6PV68TK_De8fb-7ms_tQxVS0IadKgRFEJBQYZImQlHNNuYiBKSJyapjIctXDSRJJwBogirIcZI4zjTWPJuh8k7tq3HsHvk0r6zWUparBdT4lCWFSxpjEPXqxQXXjvG8gT1eNrVSzTglOB6vpYDXdWu3xs21yl1VgdvCvxr_Tw9bSdU3dP_p_1jft-4I8</recordid><startdate>20170726</startdate><enddate>20170726</enddate><creator>Mogaki, Rina</creator><creator>Okuro, Kou</creator><creator>Aida, Takuzo</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0002-8017</orcidid><orcidid>https://orcid.org/0000-0003-0445-6358</orcidid></search><sort><creationdate>20170726</creationdate><title>Adhesive Photoswitch: Selective Photochemical Modulation of Enzymes under Physiological Conditions</title><author>Mogaki, Rina ; Okuro, Kou ; Aida, Takuzo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a427t-62aaed71792e5eb978266c2674e5a17f2d57bfaa429938e0cee33bfe8f0bc0c63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adhesives - chemistry</topic><topic>Adhesives - pharmacology</topic><topic>Azo Compounds - chemistry</topic><topic>Azo Compounds - pharmacology</topic><topic>Binding Sites - drug effects</topic><topic>Carbonic Anhydrase Inhibitors - chemistry</topic><topic>Carbonic Anhydrase Inhibitors - pharmacology</topic><topic>Carbonic Anhydrases - metabolism</topic><topic>Guanidine - chemistry</topic><topic>Guanidine - pharmacology</topic><topic>Molecular Structure</topic><topic>Photochemical Processes</topic><topic>Solubility</topic><topic>Sulfonamides - chemistry</topic><topic>Sulfonamides - pharmacology</topic><topic>Surface Properties</topic><topic>Water - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mogaki, Rina</creatorcontrib><creatorcontrib>Okuro, Kou</creatorcontrib><creatorcontrib>Aida, Takuzo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the American Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mogaki, Rina</au><au>Okuro, Kou</au><au>Aida, Takuzo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adhesive Photoswitch: Selective Photochemical Modulation of Enzymes under Physiological Conditions</atitle><jtitle>Journal of the American Chemical Society</jtitle><addtitle>J. Am. Chem. Soc</addtitle><date>2017-07-26</date><risdate>2017</risdate><volume>139</volume><issue>29</issue><spage>10072</spage><epage>10078</epage><pages>10072-10078</pages><issn>0002-7863</issn><eissn>1520-5126</eissn><abstract>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.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>28675032</pmid><doi>10.1021/jacs.7b05151</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-0002-8017</orcidid><orcidid>https://orcid.org/0000-0003-0445-6358</orcidid></addata></record> |
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subjects | Adhesives - chemistry Adhesives - pharmacology Azo Compounds - chemistry Azo Compounds - pharmacology Binding Sites - drug effects Carbonic Anhydrase Inhibitors - chemistry Carbonic Anhydrase Inhibitors - pharmacology Carbonic Anhydrases - metabolism Guanidine - chemistry Guanidine - pharmacology Molecular Structure Photochemical Processes Solubility Sulfonamides - chemistry Sulfonamides - pharmacology Surface Properties Water - chemistry |
title | Adhesive Photoswitch: Selective Photochemical Modulation of Enzymes under Physiological Conditions |
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