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Investigation of binding between fluoroquinolones and pepsin by fluorescence spectroscopy and molecular simulation
In this paper, the interactions of pepsin with fluoroquinolones, including norfloxacin (NFX) or ofloxacin (OFX), were investigated using fluorescence spectroscopy. The effects of NFX or OFX on pepsin showed that the molecular conformation of pepsin and the microenvironment of tryptophan residues wer...
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Published in: | Luminescence (Chichester, England) England), 2019-09, Vol.34 (6), p.595-601 |
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creator | Lian, Shu‐Qin Lian, Jie Wang, Gui‐Rong Li, Lin Yang, Dong‐Zhi Xue, Yun‐sheng |
description | In this paper, the interactions of pepsin with fluoroquinolones, including norfloxacin (NFX) or ofloxacin (OFX), were investigated using fluorescence spectroscopy. The effects of NFX or OFX on pepsin showed that the molecular conformation of pepsin and the microenvironment of tryptophan residues were changed under mimicked physiological conditions. Static quenching was suggested as a factor. Quenching constants and binding constants were determined and thermodynamic parameters were calculated at three temperatures (25°C, 31°C and 37°C). Molecular interaction distances (binding distance r) were obtained. Binding was enthalpy driven and the process was spontaneous. Synchronous fluorescence, three‐dimensional fluorescence spectroscopy and molecular simulation were used for analysis. Interactions were further tested using molecular modelling. Quenching and binding constants of NFX with pepsin were the highest when testing NFX/OFX/fleroxacin/gatifloxacin with pepsin combinations. NFX was the strongest quencher, and affinity of NFX for pepsin was higher than that of OFX/fleroxacin/gatifloxacin. |
doi_str_mv | 10.1002/bio.3642 |
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The effects of NFX or OFX on pepsin showed that the molecular conformation of pepsin and the microenvironment of tryptophan residues were changed under mimicked physiological conditions. Static quenching was suggested as a factor. Quenching constants and binding constants were determined and thermodynamic parameters were calculated at three temperatures (25°C, 31°C and 37°C). Molecular interaction distances (binding distance r) were obtained. Binding was enthalpy driven and the process was spontaneous. Synchronous fluorescence, three‐dimensional fluorescence spectroscopy and molecular simulation were used for analysis. Interactions were further tested using molecular modelling. Quenching and binding constants of NFX with pepsin were the highest when testing NFX/OFX/fleroxacin/gatifloxacin with pepsin combinations. NFX was the strongest quencher, and affinity of NFX for pepsin was higher than that of OFX/fleroxacin/gatifloxacin.</description><identifier>ISSN: 1522-7235</identifier><identifier>EISSN: 1522-7243</identifier><identifier>DOI: 10.1002/bio.3642</identifier><identifier>PMID: 31074200</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Analytical methods ; Anti-Bacterial Agents - chemistry ; Binding ; Computer simulation ; Conformation ; Constants ; Enthalpy ; Fleroxacin ; Fleroxacin - chemistry ; Fluorescence ; Fluorescence spectroscopy ; Fluoroquinolones ; Fluoroquinolones - chemistry ; Gatifloxacin ; Kinetics ; Molecular Conformation ; Molecular Docking Simulation ; Molecular interactions ; Molecular modelling ; Norfloxacin ; Norfloxacin - chemistry ; Ofloxacin ; Pepsin ; Pepsin A - chemistry ; Physiological effects ; Protein Binding ; Quenching ; Simulation ; Spectrometry, Fluorescence ; Spectroscopy ; Spectrum analysis ; Tryptophan</subject><ispartof>Luminescence (Chichester, England), 2019-09, Vol.34 (6), p.595-601</ispartof><rights>2019 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3492-4638aa50f14923ea284ec9b0287edf227cc0a927ea34a8ad85e886f0ce2329733</citedby><cites>FETCH-LOGICAL-c3492-4638aa50f14923ea284ec9b0287edf227cc0a927ea34a8ad85e886f0ce2329733</cites><orcidid>0000-0002-5844-0020</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31074200$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lian, Shu‐Qin</creatorcontrib><creatorcontrib>Lian, Jie</creatorcontrib><creatorcontrib>Wang, Gui‐Rong</creatorcontrib><creatorcontrib>Li, Lin</creatorcontrib><creatorcontrib>Yang, Dong‐Zhi</creatorcontrib><creatorcontrib>Xue, Yun‐sheng</creatorcontrib><title>Investigation of binding between fluoroquinolones and pepsin by fluorescence spectroscopy and molecular simulation</title><title>Luminescence (Chichester, England)</title><addtitle>Luminescence</addtitle><description>In this paper, the interactions of pepsin with fluoroquinolones, including norfloxacin (NFX) or ofloxacin (OFX), were investigated using fluorescence spectroscopy. The effects of NFX or OFX on pepsin showed that the molecular conformation of pepsin and the microenvironment of tryptophan residues were changed under mimicked physiological conditions. Static quenching was suggested as a factor. Quenching constants and binding constants were determined and thermodynamic parameters were calculated at three temperatures (25°C, 31°C and 37°C). Molecular interaction distances (binding distance r) were obtained. Binding was enthalpy driven and the process was spontaneous. Synchronous fluorescence, three‐dimensional fluorescence spectroscopy and molecular simulation were used for analysis. Interactions were further tested using molecular modelling. Quenching and binding constants of NFX with pepsin were the highest when testing NFX/OFX/fleroxacin/gatifloxacin with pepsin combinations. NFX was the strongest quencher, and affinity of NFX for pepsin was higher than that of OFX/fleroxacin/gatifloxacin.</description><subject>Analytical methods</subject><subject>Anti-Bacterial Agents - chemistry</subject><subject>Binding</subject><subject>Computer simulation</subject><subject>Conformation</subject><subject>Constants</subject><subject>Enthalpy</subject><subject>Fleroxacin</subject><subject>Fleroxacin - chemistry</subject><subject>Fluorescence</subject><subject>Fluorescence spectroscopy</subject><subject>Fluoroquinolones</subject><subject>Fluoroquinolones - chemistry</subject><subject>Gatifloxacin</subject><subject>Kinetics</subject><subject>Molecular Conformation</subject><subject>Molecular Docking Simulation</subject><subject>Molecular interactions</subject><subject>Molecular modelling</subject><subject>Norfloxacin</subject><subject>Norfloxacin - chemistry</subject><subject>Ofloxacin</subject><subject>Pepsin</subject><subject>Pepsin A - chemistry</subject><subject>Physiological effects</subject><subject>Protein Binding</subject><subject>Quenching</subject><subject>Simulation</subject><subject>Spectrometry, Fluorescence</subject><subject>Spectroscopy</subject><subject>Spectrum analysis</subject><subject>Tryptophan</subject><issn>1522-7235</issn><issn>1522-7243</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp1kU9LxDAQxYMo7roKfgIJePHSNZmkbXpU8c-C4EXPJU2nEmmT2myV_fZm3XUFwdNMmB8vb-YRcsrZnDMGl5X1c5FJ2CNTngIkOUixv-tFOiFHIbwxxrIsKw7JRHCWS2BsSoaF-8CwtK96ab2jvqGVdbV1r7TC5Seio007-sG_j9b51jsMVLua9tgH62i12owxGHQGaejRLAcfjO9X31znWzRjqwcabBfr-pNjctDoNuDJts7Iy93t881D8vh0v7i5ekyMkAUkMhNK65Q1PL4EalASTVExUDnWDUBuDNMF5KiF1ErXKkWlsoYZBAFFLsSMXGx0-7X9uGTZ2eizbbVDP4YSQPAi5anII3r-B33z4-Ciu0gpWciUK_gVNHHFMGBT9oPt9LAqOSvXOZQxh3KdQ0TPtoJj1WG9A38OH4FkA3zaFlf_CpXXi6dvwS-wCpLm</recordid><startdate>201909</startdate><enddate>201909</enddate><creator>Lian, Shu‐Qin</creator><creator>Lian, Jie</creator><creator>Wang, Gui‐Rong</creator><creator>Li, Lin</creator><creator>Yang, Dong‐Zhi</creator><creator>Xue, Yun‐sheng</creator><general>Wiley Subscription Services, Inc</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>7QF</scope><scope>7QO</scope><scope>7QP</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>7U7</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F1W</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>H95</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L.G</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5844-0020</orcidid></search><sort><creationdate>201909</creationdate><title>Investigation of binding between fluoroquinolones and pepsin by fluorescence spectroscopy and molecular simulation</title><author>Lian, Shu‐Qin ; Lian, Jie ; Wang, Gui‐Rong ; Li, Lin ; Yang, Dong‐Zhi ; Xue, Yun‐sheng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3492-4638aa50f14923ea284ec9b0287edf227cc0a927ea34a8ad85e886f0ce2329733</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Analytical methods</topic><topic>Anti-Bacterial Agents - chemistry</topic><topic>Binding</topic><topic>Computer simulation</topic><topic>Conformation</topic><topic>Constants</topic><topic>Enthalpy</topic><topic>Fleroxacin</topic><topic>Fleroxacin - chemistry</topic><topic>Fluorescence</topic><topic>Fluorescence spectroscopy</topic><topic>Fluoroquinolones</topic><topic>Fluoroquinolones - chemistry</topic><topic>Gatifloxacin</topic><topic>Kinetics</topic><topic>Molecular Conformation</topic><topic>Molecular Docking Simulation</topic><topic>Molecular interactions</topic><topic>Molecular modelling</topic><topic>Norfloxacin</topic><topic>Norfloxacin - chemistry</topic><topic>Ofloxacin</topic><topic>Pepsin</topic><topic>Pepsin A - chemistry</topic><topic>Physiological effects</topic><topic>Protein Binding</topic><topic>Quenching</topic><topic>Simulation</topic><topic>Spectrometry, Fluorescence</topic><topic>Spectroscopy</topic><topic>Spectrum analysis</topic><topic>Tryptophan</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lian, Shu‐Qin</creatorcontrib><creatorcontrib>Lian, Jie</creatorcontrib><creatorcontrib>Wang, Gui‐Rong</creatorcontrib><creatorcontrib>Li, Lin</creatorcontrib><creatorcontrib>Yang, Dong‐Zhi</creatorcontrib><creatorcontrib>Xue, Yun‐sheng</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Toxicology Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Luminescence (Chichester, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lian, Shu‐Qin</au><au>Lian, Jie</au><au>Wang, Gui‐Rong</au><au>Li, Lin</au><au>Yang, Dong‐Zhi</au><au>Xue, Yun‐sheng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Investigation of binding between fluoroquinolones and pepsin by fluorescence spectroscopy and molecular simulation</atitle><jtitle>Luminescence (Chichester, England)</jtitle><addtitle>Luminescence</addtitle><date>2019-09</date><risdate>2019</risdate><volume>34</volume><issue>6</issue><spage>595</spage><epage>601</epage><pages>595-601</pages><issn>1522-7235</issn><eissn>1522-7243</eissn><abstract>In this paper, the interactions of pepsin with fluoroquinolones, including norfloxacin (NFX) or ofloxacin (OFX), were investigated using fluorescence spectroscopy. The effects of NFX or OFX on pepsin showed that the molecular conformation of pepsin and the microenvironment of tryptophan residues were changed under mimicked physiological conditions. Static quenching was suggested as a factor. Quenching constants and binding constants were determined and thermodynamic parameters were calculated at three temperatures (25°C, 31°C and 37°C). Molecular interaction distances (binding distance r) were obtained. Binding was enthalpy driven and the process was spontaneous. Synchronous fluorescence, three‐dimensional fluorescence spectroscopy and molecular simulation were used for analysis. Interactions were further tested using molecular modelling. Quenching and binding constants of NFX with pepsin were the highest when testing NFX/OFX/fleroxacin/gatifloxacin with pepsin combinations. NFX was the strongest quencher, and affinity of NFX for pepsin was higher than that of OFX/fleroxacin/gatifloxacin.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31074200</pmid><doi>10.1002/bio.3642</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-5844-0020</orcidid></addata></record> |
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subjects | Analytical methods Anti-Bacterial Agents - chemistry Binding Computer simulation Conformation Constants Enthalpy Fleroxacin Fleroxacin - chemistry Fluorescence Fluorescence spectroscopy Fluoroquinolones Fluoroquinolones - chemistry Gatifloxacin Kinetics Molecular Conformation Molecular Docking Simulation Molecular interactions Molecular modelling Norfloxacin Norfloxacin - chemistry Ofloxacin Pepsin Pepsin A - chemistry Physiological effects Protein Binding Quenching Simulation Spectrometry, Fluorescence Spectroscopy Spectrum analysis Tryptophan |
title | Investigation of binding between fluoroquinolones and pepsin by fluorescence spectroscopy and molecular simulation |
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