Time-Resolved Ligand Exchange Reactions: Kinetic Models for Competitive Inhibitors with Recombinant Human Renin
The on and off rate constants (kon and koff) were determined for a series of peptidomimetic, competitive inhibitors of human renin using a novel binding assay. The method entails analyzing a pair of ligand exchange reactions in which a dansylated inhibitor serves as the fluorescent probe. The first...
Gespeichert in:
Veröffentlicht in: | Journal of medicinal chemistry 1995-05, Vol.38 (10), p.1751-1761 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1761 |
---|---|
container_issue | 10 |
container_start_page | 1751 |
container_title | Journal of medicinal chemistry |
container_volume | 38 |
creator | Morelock, Maurice M Pargellis, Christopher A Graham, Edward T Lamarre, Daniel Jung, Grace |
description | The on and off rate constants (kon and koff) were determined for a series of peptidomimetic, competitive inhibitors of human renin using a novel binding assay. The method entails analyzing a pair of ligand exchange reactions in which a dansylated inhibitor serves as the fluorescent probe. The first in the pair of reactions involves preincubating renin with the probe and initiating the reaction by addition of a sample inhibitor; the second reaction involves preincubating renin with the sample inhibitor and initiating the reaction by addition of probe. Both reactions yield progress curves which contain complementary information concerning the kon and koff of each ligand. The two curves are fitted simultaneously using models derived from the differential rate equations describing the ligand exchange process. The kon and koff rate constants for the probe were 6.85 x 10(6) M-1 s-1 and 2.96 x 10(-4) s-1, respectively, giving a calculated Kd of 43.2 pM. The Kd values for the inhibitor series varied over 2 orders of magnitude (27-2320 pM), while the individual kon (10(6)-10(7) M-1 s-1) and koff (10(-4)-10(-3) s-1) constants varied only over 1 order of magnitude. |
doi_str_mv | 10.1021/jm00010a019 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_77276165</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>77276165</sourcerecordid><originalsourceid>FETCH-LOGICAL-a383t-1569d44400ff96b61303e994f3aaa69194a449602e340c1aa6c7cc895aaf91a43</originalsourceid><addsrcrecordid>eNpt0M1rFDEYBvAgSl2rJ89CDqIHGc3XZCa9ydLa4hZLXcFbeDeT6WadSdYkU9v_vim7LB56CjzvLy_Jg9BbSj5TwuiXzUgIoQQIVc_QjNaMVKIl4jmaEcJYxSTjL9GrlDaFccr4ETpqmppR1c5QWLrRVtc2heHWdnjhbsB3-PTOrMHfWHxtwWQXfDrB35232Rl8GTo7JNyHiOdh3JYsu1uLL_zarVwOMeF_Lq_LTRPGlfPgMz6fRvAl8c6_Ri96GJJ9sz-P0a-z0-X8vFr8-HYx_7qogLc8V7SWqhNCENL3Sq4k5YRbpUTPAUAqqgQIoSRhlgtiaMlMY0yraoBeURD8GH3Y7d3G8HeyKevRJWOHAbwNU9JNwxpJZV3gpx00MaQUba-30Y0Q7zUl-rFe_V-9Rb_br51Wo-0Odt9nmb_fzyEZGPoI3rh0YLwuv6tlYdWOuZTt3WEM8Y-WDW9qvbz6qc_YnJP296W-Kv7jzoNJehOm6Et3Tz7wAWu1nSo</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>77276165</pqid></control><display><type>article</type><title>Time-Resolved Ligand Exchange Reactions: Kinetic Models for Competitive Inhibitors with Recombinant Human Renin</title><source>MEDLINE</source><source>American Chemical Society Journals</source><creator>Morelock, Maurice M ; Pargellis, Christopher A ; Graham, Edward T ; Lamarre, Daniel ; Jung, Grace</creator><creatorcontrib>Morelock, Maurice M ; Pargellis, Christopher A ; Graham, Edward T ; Lamarre, Daniel ; Jung, Grace</creatorcontrib><description>The on and off rate constants (kon and koff) were determined for a series of peptidomimetic, competitive inhibitors of human renin using a novel binding assay. The method entails analyzing a pair of ligand exchange reactions in which a dansylated inhibitor serves as the fluorescent probe. The first in the pair of reactions involves preincubating renin with the probe and initiating the reaction by addition of a sample inhibitor; the second reaction involves preincubating renin with the sample inhibitor and initiating the reaction by addition of probe. Both reactions yield progress curves which contain complementary information concerning the kon and koff of each ligand. The two curves are fitted simultaneously using models derived from the differential rate equations describing the ligand exchange process. The kon and koff rate constants for the probe were 6.85 x 10(6) M-1 s-1 and 2.96 x 10(-4) s-1, respectively, giving a calculated Kd of 43.2 pM. The Kd values for the inhibitor series varied over 2 orders of magnitude (27-2320 pM), while the individual kon (10(6)-10(7) M-1 s-1) and koff (10(-4)-10(-3) s-1) constants varied only over 1 order of magnitude.</description><identifier>ISSN: 0022-2623</identifier><identifier>EISSN: 1520-4804</identifier><identifier>DOI: 10.1021/jm00010a019</identifier><identifier>PMID: 7752198</identifier><identifier>CODEN: JMCMAR</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Analytical, structural and metabolic biochemistry ; Binding, Competitive ; Biological and medical sciences ; Enzymes and enzyme inhibitors ; Fundamental and applied biological sciences. Psychology ; Humans ; Hydrolases ; Kinetics ; Ligands ; Recombinant Proteins - antagonists & inhibitors ; Renin - antagonists & inhibitors ; Spectrometry, Fluorescence ; Time Factors</subject><ispartof>Journal of medicinal chemistry, 1995-05, Vol.38 (10), p.1751-1761</ispartof><rights>1995 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a383t-1569d44400ff96b61303e994f3aaa69194a449602e340c1aa6c7cc895aaf91a43</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/jm00010a019$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/jm00010a019$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3538356$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7752198$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Morelock, Maurice M</creatorcontrib><creatorcontrib>Pargellis, Christopher A</creatorcontrib><creatorcontrib>Graham, Edward T</creatorcontrib><creatorcontrib>Lamarre, Daniel</creatorcontrib><creatorcontrib>Jung, Grace</creatorcontrib><title>Time-Resolved Ligand Exchange Reactions: Kinetic Models for Competitive Inhibitors with Recombinant Human Renin</title><title>Journal of medicinal chemistry</title><addtitle>J. Med. Chem</addtitle><description>The on and off rate constants (kon and koff) were determined for a series of peptidomimetic, competitive inhibitors of human renin using a novel binding assay. The method entails analyzing a pair of ligand exchange reactions in which a dansylated inhibitor serves as the fluorescent probe. The first in the pair of reactions involves preincubating renin with the probe and initiating the reaction by addition of a sample inhibitor; the second reaction involves preincubating renin with the sample inhibitor and initiating the reaction by addition of probe. Both reactions yield progress curves which contain complementary information concerning the kon and koff of each ligand. The two curves are fitted simultaneously using models derived from the differential rate equations describing the ligand exchange process. The kon and koff rate constants for the probe were 6.85 x 10(6) M-1 s-1 and 2.96 x 10(-4) s-1, respectively, giving a calculated Kd of 43.2 pM. The Kd values for the inhibitor series varied over 2 orders of magnitude (27-2320 pM), while the individual kon (10(6)-10(7) M-1 s-1) and koff (10(-4)-10(-3) s-1) constants varied only over 1 order of magnitude.</description><subject>Analytical, structural and metabolic biochemistry</subject><subject>Binding, Competitive</subject><subject>Biological and medical sciences</subject><subject>Enzymes and enzyme inhibitors</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Hydrolases</subject><subject>Kinetics</subject><subject>Ligands</subject><subject>Recombinant Proteins - antagonists & inhibitors</subject><subject>Renin - antagonists & inhibitors</subject><subject>Spectrometry, Fluorescence</subject><subject>Time Factors</subject><issn>0022-2623</issn><issn>1520-4804</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpt0M1rFDEYBvAgSl2rJ89CDqIHGc3XZCa9ydLa4hZLXcFbeDeT6WadSdYkU9v_vim7LB56CjzvLy_Jg9BbSj5TwuiXzUgIoQQIVc_QjNaMVKIl4jmaEcJYxSTjL9GrlDaFccr4ETpqmppR1c5QWLrRVtc2heHWdnjhbsB3-PTOrMHfWHxtwWQXfDrB35232Rl8GTo7JNyHiOdh3JYsu1uLL_zarVwOMeF_Lq_LTRPGlfPgMz6fRvAl8c6_Ri96GJJ9sz-P0a-z0-X8vFr8-HYx_7qogLc8V7SWqhNCENL3Sq4k5YRbpUTPAUAqqgQIoSRhlgtiaMlMY0yraoBeURD8GH3Y7d3G8HeyKevRJWOHAbwNU9JNwxpJZV3gpx00MaQUba-30Y0Q7zUl-rFe_V-9Rb_br51Wo-0Odt9nmb_fzyEZGPoI3rh0YLwuv6tlYdWOuZTt3WEM8Y-WDW9qvbz6qc_YnJP296W-Kv7jzoNJehOm6Et3Tz7wAWu1nSo</recordid><startdate>19950501</startdate><enddate>19950501</enddate><creator>Morelock, Maurice M</creator><creator>Pargellis, Christopher A</creator><creator>Graham, Edward T</creator><creator>Lamarre, Daniel</creator><creator>Jung, Grace</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</scope><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></search><sort><creationdate>19950501</creationdate><title>Time-Resolved Ligand Exchange Reactions: Kinetic Models for Competitive Inhibitors with Recombinant Human Renin</title><author>Morelock, Maurice M ; Pargellis, Christopher A ; Graham, Edward T ; Lamarre, Daniel ; Jung, Grace</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a383t-1569d44400ff96b61303e994f3aaa69194a449602e340c1aa6c7cc895aaf91a43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Analytical, structural and metabolic biochemistry</topic><topic>Binding, Competitive</topic><topic>Biological and medical sciences</topic><topic>Enzymes and enzyme inhibitors</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Hydrolases</topic><topic>Kinetics</topic><topic>Ligands</topic><topic>Recombinant Proteins - antagonists & inhibitors</topic><topic>Renin - antagonists & inhibitors</topic><topic>Spectrometry, Fluorescence</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Morelock, Maurice M</creatorcontrib><creatorcontrib>Pargellis, Christopher A</creatorcontrib><creatorcontrib>Graham, Edward T</creatorcontrib><creatorcontrib>Lamarre, Daniel</creatorcontrib><creatorcontrib>Jung, Grace</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><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 medicinal chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Morelock, Maurice M</au><au>Pargellis, Christopher A</au><au>Graham, Edward T</au><au>Lamarre, Daniel</au><au>Jung, Grace</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Time-Resolved Ligand Exchange Reactions: Kinetic Models for Competitive Inhibitors with Recombinant Human Renin</atitle><jtitle>Journal of medicinal chemistry</jtitle><addtitle>J. Med. Chem</addtitle><date>1995-05-01</date><risdate>1995</risdate><volume>38</volume><issue>10</issue><spage>1751</spage><epage>1761</epage><pages>1751-1761</pages><issn>0022-2623</issn><eissn>1520-4804</eissn><coden>JMCMAR</coden><abstract>The on and off rate constants (kon and koff) were determined for a series of peptidomimetic, competitive inhibitors of human renin using a novel binding assay. The method entails analyzing a pair of ligand exchange reactions in which a dansylated inhibitor serves as the fluorescent probe. The first in the pair of reactions involves preincubating renin with the probe and initiating the reaction by addition of a sample inhibitor; the second reaction involves preincubating renin with the sample inhibitor and initiating the reaction by addition of probe. Both reactions yield progress curves which contain complementary information concerning the kon and koff of each ligand. The two curves are fitted simultaneously using models derived from the differential rate equations describing the ligand exchange process. The kon and koff rate constants for the probe were 6.85 x 10(6) M-1 s-1 and 2.96 x 10(-4) s-1, respectively, giving a calculated Kd of 43.2 pM. The Kd values for the inhibitor series varied over 2 orders of magnitude (27-2320 pM), while the individual kon (10(6)-10(7) M-1 s-1) and koff (10(-4)-10(-3) s-1) constants varied only over 1 order of magnitude.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>7752198</pmid><doi>10.1021/jm00010a019</doi><tpages>11</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0022-2623 |
ispartof | Journal of medicinal chemistry, 1995-05, Vol.38 (10), p.1751-1761 |
issn | 0022-2623 1520-4804 |
language | eng |
recordid | cdi_proquest_miscellaneous_77276165 |
source | MEDLINE; American Chemical Society Journals |
subjects | Analytical, structural and metabolic biochemistry Binding, Competitive Biological and medical sciences Enzymes and enzyme inhibitors Fundamental and applied biological sciences. Psychology Humans Hydrolases Kinetics Ligands Recombinant Proteins - antagonists & inhibitors Renin - antagonists & inhibitors Spectrometry, Fluorescence Time Factors |
title | Time-Resolved Ligand Exchange Reactions: Kinetic Models for Competitive Inhibitors with Recombinant Human Renin |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-30T01%3A32%3A52IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Time-Resolved%20Ligand%20Exchange%20Reactions:%20Kinetic%20Models%20for%20Competitive%20Inhibitors%20with%20Recombinant%20Human%20Renin&rft.jtitle=Journal%20of%20medicinal%20chemistry&rft.au=Morelock,%20Maurice%20M&rft.date=1995-05-01&rft.volume=38&rft.issue=10&rft.spage=1751&rft.epage=1761&rft.pages=1751-1761&rft.issn=0022-2623&rft.eissn=1520-4804&rft.coden=JMCMAR&rft_id=info:doi/10.1021/jm00010a019&rft_dat=%3Cproquest_cross%3E77276165%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=77276165&rft_id=info:pmid/7752198&rfr_iscdi=true |