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...

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Veröffentlicht in:Journal of medicinal chemistry 1995-05, Vol.38 (10), p.1751-1761
Hauptverfasser: Morelock, Maurice M, Pargellis, Christopher A, Graham, Edward T, Lamarre, Daniel, Jung, Grace
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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
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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 &amp; inhibitors</subject><subject>Renin - antagonists &amp; 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 &amp; inhibitors</topic><topic>Renin - antagonists &amp; 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>
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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
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