Competition between solution and cell surface receptors for ligand. Dissociation of hapten bound to surface antibody in the presence of solution antibody
We present a joint theoretical and experimental study on the effects of competition for ligand between receptors in solution and receptors on cell surfaces. We focus on the following experiment. After ligand and cell surface receptors equilibrate, solution receptors are introduced, and the dissociat...
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Veröffentlicht in: | Biophysical journal 1989-11, Vol.56 (5), p.955-966 |
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creator | Goldstein, B. Posner, R.G. Torney, D.C. Erickson, J. Holowka, D. Baird, B. |
description | We present a joint theoretical and experimental study on the effects of competition for ligand between receptors in solution and receptors on cell surfaces. We focus on the following experiment. After ligand and cell surface receptors equilibrate, solution receptors are introduced, and the dissociation of surface bound ligand is monitored. We derive theoretical expressions for the dissociation rate and compare with experiment. In a standard dissociation experiment (no solution receptors present) dissociation may be slowed by rebinding, i.e., at high receptor densities a ligand that dissociates from one receptor may rebind to other receptors before separating from the cell. Our theory predicts that rebinding will be prevented when S much greater than N2Kon/(16 pi 2D a4), where S is the free receptor site concentration in solution, N the number of free surface receptor sites per cell, Kon the forward rate constant for ligand-receptor binding in solution, D the diffusion coefficient of the ligand, and a the cell radius. The predicted concentration of solution receptors needed to prevent rebinding is proportional to the square of the cell surface receptor density. The experimental system used in these studies consists of a monovalent ligand, 2,4-dinitrophenyl (DNP)-aminocaproyl-L-tyrosine (DCT), that reversibly binds to a monoclonal anti-DNP immunoglobulin E (IgE). This IgE is both a solution receptor and, when anchored to its high affinity Fc epsilon receptor on rat basophilic leukemia (RBL) cells, a surface receptor. For RBL cells with 6 x 10(5) binding sites per cell, our theory predicts that to prevent DCT rebinding to cell surface IgE during dissociation requires S much greater than 2,400 nM. We show that for S = 200–1,700 nM, the dissociation rate of DCT from surface IgE is substantially slower than from solution IgE where no rebinding occurs. Other predictions are also tested and shown to be consistent with experiment. |
doi_str_mv | 10.1016/S0006-3495(89)82741-9 |
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Dissociation of hapten bound to surface antibody in the presence of solution antibody</title><source>MEDLINE</source><source>Cell Press Free Archives</source><source>Elsevier ScienceDirect Journals</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Goldstein, B. ; Posner, R.G. ; Torney, D.C. ; Erickson, J. ; Holowka, D. ; Baird, B.</creator><creatorcontrib>Goldstein, B. ; Posner, R.G. ; Torney, D.C. ; Erickson, J. ; Holowka, D. ; Baird, B.</creatorcontrib><description>We present a joint theoretical and experimental study on the effects of competition for ligand between receptors in solution and receptors on cell surfaces. We focus on the following experiment. After ligand and cell surface receptors equilibrate, solution receptors are introduced, and the dissociation of surface bound ligand is monitored. We derive theoretical expressions for the dissociation rate and compare with experiment. In a standard dissociation experiment (no solution receptors present) dissociation may be slowed by rebinding, i.e., at high receptor densities a ligand that dissociates from one receptor may rebind to other receptors before separating from the cell. Our theory predicts that rebinding will be prevented when S much greater than N2Kon/(16 pi 2D a4), where S is the free receptor site concentration in solution, N the number of free surface receptor sites per cell, Kon the forward rate constant for ligand-receptor binding in solution, D the diffusion coefficient of the ligand, and a the cell radius. The predicted concentration of solution receptors needed to prevent rebinding is proportional to the square of the cell surface receptor density. The experimental system used in these studies consists of a monovalent ligand, 2,4-dinitrophenyl (DNP)-aminocaproyl-L-tyrosine (DCT), that reversibly binds to a monoclonal anti-DNP immunoglobulin E (IgE). This IgE is both a solution receptor and, when anchored to its high affinity Fc epsilon receptor on rat basophilic leukemia (RBL) cells, a surface receptor. For RBL cells with 6 x 10(5) binding sites per cell, our theory predicts that to prevent DCT rebinding to cell surface IgE during dissociation requires S much greater than 2,400 nM. We show that for S = 200–1,700 nM, the dissociation rate of DCT from surface IgE is substantially slower than from solution IgE where no rebinding occurs. Other predictions are also tested and shown to be consistent with experiment.</description><identifier>ISSN: 0006-3495</identifier><identifier>EISSN: 1542-0086</identifier><identifier>DOI: 10.1016/S0006-3495(89)82741-9</identifier><identifier>PMID: 2532552</identifier><identifier>CODEN: BIOJAU</identifier><language>eng</language><publisher>Bethesda, MD: Elsevier Inc</publisher><subject>Animals ; Antigens, Differentiation, B-Lymphocyte - metabolism ; Binding, Competitive ; Biological and medical sciences ; Cell Line ; Cell Membrane - immunology ; Cell receptors ; Cell structures and functions ; Fundamental and applied biological sciences. Psychology ; Haptens ; Immunoglobulin E - metabolism ; Kinetics ; Leukemia, Basophilic, Acute - immunology ; Leukemia, Experimental - immunology ; Ligands ; Mathematics ; Miscellaneous ; Models, Theoretical ; Molecular and cellular biology ; Rats ; Receptors, Fc - metabolism ; Receptors, IgE ; Solutions</subject><ispartof>Biophysical journal, 1989-11, Vol.56 (5), p.955-966</ispartof><rights>1989 The Biophysical Society</rights><rights>1991 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c523t-ee7d1e92f97c2dba70aa890322d25aced5f6110449bc6ee1695c4bb17718f53b3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1280594/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0006349589827419$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,3537,27901,27902,53766,53768,65534</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19459833$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2532552$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Goldstein, B.</creatorcontrib><creatorcontrib>Posner, R.G.</creatorcontrib><creatorcontrib>Torney, D.C.</creatorcontrib><creatorcontrib>Erickson, J.</creatorcontrib><creatorcontrib>Holowka, D.</creatorcontrib><creatorcontrib>Baird, B.</creatorcontrib><title>Competition between solution and cell surface receptors for ligand. Dissociation of hapten bound to surface antibody in the presence of solution antibody</title><title>Biophysical journal</title><addtitle>Biophys J</addtitle><description>We present a joint theoretical and experimental study on the effects of competition for ligand between receptors in solution and receptors on cell surfaces. We focus on the following experiment. After ligand and cell surface receptors equilibrate, solution receptors are introduced, and the dissociation of surface bound ligand is monitored. We derive theoretical expressions for the dissociation rate and compare with experiment. In a standard dissociation experiment (no solution receptors present) dissociation may be slowed by rebinding, i.e., at high receptor densities a ligand that dissociates from one receptor may rebind to other receptors before separating from the cell. Our theory predicts that rebinding will be prevented when S much greater than N2Kon/(16 pi 2D a4), where S is the free receptor site concentration in solution, N the number of free surface receptor sites per cell, Kon the forward rate constant for ligand-receptor binding in solution, D the diffusion coefficient of the ligand, and a the cell radius. The predicted concentration of solution receptors needed to prevent rebinding is proportional to the square of the cell surface receptor density. The experimental system used in these studies consists of a monovalent ligand, 2,4-dinitrophenyl (DNP)-aminocaproyl-L-tyrosine (DCT), that reversibly binds to a monoclonal anti-DNP immunoglobulin E (IgE). This IgE is both a solution receptor and, when anchored to its high affinity Fc epsilon receptor on rat basophilic leukemia (RBL) cells, a surface receptor. For RBL cells with 6 x 10(5) binding sites per cell, our theory predicts that to prevent DCT rebinding to cell surface IgE during dissociation requires S much greater than 2,400 nM. We show that for S = 200–1,700 nM, the dissociation rate of DCT from surface IgE is substantially slower than from solution IgE where no rebinding occurs. Other predictions are also tested and shown to be consistent with experiment.</description><subject>Animals</subject><subject>Antigens, Differentiation, B-Lymphocyte - metabolism</subject><subject>Binding, Competitive</subject><subject>Biological and medical sciences</subject><subject>Cell Line</subject><subject>Cell Membrane - immunology</subject><subject>Cell receptors</subject><subject>Cell structures and functions</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Haptens</subject><subject>Immunoglobulin E - metabolism</subject><subject>Kinetics</subject><subject>Leukemia, Basophilic, Acute - immunology</subject><subject>Leukemia, Experimental - immunology</subject><subject>Ligands</subject><subject>Mathematics</subject><subject>Miscellaneous</subject><subject>Models, Theoretical</subject><subject>Molecular and cellular biology</subject><subject>Rats</subject><subject>Receptors, Fc - metabolism</subject><subject>Receptors, IgE</subject><subject>Solutions</subject><issn>0006-3495</issn><issn>1542-0086</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUk1vFCEYJsamrtWf0ISLRg_TAjPMwEVj1q8mTXpQz4SBd7qYWRiBqelP8d_K7G7WeuqJhOfr5X1A6JySC0poe_mNENJWdSP5GyHfCtY1tJJP0IryhlWEiPYpWh0pz9DzlH4SQhkn9BSdMl4zztkK_VmH7QTZZRc87iH_BvA4hXHeXWhvsYFxxGmOgzaAIxiYcogJDyHi0d0WxgX-6FIKxumdJgx4o6dcbPowF30OR7X22fXB3mPncd4AniIk8AUomgeZe9ILdDLoMcHLw3mGfnz-9H39tbq--XK1_nBdGc7qXAF0loJkg-wMs73uiNZCkpoxy3gJtXxoKSVNI3vTAtBWctP0Pe06KgZe9_UZerf3neZ-C9aAz1GPaopuq-O9Ctqp_xHvNuo23CnKBOGyKQavDwYx_JohZbV1adma9hDmpDrZUNFx-SixNCeklKIQ-Z5oYkgpwnCchhK1lK925aulWSWk2pWvloDzh085qg5tF_zVAdfJ6HGI2huX_pnLhpf0uvDe73lQ9n7nIKpk3FKUdeUDZGWDe2SSv4_I0NQ</recordid><startdate>19891101</startdate><enddate>19891101</enddate><creator>Goldstein, B.</creator><creator>Posner, R.G.</creator><creator>Torney, D.C.</creator><creator>Erickson, J.</creator><creator>Holowka, D.</creator><creator>Baird, B.</creator><general>Elsevier Inc</general><general>Biophysical Society</general><scope>6I.</scope><scope>AAFTH</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>7QL</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M81</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19891101</creationdate><title>Competition between solution and cell surface receptors for ligand. Dissociation of hapten bound to surface antibody in the presence of solution antibody</title><author>Goldstein, B. ; Posner, R.G. ; Torney, D.C. ; Erickson, J. ; Holowka, D. ; Baird, B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c523t-ee7d1e92f97c2dba70aa890322d25aced5f6110449bc6ee1695c4bb17718f53b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Animals</topic><topic>Antigens, Differentiation, B-Lymphocyte - metabolism</topic><topic>Binding, Competitive</topic><topic>Biological and medical sciences</topic><topic>Cell Line</topic><topic>Cell Membrane - immunology</topic><topic>Cell receptors</topic><topic>Cell structures and functions</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Haptens</topic><topic>Immunoglobulin E - metabolism</topic><topic>Kinetics</topic><topic>Leukemia, Basophilic, Acute - immunology</topic><topic>Leukemia, Experimental - immunology</topic><topic>Ligands</topic><topic>Mathematics</topic><topic>Miscellaneous</topic><topic>Models, Theoretical</topic><topic>Molecular and cellular biology</topic><topic>Rats</topic><topic>Receptors, Fc - metabolism</topic><topic>Receptors, IgE</topic><topic>Solutions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Goldstein, B.</creatorcontrib><creatorcontrib>Posner, R.G.</creatorcontrib><creatorcontrib>Torney, D.C.</creatorcontrib><creatorcontrib>Erickson, J.</creatorcontrib><creatorcontrib>Holowka, D.</creatorcontrib><creatorcontrib>Baird, B.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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>Bacteriology Abstracts (Microbiology B)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biochemistry Abstracts 3</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biophysical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Goldstein, B.</au><au>Posner, R.G.</au><au>Torney, D.C.</au><au>Erickson, J.</au><au>Holowka, D.</au><au>Baird, B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Competition between solution and cell surface receptors for ligand. Dissociation of hapten bound to surface antibody in the presence of solution antibody</atitle><jtitle>Biophysical journal</jtitle><addtitle>Biophys J</addtitle><date>1989-11-01</date><risdate>1989</risdate><volume>56</volume><issue>5</issue><spage>955</spage><epage>966</epage><pages>955-966</pages><issn>0006-3495</issn><eissn>1542-0086</eissn><coden>BIOJAU</coden><abstract>We present a joint theoretical and experimental study on the effects of competition for ligand between receptors in solution and receptors on cell surfaces. We focus on the following experiment. After ligand and cell surface receptors equilibrate, solution receptors are introduced, and the dissociation of surface bound ligand is monitored. We derive theoretical expressions for the dissociation rate and compare with experiment. In a standard dissociation experiment (no solution receptors present) dissociation may be slowed by rebinding, i.e., at high receptor densities a ligand that dissociates from one receptor may rebind to other receptors before separating from the cell. Our theory predicts that rebinding will be prevented when S much greater than N2Kon/(16 pi 2D a4), where S is the free receptor site concentration in solution, N the number of free surface receptor sites per cell, Kon the forward rate constant for ligand-receptor binding in solution, D the diffusion coefficient of the ligand, and a the cell radius. The predicted concentration of solution receptors needed to prevent rebinding is proportional to the square of the cell surface receptor density. The experimental system used in these studies consists of a monovalent ligand, 2,4-dinitrophenyl (DNP)-aminocaproyl-L-tyrosine (DCT), that reversibly binds to a monoclonal anti-DNP immunoglobulin E (IgE). This IgE is both a solution receptor and, when anchored to its high affinity Fc epsilon receptor on rat basophilic leukemia (RBL) cells, a surface receptor. For RBL cells with 6 x 10(5) binding sites per cell, our theory predicts that to prevent DCT rebinding to cell surface IgE during dissociation requires S much greater than 2,400 nM. We show that for S = 200–1,700 nM, the dissociation rate of DCT from surface IgE is substantially slower than from solution IgE where no rebinding occurs. Other predictions are also tested and shown to be consistent with experiment.</abstract><cop>Bethesda, MD</cop><pub>Elsevier Inc</pub><pmid>2532552</pmid><doi>10.1016/S0006-3495(89)82741-9</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antigens, Differentiation, B-Lymphocyte - metabolism Binding, Competitive Biological and medical sciences Cell Line Cell Membrane - immunology Cell receptors Cell structures and functions Fundamental and applied biological sciences. Psychology Haptens Immunoglobulin E - metabolism Kinetics Leukemia, Basophilic, Acute - immunology Leukemia, Experimental - immunology Ligands Mathematics Miscellaneous Models, Theoretical Molecular and cellular biology Rats Receptors, Fc - metabolism Receptors, IgE Solutions |
title | Competition between solution and cell surface receptors for ligand. Dissociation of hapten bound to surface antibody in the presence of solution antibody |
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