Pressure effects on the binding of vanadate to the sarcoplasmic reticulum calcium‐transport enzyme
The effect which hydrostatic pressure exerts on the binding of vanadate to the calcium‐transport enzyme was determined. The recent unavailability of radioactive vanadate prevented direct measurements of vanadate binding. The vanadate‐free enzyme fraction was instead monitored by phosphorylating it w...
Gespeichert in:
Veröffentlicht in: | European journal of biochemistry 1991-10, Vol.201 (1), p.265-271 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 271 |
---|---|
container_issue | 1 |
container_start_page | 265 |
container_title | European journal of biochemistry |
container_volume | 201 |
creator | RONZANI, Nelly STEPHAN, Lore HASSELBACH, Wilhelm |
description | The effect which hydrostatic pressure exerts on the binding of vanadate to the calcium‐transport enzyme was determined. The recent unavailability of radioactive vanadate prevented direct measurements of vanadate binding.
The vanadate‐free enzyme fraction was instead monitored by phosphorylating it with ATP according to Medda and Hasselbach [Medda, P. & Hasselbach, W. (1983) Eur. J. Biochem. 137, 7–14]. Vanadate binding is reduced with rising pressure at first markedly and subsequently, above 30 MPa, relatively little. The biphasic pressure‐binding relationship was analysed by applying a biexponential fitting procedure to the experimental data. The biphasicity of the pressure‐binding relationship indicates that the description of vanadate binding requires at least a two‐step reaction sequence. The volume increments which predominate at lower pressure values, range from 200–400 ml · mol−1 depending on the composition of the reaction medium containig 5 μM and 20 μM vanadate and no or 15% (by vol.) Me2SO. The binding volumes deduced for the higher pressure range amount to 20–40 ml · mol−1. Vanadate binding is reduced in the presence of 30 μM calcium, and simultaneously both binding volumes are diminished by 100 ml · mol−1 and 20 ml · mol−1 for the low and high pressure values, respectively, as one can expect for mutual interactions between the two ligands of the transport enzyme. |
doi_str_mv | 10.1111/j.1432-1033.1991.tb16283.x |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_72131733</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>16144007</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4305-adcf0fefd2df897dbfd07cbe89e0954f08647e925174af5708b482228e7f49253</originalsourceid><addsrcrecordid>eNqVkd1qFDEYhoModa1eghBEPJsxfzNJPBEtrQqFFtTjkEm-aJb5WZOM7fbIS_AaeyXOuks9LOYkkPf5kvC8CL2gpKbLer2uqeCsooTzmmpN69LRlileXz9Aq7voIVoRQkXFdNM-Rk9yXhNCWt3KI3REFedUixXylwlynhNgCAFcyXgacfkOuIujj-M3PAX8047W2wK4TH-jbJObNr3NQ3Q4QYlu7ucBO9u7OA-3v36XZMe8mVLBMN5sB3iKHgXbZ3h22I_R17PTLycfq_OLD59O3p1XTnDSVNa7QAIEz3xQWvoueCJdB0oD0Y0IRLVCgmYNlcKGRhLVCcUYUyCDWI75MXq1v3eTph8z5GKGmB30vR1hmrORjHIqOb8XpC0VghC5gG_2oEtTzgmC2aQ42LQ1lJhdF2ZtdsLNTrjZdWEOXZjrZfj54ZW5G8D_G93LX_KXh9zmRV5YrLmY77CGNlxotWBv99hV7GH7Hx8wZ6fvP7O24X8AZ0yorA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>16144007</pqid></control><display><type>article</type><title>Pressure effects on the binding of vanadate to the sarcoplasmic reticulum calcium‐transport enzyme</title><source>MEDLINE</source><source>Alma/SFX Local Collection</source><creator>RONZANI, Nelly ; STEPHAN, Lore ; HASSELBACH, Wilhelm</creator><creatorcontrib>RONZANI, Nelly ; STEPHAN, Lore ; HASSELBACH, Wilhelm</creatorcontrib><description>The effect which hydrostatic pressure exerts on the binding of vanadate to the calcium‐transport enzyme was determined. The recent unavailability of radioactive vanadate prevented direct measurements of vanadate binding.
The vanadate‐free enzyme fraction was instead monitored by phosphorylating it with ATP according to Medda and Hasselbach [Medda, P. & Hasselbach, W. (1983) Eur. J. Biochem. 137, 7–14]. Vanadate binding is reduced with rising pressure at first markedly and subsequently, above 30 MPa, relatively little. The biphasic pressure‐binding relationship was analysed by applying a biexponential fitting procedure to the experimental data. The biphasicity of the pressure‐binding relationship indicates that the description of vanadate binding requires at least a two‐step reaction sequence. The volume increments which predominate at lower pressure values, range from 200–400 ml · mol−1 depending on the composition of the reaction medium containig 5 μM and 20 μM vanadate and no or 15% (by vol.) Me2SO. The binding volumes deduced for the higher pressure range amount to 20–40 ml · mol−1. Vanadate binding is reduced in the presence of 30 μM calcium, and simultaneously both binding volumes are diminished by 100 ml · mol−1 and 20 ml · mol−1 for the low and high pressure values, respectively, as one can expect for mutual interactions between the two ligands of the transport enzyme.</description><identifier>ISSN: 0014-2956</identifier><identifier>EISSN: 1432-1033</identifier><identifier>DOI: 10.1111/j.1432-1033.1991.tb16283.x</identifier><identifier>PMID: 1833194</identifier><identifier>CODEN: EJBCAI</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adenosine Triphosphate - metabolism ; Animals ; Biological and medical sciences ; Ca super(2+)-transporting ATPase ; Calcium - pharmacology ; Calcium-Transporting ATPases - metabolism ; Cell physiology ; Effects of physical and chemical agents ; Fundamental and applied biological sciences. Psychology ; Molecular and cellular biology ; Muscles - enzymology ; Phosphoproteins - metabolism ; Phosphorylation ; Pressure ; Rabbits ; Sarcoplasmic Reticulum - enzymology ; vanadate ; Vanadates - metabolism</subject><ispartof>European journal of biochemistry, 1991-10, Vol.201 (1), p.265-271</ispartof><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4305-adcf0fefd2df897dbfd07cbe89e0954f08647e925174af5708b482228e7f49253</citedby><cites>FETCH-LOGICAL-c4305-adcf0fefd2df897dbfd07cbe89e0954f08647e925174af5708b482228e7f49253</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5153498$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1833194$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>RONZANI, Nelly</creatorcontrib><creatorcontrib>STEPHAN, Lore</creatorcontrib><creatorcontrib>HASSELBACH, Wilhelm</creatorcontrib><title>Pressure effects on the binding of vanadate to the sarcoplasmic reticulum calcium‐transport enzyme</title><title>European journal of biochemistry</title><addtitle>Eur J Biochem</addtitle><description>The effect which hydrostatic pressure exerts on the binding of vanadate to the calcium‐transport enzyme was determined. The recent unavailability of radioactive vanadate prevented direct measurements of vanadate binding.
The vanadate‐free enzyme fraction was instead monitored by phosphorylating it with ATP according to Medda and Hasselbach [Medda, P. & Hasselbach, W. (1983) Eur. J. Biochem. 137, 7–14]. Vanadate binding is reduced with rising pressure at first markedly and subsequently, above 30 MPa, relatively little. The biphasic pressure‐binding relationship was analysed by applying a biexponential fitting procedure to the experimental data. The biphasicity of the pressure‐binding relationship indicates that the description of vanadate binding requires at least a two‐step reaction sequence. The volume increments which predominate at lower pressure values, range from 200–400 ml · mol−1 depending on the composition of the reaction medium containig 5 μM and 20 μM vanadate and no or 15% (by vol.) Me2SO. The binding volumes deduced for the higher pressure range amount to 20–40 ml · mol−1. Vanadate binding is reduced in the presence of 30 μM calcium, and simultaneously both binding volumes are diminished by 100 ml · mol−1 and 20 ml · mol−1 for the low and high pressure values, respectively, as one can expect for mutual interactions between the two ligands of the transport enzyme.</description><subject>Adenosine Triphosphate - metabolism</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Ca super(2+)-transporting ATPase</subject><subject>Calcium - pharmacology</subject><subject>Calcium-Transporting ATPases - metabolism</subject><subject>Cell physiology</subject><subject>Effects of physical and chemical agents</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Molecular and cellular biology</subject><subject>Muscles - enzymology</subject><subject>Phosphoproteins - metabolism</subject><subject>Phosphorylation</subject><subject>Pressure</subject><subject>Rabbits</subject><subject>Sarcoplasmic Reticulum - enzymology</subject><subject>vanadate</subject><subject>Vanadates - metabolism</subject><issn>0014-2956</issn><issn>1432-1033</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkd1qFDEYhoModa1eghBEPJsxfzNJPBEtrQqFFtTjkEm-aJb5WZOM7fbIS_AaeyXOuks9LOYkkPf5kvC8CL2gpKbLer2uqeCsooTzmmpN69LRlileXz9Aq7voIVoRQkXFdNM-Rk9yXhNCWt3KI3REFedUixXylwlynhNgCAFcyXgacfkOuIujj-M3PAX8047W2wK4TH-jbJObNr3NQ3Q4QYlu7ucBO9u7OA-3v36XZMe8mVLBMN5sB3iKHgXbZ3h22I_R17PTLycfq_OLD59O3p1XTnDSVNa7QAIEz3xQWvoueCJdB0oD0Y0IRLVCgmYNlcKGRhLVCcUYUyCDWI75MXq1v3eTph8z5GKGmB30vR1hmrORjHIqOb8XpC0VghC5gG_2oEtTzgmC2aQ42LQ1lJhdF2ZtdsLNTrjZdWEOXZjrZfj54ZW5G8D_G93LX_KXh9zmRV5YrLmY77CGNlxotWBv99hV7GH7Hx8wZ6fvP7O24X8AZ0yorA</recordid><startdate>199110</startdate><enddate>199110</enddate><creator>RONZANI, Nelly</creator><creator>STEPHAN, Lore</creator><creator>HASSELBACH, Wilhelm</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><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>7QP</scope><scope>8FD</scope><scope>FR3</scope><scope>M7Z</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>199110</creationdate><title>Pressure effects on the binding of vanadate to the sarcoplasmic reticulum calcium‐transport enzyme</title><author>RONZANI, Nelly ; STEPHAN, Lore ; HASSELBACH, Wilhelm</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4305-adcf0fefd2df897dbfd07cbe89e0954f08647e925174af5708b482228e7f49253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Adenosine Triphosphate - metabolism</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Ca super(2+)-transporting ATPase</topic><topic>Calcium - pharmacology</topic><topic>Calcium-Transporting ATPases - metabolism</topic><topic>Cell physiology</topic><topic>Effects of physical and chemical agents</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Molecular and cellular biology</topic><topic>Muscles - enzymology</topic><topic>Phosphoproteins - metabolism</topic><topic>Phosphorylation</topic><topic>Pressure</topic><topic>Rabbits</topic><topic>Sarcoplasmic Reticulum - enzymology</topic><topic>vanadate</topic><topic>Vanadates - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>RONZANI, Nelly</creatorcontrib><creatorcontrib>STEPHAN, Lore</creatorcontrib><creatorcontrib>HASSELBACH, Wilhelm</creatorcontrib><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>Calcium & Calcified Tissue Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>RONZANI, Nelly</au><au>STEPHAN, Lore</au><au>HASSELBACH, Wilhelm</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pressure effects on the binding of vanadate to the sarcoplasmic reticulum calcium‐transport enzyme</atitle><jtitle>European journal of biochemistry</jtitle><addtitle>Eur J Biochem</addtitle><date>1991-10</date><risdate>1991</risdate><volume>201</volume><issue>1</issue><spage>265</spage><epage>271</epage><pages>265-271</pages><issn>0014-2956</issn><eissn>1432-1033</eissn><coden>EJBCAI</coden><abstract>The effect which hydrostatic pressure exerts on the binding of vanadate to the calcium‐transport enzyme was determined. The recent unavailability of radioactive vanadate prevented direct measurements of vanadate binding.
The vanadate‐free enzyme fraction was instead monitored by phosphorylating it with ATP according to Medda and Hasselbach [Medda, P. & Hasselbach, W. (1983) Eur. J. Biochem. 137, 7–14]. Vanadate binding is reduced with rising pressure at first markedly and subsequently, above 30 MPa, relatively little. The biphasic pressure‐binding relationship was analysed by applying a biexponential fitting procedure to the experimental data. The biphasicity of the pressure‐binding relationship indicates that the description of vanadate binding requires at least a two‐step reaction sequence. The volume increments which predominate at lower pressure values, range from 200–400 ml · mol−1 depending on the composition of the reaction medium containig 5 μM and 20 μM vanadate and no or 15% (by vol.) Me2SO. The binding volumes deduced for the higher pressure range amount to 20–40 ml · mol−1. Vanadate binding is reduced in the presence of 30 μM calcium, and simultaneously both binding volumes are diminished by 100 ml · mol−1 and 20 ml · mol−1 for the low and high pressure values, respectively, as one can expect for mutual interactions between the two ligands of the transport enzyme.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>1833194</pmid><doi>10.1111/j.1432-1033.1991.tb16283.x</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0014-2956 |
ispartof | European journal of biochemistry, 1991-10, Vol.201 (1), p.265-271 |
issn | 0014-2956 1432-1033 |
language | eng |
recordid | cdi_proquest_miscellaneous_72131733 |
source | MEDLINE; Alma/SFX Local Collection |
subjects | Adenosine Triphosphate - metabolism Animals Biological and medical sciences Ca super(2+)-transporting ATPase Calcium - pharmacology Calcium-Transporting ATPases - metabolism Cell physiology Effects of physical and chemical agents Fundamental and applied biological sciences. Psychology Molecular and cellular biology Muscles - enzymology Phosphoproteins - metabolism Phosphorylation Pressure Rabbits Sarcoplasmic Reticulum - enzymology vanadate Vanadates - metabolism |
title | Pressure effects on the binding of vanadate to the sarcoplasmic reticulum calcium‐transport enzyme |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T02%3A11%3A16IST&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=Pressure%20effects%20on%20the%20binding%20of%20vanadate%20to%20the%20sarcoplasmic%20reticulum%20calcium%E2%80%90transport%20enzyme&rft.jtitle=European%20journal%20of%20biochemistry&rft.au=RONZANI,%20Nelly&rft.date=1991-10&rft.volume=201&rft.issue=1&rft.spage=265&rft.epage=271&rft.pages=265-271&rft.issn=0014-2956&rft.eissn=1432-1033&rft.coden=EJBCAI&rft_id=info:doi/10.1111/j.1432-1033.1991.tb16283.x&rft_dat=%3Cproquest_cross%3E16144007%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=16144007&rft_id=info:pmid/1833194&rfr_iscdi=true |