Disassembly and reconstitution of yeast 60S ribosomal subunits

Yeast 60S ribosomal subunits have been dissociated by reversible modification with dimethylmaleic anhydride. Treatment with 40 mumol reagent/ml releases 35% of the protein, producing core particles inactive in polyphenylalanine synthesis, which are totally or highly deficient in 17 different protein...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Molecular and cellular biochemistry 1989-03, Vol.86 (1), p.55-63
Hauptverfasser: Nieto, M A, Hernández, F, Palacián, E
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 63
container_issue 1
container_start_page 55
container_title Molecular and cellular biochemistry
container_volume 86
creator Nieto, M A
Hernández, F
Palacián, E
description Yeast 60S ribosomal subunits have been dissociated by reversible modification with dimethylmaleic anhydride. Treatment with 40 mumol reagent/ml releases 35% of the protein, producing core particles inactive in polyphenylalanine synthesis, which are totally or highly deficient in 17 different proteins. This preparation of residual particles recovers 45% of the original activity upon incubation with the released proteins. The reconstituted particles can be isolated by centrifugation without loss of activity, having the protein composition of the original subunits.
doi_str_mv 10.1007/BF00231689
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_79126086</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>79126086</sourcerecordid><originalsourceid>FETCH-LOGICAL-c313t-f72ef724a57cc6fabbb033ad46771d8bc57382e2bc4c0f1badd6342f678907aa3</originalsourceid><addsrcrecordid>eNqF0L1LxEAQBfBFlPM8beyFVBZCdGY3tx-NoKenwoGFWofdzQYiSfbMJEX-eyN3aGkxTPPj8XiMnSNcI4C6uV8DcIFSmwM2x6USaWbQHLI5CIBUo1LH7IToE2DiiDM241JKnZk5u32oyBKFxtVjYtsi6YKPLfVVP_RVbJNYJmOw1CcS3pKucpFiY-uEBje0VU-n7Ki0NYWz_V-wj_Xj--o53bw-vazuNqkXKPq0VDxMl9ml8l6W1jkHQtgik0phoZ2fOmseuPOZhxKdLQopMl5KpQ0oa8WCXe5yt138GgL1eVORD3Vt2xAHypVBLkHLfyEuuTaIYoJXO-i7SNSFMt92VWO7MUfIf1bN_1ad8MU-dXBNKH7pfkbxDSFycW8</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>15289113</pqid></control><display><type>article</type><title>Disassembly and reconstitution of yeast 60S ribosomal subunits</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>Nieto, M A ; Hernández, F ; Palacián, E</creator><creatorcontrib>Nieto, M A ; Hernández, F ; Palacián, E</creatorcontrib><description>Yeast 60S ribosomal subunits have been dissociated by reversible modification with dimethylmaleic anhydride. Treatment with 40 mumol reagent/ml releases 35% of the protein, producing core particles inactive in polyphenylalanine synthesis, which are totally or highly deficient in 17 different proteins. This preparation of residual particles recovers 45% of the original activity upon incubation with the released proteins. The reconstituted particles can be isolated by centrifugation without loss of activity, having the protein composition of the original subunits.</description><identifier>ISSN: 0300-8177</identifier><identifier>EISSN: 1573-4919</identifier><identifier>DOI: 10.1007/BF00231689</identifier><identifier>PMID: 2666849</identifier><language>eng</language><publisher>Netherlands</publisher><subject>Chemical Phenomena ; Chemistry ; Electrophoresis, Polyacrylamide Gel ; Fungal Proteins - isolation &amp; purification ; Fungal Proteins - metabolism ; Hydrogen-Ion Concentration ; Maleic Anhydrides ; Ribosomal Proteins - isolation &amp; purification ; Ribosomal Proteins - metabolism ; RNA, Fungal - analysis ; RNA, Ribosomal - analysis ; Saccharomyces cerevisiae - analysis ; Saccharomyces cerevisiae - metabolism</subject><ispartof>Molecular and cellular biochemistry, 1989-03, Vol.86 (1), p.55-63</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c313t-f72ef724a57cc6fabbb033ad46771d8bc57382e2bc4c0f1badd6342f678907aa3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2666849$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nieto, M A</creatorcontrib><creatorcontrib>Hernández, F</creatorcontrib><creatorcontrib>Palacián, E</creatorcontrib><title>Disassembly and reconstitution of yeast 60S ribosomal subunits</title><title>Molecular and cellular biochemistry</title><addtitle>Mol Cell Biochem</addtitle><description>Yeast 60S ribosomal subunits have been dissociated by reversible modification with dimethylmaleic anhydride. Treatment with 40 mumol reagent/ml releases 35% of the protein, producing core particles inactive in polyphenylalanine synthesis, which are totally or highly deficient in 17 different proteins. This preparation of residual particles recovers 45% of the original activity upon incubation with the released proteins. The reconstituted particles can be isolated by centrifugation without loss of activity, having the protein composition of the original subunits.</description><subject>Chemical Phenomena</subject><subject>Chemistry</subject><subject>Electrophoresis, Polyacrylamide Gel</subject><subject>Fungal Proteins - isolation &amp; purification</subject><subject>Fungal Proteins - metabolism</subject><subject>Hydrogen-Ion Concentration</subject><subject>Maleic Anhydrides</subject><subject>Ribosomal Proteins - isolation &amp; purification</subject><subject>Ribosomal Proteins - metabolism</subject><subject>RNA, Fungal - analysis</subject><subject>RNA, Ribosomal - analysis</subject><subject>Saccharomyces cerevisiae - analysis</subject><subject>Saccharomyces cerevisiae - metabolism</subject><issn>0300-8177</issn><issn>1573-4919</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0L1LxEAQBfBFlPM8beyFVBZCdGY3tx-NoKenwoGFWofdzQYiSfbMJEX-eyN3aGkxTPPj8XiMnSNcI4C6uV8DcIFSmwM2x6USaWbQHLI5CIBUo1LH7IToE2DiiDM241JKnZk5u32oyBKFxtVjYtsi6YKPLfVVP_RVbJNYJmOw1CcS3pKucpFiY-uEBje0VU-n7Ki0NYWz_V-wj_Xj--o53bw-vazuNqkXKPq0VDxMl9ml8l6W1jkHQtgik0phoZ2fOmseuPOZhxKdLQopMl5KpQ0oa8WCXe5yt138GgL1eVORD3Vt2xAHypVBLkHLfyEuuTaIYoJXO-i7SNSFMt92VWO7MUfIf1bN_1ad8MU-dXBNKH7pfkbxDSFycW8</recordid><startdate>19890316</startdate><enddate>19890316</enddate><creator>Nieto, M A</creator><creator>Hernández, F</creator><creator>Palacián, E</creator><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>7TM</scope><scope>M7N</scope><scope>7X8</scope></search><sort><creationdate>19890316</creationdate><title>Disassembly and reconstitution of yeast 60S ribosomal subunits</title><author>Nieto, M A ; Hernández, F ; Palacián, E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c313t-f72ef724a57cc6fabbb033ad46771d8bc57382e2bc4c0f1badd6342f678907aa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Chemical Phenomena</topic><topic>Chemistry</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>Fungal Proteins - isolation &amp; purification</topic><topic>Fungal Proteins - metabolism</topic><topic>Hydrogen-Ion Concentration</topic><topic>Maleic Anhydrides</topic><topic>Ribosomal Proteins - isolation &amp; purification</topic><topic>Ribosomal Proteins - metabolism</topic><topic>RNA, Fungal - analysis</topic><topic>RNA, Ribosomal - analysis</topic><topic>Saccharomyces cerevisiae - analysis</topic><topic>Saccharomyces cerevisiae - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nieto, M A</creatorcontrib><creatorcontrib>Hernández, F</creatorcontrib><creatorcontrib>Palacián, E</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular and cellular biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nieto, M A</au><au>Hernández, F</au><au>Palacián, E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Disassembly and reconstitution of yeast 60S ribosomal subunits</atitle><jtitle>Molecular and cellular biochemistry</jtitle><addtitle>Mol Cell Biochem</addtitle><date>1989-03-16</date><risdate>1989</risdate><volume>86</volume><issue>1</issue><spage>55</spage><epage>63</epage><pages>55-63</pages><issn>0300-8177</issn><eissn>1573-4919</eissn><abstract>Yeast 60S ribosomal subunits have been dissociated by reversible modification with dimethylmaleic anhydride. Treatment with 40 mumol reagent/ml releases 35% of the protein, producing core particles inactive in polyphenylalanine synthesis, which are totally or highly deficient in 17 different proteins. This preparation of residual particles recovers 45% of the original activity upon incubation with the released proteins. The reconstituted particles can be isolated by centrifugation without loss of activity, having the protein composition of the original subunits.</abstract><cop>Netherlands</cop><pmid>2666849</pmid><doi>10.1007/BF00231689</doi><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0300-8177
ispartof Molecular and cellular biochemistry, 1989-03, Vol.86 (1), p.55-63
issn 0300-8177
1573-4919
language eng
recordid cdi_proquest_miscellaneous_79126086
source MEDLINE; SpringerLink Journals - AutoHoldings
subjects Chemical Phenomena
Chemistry
Electrophoresis, Polyacrylamide Gel
Fungal Proteins - isolation & purification
Fungal Proteins - metabolism
Hydrogen-Ion Concentration
Maleic Anhydrides
Ribosomal Proteins - isolation & purification
Ribosomal Proteins - metabolism
RNA, Fungal - analysis
RNA, Ribosomal - analysis
Saccharomyces cerevisiae - analysis
Saccharomyces cerevisiae - metabolism
title Disassembly and reconstitution of yeast 60S ribosomal subunits
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T20%3A46%3A57IST&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=Disassembly%20and%20reconstitution%20of%20yeast%2060S%20ribosomal%20subunits&rft.jtitle=Molecular%20and%20cellular%20biochemistry&rft.au=Nieto,%20M%20A&rft.date=1989-03-16&rft.volume=86&rft.issue=1&rft.spage=55&rft.epage=63&rft.pages=55-63&rft.issn=0300-8177&rft.eissn=1573-4919&rft_id=info:doi/10.1007/BF00231689&rft_dat=%3Cproquest_cross%3E79126086%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=15289113&rft_id=info:pmid/2666849&rfr_iscdi=true