Lysosomal sulphate transport is dependent upon sulphydryl groups
Using thiol blocking agents, we examined the role of sulphydryl groups for function of the lysosomal sulphate transport system. Monothiol binding reagents, p-hydroxymercuribenzoic acid (p-HMB) and p-chloromercuribenzene sulphonic acid (p-CMBS), dithiol binding reagents such as CuCl2, the alkylating...
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Veröffentlicht in: | Biochemical journal 1998-03, Vol.330 ( Pt 2) (2), p.713-717 |
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description | Using thiol blocking agents, we examined the role of sulphydryl groups for function of the lysosomal sulphate transport system. Monothiol binding reagents, p-hydroxymercuribenzoic acid (p-HMB) and p-chloromercuribenzene sulphonic acid (p-CMBS), dithiol binding reagents such as CuCl2, the alkylating agent, N-ethylmaleimide (NEM), and NADH all inhibited lysosomal sulphate transport. The inhibitory effects of NEM and Cu2+ were not additive, suggesting that they both act upon the same critical sulphydryl group(s). Unlike the case for NEM, the inhibitory effects of Cu2+ were reversed by the reducing agent, dithiothreitol. Exposure to NEM resulted in a seven-fold increase in Km to 867 microM versus a control value of 126 microM and a modest decrease in Vmax to 99 pmolperunit beta-hexosaminidase per 30 s versus a control value of 129 pmolperunit beta-hexosaminidase per 30 s. Similar although somewhat less dramatic results were obtained using Cu2+ with an increase of Km to 448 microM and a Vmax of 77 pmolperunit beta-hexosaminidase per 30 s. The sulphate transport activity of detergent solubilized lysosomal membranes could be bound to a p-chloromercuribenzoic acid (p-CMB)-Sepharose sulphydryl affinity resin and eluted with mercaptoethanol. Sulphydryl groups thus appear to play a role in sulphate transport through effects on substrate affinity. Sulphydryl-binding appears to be a strategy that may be useful for purification of the transporter. |
doi_str_mv | 10.1042/bj3300713 |
format | Article |
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Monothiol binding reagents, p-hydroxymercuribenzoic acid (p-HMB) and p-chloromercuribenzene sulphonic acid (p-CMBS), dithiol binding reagents such as CuCl2, the alkylating agent, N-ethylmaleimide (NEM), and NADH all inhibited lysosomal sulphate transport. The inhibitory effects of NEM and Cu2+ were not additive, suggesting that they both act upon the same critical sulphydryl group(s). Unlike the case for NEM, the inhibitory effects of Cu2+ were reversed by the reducing agent, dithiothreitol. Exposure to NEM resulted in a seven-fold increase in Km to 867 microM versus a control value of 126 microM and a modest decrease in Vmax to 99 pmolperunit beta-hexosaminidase per 30 s versus a control value of 129 pmolperunit beta-hexosaminidase per 30 s. Similar although somewhat less dramatic results were obtained using Cu2+ with an increase of Km to 448 microM and a Vmax of 77 pmolperunit beta-hexosaminidase per 30 s. The sulphate transport activity of detergent solubilized lysosomal membranes could be bound to a p-chloromercuribenzoic acid (p-CMB)-Sepharose sulphydryl affinity resin and eluted with mercaptoethanol. Sulphydryl groups thus appear to play a role in sulphate transport through effects on substrate affinity. Sulphydryl-binding appears to be a strategy that may be useful for purification of the transporter.</description><identifier>ISSN: 0264-6021</identifier><identifier>EISSN: 1470-8728</identifier><identifier>DOI: 10.1042/bj3300713</identifier><identifier>PMID: 9480880</identifier><language>eng</language><publisher>England</publisher><subject>Animals ; Biological Transport - drug effects ; Copper - metabolism ; Dithiothreitol - pharmacology ; Ethylmaleimide - pharmacology ; Female ; Kinetics ; Lysosomes - drug effects ; Lysosomes - metabolism ; Rats ; Rats, Sprague-Dawley ; Sulfates - metabolism ; Sulfhydryl Compounds - metabolism ; Sulfhydryl Reagents - pharmacology</subject><ispartof>Biochemical journal, 1998-03, Vol.330 ( Pt 2) (2), p.713-717</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c370t-54ebd73a561a01acddd14b9ea143a265e4e6980cc5a61ea20b5441b438cb9ee73</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/PMC1219195/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1219195/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9480880$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chou, H F</creatorcontrib><creatorcontrib>Passage, M</creatorcontrib><creatorcontrib>Jonas, A J</creatorcontrib><title>Lysosomal sulphate transport is dependent upon sulphydryl groups</title><title>Biochemical journal</title><addtitle>Biochem J</addtitle><description>Using thiol blocking agents, we examined the role of sulphydryl groups for function of the lysosomal sulphate transport system. Monothiol binding reagents, p-hydroxymercuribenzoic acid (p-HMB) and p-chloromercuribenzene sulphonic acid (p-CMBS), dithiol binding reagents such as CuCl2, the alkylating agent, N-ethylmaleimide (NEM), and NADH all inhibited lysosomal sulphate transport. The inhibitory effects of NEM and Cu2+ were not additive, suggesting that they both act upon the same critical sulphydryl group(s). Unlike the case for NEM, the inhibitory effects of Cu2+ were reversed by the reducing agent, dithiothreitol. Exposure to NEM resulted in a seven-fold increase in Km to 867 microM versus a control value of 126 microM and a modest decrease in Vmax to 99 pmolperunit beta-hexosaminidase per 30 s versus a control value of 129 pmolperunit beta-hexosaminidase per 30 s. Similar although somewhat less dramatic results were obtained using Cu2+ with an increase of Km to 448 microM and a Vmax of 77 pmolperunit beta-hexosaminidase per 30 s. The sulphate transport activity of detergent solubilized lysosomal membranes could be bound to a p-chloromercuribenzoic acid (p-CMB)-Sepharose sulphydryl affinity resin and eluted with mercaptoethanol. Sulphydryl groups thus appear to play a role in sulphate transport through effects on substrate affinity. Sulphydryl-binding appears to be a strategy that may be useful for purification of the transporter.</description><subject>Animals</subject><subject>Biological Transport - drug effects</subject><subject>Copper - metabolism</subject><subject>Dithiothreitol - pharmacology</subject><subject>Ethylmaleimide - pharmacology</subject><subject>Female</subject><subject>Kinetics</subject><subject>Lysosomes - drug effects</subject><subject>Lysosomes - metabolism</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Sulfates - metabolism</subject><subject>Sulfhydryl Compounds - metabolism</subject><subject>Sulfhydryl Reagents - pharmacology</subject><issn>0264-6021</issn><issn>1470-8728</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkE1Lw0AURQdRaq0u_AFCVoKL6HuZSSbZiFL8goIbXQ-Tmdc2Jc3EmUTIvzfSUnT1Fu9w7uUydolwiyCSu3LDOYBEfsSmKCTEuUzyYzaFJBNxBgmesrMQNgAoQMCETQqRQ57DlD0shuCC2-o6Cn3drnVHUed1E1rnu6gKkaWWGktNF_Wta3bQYP1QRyvv-jacs5OlrgNd7O-MfT4_fcxf48X7y9v8cREbLqGLU0GllVynGWpAbay1KMqCNAqukywlQVmRgzGpzpB0AmUqBJaC52akSPIZu995277ckjVjI69r1fpqq_2gnK7U_09TrdXKfStMsMAiHQXXe4F3Xz2FTm2rYKiudUOuD0oWEjErcARvdqDxLgRPy0MIgvqdWx3mHtmrv60O5H5f_gNHkXzq</recordid><startdate>19980301</startdate><enddate>19980301</enddate><creator>Chou, H F</creator><creator>Passage, M</creator><creator>Jonas, A J</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>19980301</creationdate><title>Lysosomal sulphate transport is dependent upon sulphydryl groups</title><author>Chou, H F ; Passage, M ; Jonas, A J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c370t-54ebd73a561a01acddd14b9ea143a265e4e6980cc5a61ea20b5441b438cb9ee73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Biological Transport - drug effects</topic><topic>Copper - metabolism</topic><topic>Dithiothreitol - pharmacology</topic><topic>Ethylmaleimide - pharmacology</topic><topic>Female</topic><topic>Kinetics</topic><topic>Lysosomes - drug effects</topic><topic>Lysosomes - metabolism</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Sulfates - metabolism</topic><topic>Sulfhydryl Compounds - metabolism</topic><topic>Sulfhydryl Reagents - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chou, H F</creatorcontrib><creatorcontrib>Passage, M</creatorcontrib><creatorcontrib>Jonas, A J</creatorcontrib><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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biochemical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chou, H F</au><au>Passage, M</au><au>Jonas, A J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lysosomal sulphate transport is dependent upon sulphydryl groups</atitle><jtitle>Biochemical journal</jtitle><addtitle>Biochem J</addtitle><date>1998-03-01</date><risdate>1998</risdate><volume>330 ( Pt 2)</volume><issue>2</issue><spage>713</spage><epage>717</epage><pages>713-717</pages><issn>0264-6021</issn><eissn>1470-8728</eissn><abstract>Using thiol blocking agents, we examined the role of sulphydryl groups for function of the lysosomal sulphate transport system. Monothiol binding reagents, p-hydroxymercuribenzoic acid (p-HMB) and p-chloromercuribenzene sulphonic acid (p-CMBS), dithiol binding reagents such as CuCl2, the alkylating agent, N-ethylmaleimide (NEM), and NADH all inhibited lysosomal sulphate transport. The inhibitory effects of NEM and Cu2+ were not additive, suggesting that they both act upon the same critical sulphydryl group(s). Unlike the case for NEM, the inhibitory effects of Cu2+ were reversed by the reducing agent, dithiothreitol. Exposure to NEM resulted in a seven-fold increase in Km to 867 microM versus a control value of 126 microM and a modest decrease in Vmax to 99 pmolperunit beta-hexosaminidase per 30 s versus a control value of 129 pmolperunit beta-hexosaminidase per 30 s. Similar although somewhat less dramatic results were obtained using Cu2+ with an increase of Km to 448 microM and a Vmax of 77 pmolperunit beta-hexosaminidase per 30 s. The sulphate transport activity of detergent solubilized lysosomal membranes could be bound to a p-chloromercuribenzoic acid (p-CMB)-Sepharose sulphydryl affinity resin and eluted with mercaptoethanol. Sulphydryl groups thus appear to play a role in sulphate transport through effects on substrate affinity. Sulphydryl-binding appears to be a strategy that may be useful for purification of the transporter.</abstract><cop>England</cop><pmid>9480880</pmid><doi>10.1042/bj3300713</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Alma/SFX Local Collection |
subjects | Animals Biological Transport - drug effects Copper - metabolism Dithiothreitol - pharmacology Ethylmaleimide - pharmacology Female Kinetics Lysosomes - drug effects Lysosomes - metabolism Rats Rats, Sprague-Dawley Sulfates - metabolism Sulfhydryl Compounds - metabolism Sulfhydryl Reagents - pharmacology |
title | Lysosomal sulphate transport is dependent upon sulphydryl groups |
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