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In vitro glycation of human serum albumin by dihydroxyacetone and dihydroxyacetone phosphate
► Dihydroxyacetone phosphate and dihydroxyacetone are potent glycation agents. ► Glycation of serum albumin is pH, temperature and sugar concentration dependent. ► Dihydroxyacetone is more reactive than dihydroxyacetone phosphate. Amino groups in proteins can non-enzymatically react with reducing su...
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Published in: | Biochemical and biophysical research communications 2012-01, Vol.417 (2), p.817-823 |
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description | ► Dihydroxyacetone phosphate and dihydroxyacetone are potent glycation agents. ► Glycation of serum albumin is pH, temperature and sugar concentration dependent. ► Dihydroxyacetone is more reactive than dihydroxyacetone phosphate.
Amino groups in proteins can non-enzymatically react with reducing sugars to generate a structurally diverse group of compounds referred to as advanced glycation end products (AGEs). The in vivo formation of AGEs contributes to some of the complications of diabetes including atherosclerosis, cataract formation, and renal failure. The formation of AGEs is dependent on both sugar and protein concentrations. Increases in temperature, pH, and exposure time of sugars to the proteins also play a significant role in the rate of AGE formation. This study focuses on the use of a combination of analytical techniques to study the in vitro AGE formation of HSA with dihydroxyacetone phosphate (DHAP), a ketose generated during glycolysis, and its dephosphorylated analog, dihydroxy acetone (DHA), commonly used as a browning reagent in skin tanning preparations. The extent of AGE formation was affected by DHAP and DHA concentrations and by the duration of HSA exposure to these glycating agents. Increases in temperature and pH sped the glycation process and enhanced the formation of the AGEs of HSA. MALDI-TOF mass spectroscopic data provided a reliable result to evaluate the extent of the AGE formation. |
doi_str_mv | 10.1016/j.bbrc.2011.12.043 |
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Amino groups in proteins can non-enzymatically react with reducing sugars to generate a structurally diverse group of compounds referred to as advanced glycation end products (AGEs). The in vivo formation of AGEs contributes to some of the complications of diabetes including atherosclerosis, cataract formation, and renal failure. The formation of AGEs is dependent on both sugar and protein concentrations. Increases in temperature, pH, and exposure time of sugars to the proteins also play a significant role in the rate of AGE formation. This study focuses on the use of a combination of analytical techniques to study the in vitro AGE formation of HSA with dihydroxyacetone phosphate (DHAP), a ketose generated during glycolysis, and its dephosphorylated analog, dihydroxy acetone (DHA), commonly used as a browning reagent in skin tanning preparations. The extent of AGE formation was affected by DHAP and DHA concentrations and by the duration of HSA exposure to these glycating agents. Increases in temperature and pH sped the glycation process and enhanced the formation of the AGEs of HSA. MALDI-TOF mass spectroscopic data provided a reliable result to evaluate the extent of the AGE formation.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1016/j.bbrc.2011.12.043</identifier><identifier>PMID: 22198436</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Advanced glycation end product ; Dihydroxyacetone ; Dihydroxyacetone - chemistry ; Dihydroxyacetone phosphate ; Dihydroxyacetone Phosphate - chemistry ; Glycation End Products, Advanced - chemistry ; Glycosylation ; Human serum albumin ; Humans ; Serum Albumin - chemistry ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</subject><ispartof>Biochemical and biophysical research communications, 2012-01, Vol.417 (2), p.817-823</ispartof><rights>2011 Elsevier Inc.</rights><rights>Copyright © 2011 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c355t-fda3b44b29f92ef1e2858eed7980a14e00edf74bcd794c187786f593c6b81a243</citedby><cites>FETCH-LOGICAL-c355t-fda3b44b29f92ef1e2858eed7980a14e00edf74bcd794c187786f593c6b81a243</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27907,27908</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22198436$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Seneviratne, Champika</creatorcontrib><creatorcontrib>Dombi, G.W.</creatorcontrib><creatorcontrib>Liu, W.</creatorcontrib><creatorcontrib>Dain, J.A.</creatorcontrib><title>In vitro glycation of human serum albumin by dihydroxyacetone and dihydroxyacetone phosphate</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><description>► Dihydroxyacetone phosphate and dihydroxyacetone are potent glycation agents. ► Glycation of serum albumin is pH, temperature and sugar concentration dependent. ► Dihydroxyacetone is more reactive than dihydroxyacetone phosphate.
Amino groups in proteins can non-enzymatically react with reducing sugars to generate a structurally diverse group of compounds referred to as advanced glycation end products (AGEs). The in vivo formation of AGEs contributes to some of the complications of diabetes including atherosclerosis, cataract formation, and renal failure. The formation of AGEs is dependent on both sugar and protein concentrations. Increases in temperature, pH, and exposure time of sugars to the proteins also play a significant role in the rate of AGE formation. This study focuses on the use of a combination of analytical techniques to study the in vitro AGE formation of HSA with dihydroxyacetone phosphate (DHAP), a ketose generated during glycolysis, and its dephosphorylated analog, dihydroxy acetone (DHA), commonly used as a browning reagent in skin tanning preparations. The extent of AGE formation was affected by DHAP and DHA concentrations and by the duration of HSA exposure to these glycating agents. Increases in temperature and pH sped the glycation process and enhanced the formation of the AGEs of HSA. MALDI-TOF mass spectroscopic data provided a reliable result to evaluate the extent of the AGE formation.</description><subject>Advanced glycation end product</subject><subject>Dihydroxyacetone</subject><subject>Dihydroxyacetone - chemistry</subject><subject>Dihydroxyacetone phosphate</subject><subject>Dihydroxyacetone Phosphate - chemistry</subject><subject>Glycation End Products, Advanced - chemistry</subject><subject>Glycosylation</subject><subject>Human serum albumin</subject><subject>Humans</subject><subject>Serum Albumin - chemistry</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNp9kEtL5EAUhQsZ0daZPzALqd2sEutWKukUuBnEFwhuFFwIRT1upqtJUm1VIubfm6ZbNwOuLhy-c-B-hPwGlgOD6nydGxNtzhlADjxnojggC2CSZRyY-EEWjLEq4xKej8lJSms2g6KSR-SYc5C1KKoFebnr6ZsfYqD_2snqwYeehoauxk73NGEcO6pbM3a-p2aizq8mF8P7pC0OoUeqe_d_uFmFtFnpAX-Sw0a3CX_t7yl5ur56vLzN7h9u7i7_3me2KMsha5wujBCGy0ZybAB5XdaIbilrpkEgY-iapTB2ToSFermsq6aUha1MDZqL4pT82e1uYngdMQ2q88li2-oew5iUhKrkUhYwk3xH2hhSitioTfSdjpMCprZS1VptpaqtVAVczVLn0tl-fjQduq_Kp8UZuNgBOD_55jGqZD32Fp2PaAflgv9u_wP7FYoh</recordid><startdate>20120113</startdate><enddate>20120113</enddate><creator>Seneviratne, Champika</creator><creator>Dombi, G.W.</creator><creator>Liu, W.</creator><creator>Dain, J.A.</creator><general>Elsevier Inc</general><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>20120113</creationdate><title>In vitro glycation of human serum albumin by dihydroxyacetone and dihydroxyacetone phosphate</title><author>Seneviratne, Champika ; Dombi, G.W. ; Liu, W. ; Dain, J.A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c355t-fda3b44b29f92ef1e2858eed7980a14e00edf74bcd794c187786f593c6b81a243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Advanced glycation end product</topic><topic>Dihydroxyacetone</topic><topic>Dihydroxyacetone - chemistry</topic><topic>Dihydroxyacetone phosphate</topic><topic>Dihydroxyacetone Phosphate - chemistry</topic><topic>Glycation End Products, Advanced - chemistry</topic><topic>Glycosylation</topic><topic>Human serum albumin</topic><topic>Humans</topic><topic>Serum Albumin - chemistry</topic><topic>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Seneviratne, Champika</creatorcontrib><creatorcontrib>Dombi, G.W.</creatorcontrib><creatorcontrib>Liu, W.</creatorcontrib><creatorcontrib>Dain, J.A.</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><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Seneviratne, Champika</au><au>Dombi, G.W.</au><au>Liu, W.</au><au>Dain, J.A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vitro glycation of human serum albumin by dihydroxyacetone and dihydroxyacetone phosphate</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2012-01-13</date><risdate>2012</risdate><volume>417</volume><issue>2</issue><spage>817</spage><epage>823</epage><pages>817-823</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>► Dihydroxyacetone phosphate and dihydroxyacetone are potent glycation agents. ► Glycation of serum albumin is pH, temperature and sugar concentration dependent. ► Dihydroxyacetone is more reactive than dihydroxyacetone phosphate.
Amino groups in proteins can non-enzymatically react with reducing sugars to generate a structurally diverse group of compounds referred to as advanced glycation end products (AGEs). The in vivo formation of AGEs contributes to some of the complications of diabetes including atherosclerosis, cataract formation, and renal failure. The formation of AGEs is dependent on both sugar and protein concentrations. Increases in temperature, pH, and exposure time of sugars to the proteins also play a significant role in the rate of AGE formation. This study focuses on the use of a combination of analytical techniques to study the in vitro AGE formation of HSA with dihydroxyacetone phosphate (DHAP), a ketose generated during glycolysis, and its dephosphorylated analog, dihydroxy acetone (DHA), commonly used as a browning reagent in skin tanning preparations. The extent of AGE formation was affected by DHAP and DHA concentrations and by the duration of HSA exposure to these glycating agents. Increases in temperature and pH sped the glycation process and enhanced the formation of the AGEs of HSA. MALDI-TOF mass spectroscopic data provided a reliable result to evaluate the extent of the AGE formation.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>22198436</pmid><doi>10.1016/j.bbrc.2011.12.043</doi><tpages>7</tpages></addata></record> |
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subjects | Advanced glycation end product Dihydroxyacetone Dihydroxyacetone - chemistry Dihydroxyacetone phosphate Dihydroxyacetone Phosphate - chemistry Glycation End Products, Advanced - chemistry Glycosylation Human serum albumin Humans Serum Albumin - chemistry Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization |
title | In vitro glycation of human serum albumin by dihydroxyacetone and dihydroxyacetone phosphate |
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