Mixed-mode hydrophilic interaction/cation-exchange chromatography: Separation of complex mixtures of peptides of varying charge and hydrophobicity
Mixed-mode hydrophilic interaction/cation-exchange chromatography (HILIC/CEX) was applied to the separation of two mixtures of synthetic peptide standards: (i) a 27-peptide mixture containing three groups of peptides (each group containing nine peptides of the same net charge of +1, +2 or +3), where...
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Veröffentlicht in: | Journal of separation science 2008-05, Vol.31 (9), p.1573-1584 |
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description | Mixed-mode hydrophilic interaction/cation-exchange chromatography (HILIC/CEX) was applied to the separation of two mixtures of synthetic peptide standards: (i) a 27-peptide mixture containing three groups of peptides (each group containing nine peptides of the same net charge of +1, +2 or +3), where the hydrophilicity/hydrophobicity of adjacent peptides within the groups varied only subtly (generally by only a single carbon atom); and (ii) peptide pairs with the same composition but different sequences, where the sole difference between the peptides was the position of a single amino acid substitution. HILIC/CEX is essentially CEX chromatography in the presence of high levels of organic modifier (generally ACN). The present study demonstrated the dramatic effect of increasing ACN concentration (optimum levels of 60-80%, depending on the application) on the separation of both mixtures of peptides. The greater the charge on the peptides, the better the separation achievable by HILIC/CEX. In addition, HILIC/CEX separation of both the peptide mixtures used in the present study was shown to be superior to that of the more commonly applied RP-HPLC mode. Our results highlight again the efficacy of HILIC/CEX as a peptide separation mode in its own right as well as an excellent complement to RP-HPLC. |
doi_str_mv | 10.1002/jssc.200700619 |
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HILIC/CEX is essentially CEX chromatography in the presence of high levels of organic modifier (generally ACN). The present study demonstrated the dramatic effect of increasing ACN concentration (optimum levels of 60-80%, depending on the application) on the separation of both mixtures of peptides. The greater the charge on the peptides, the better the separation achievable by HILIC/CEX. In addition, HILIC/CEX separation of both the peptide mixtures used in the present study was shown to be superior to that of the more commonly applied RP-HPLC mode. Our results highlight again the efficacy of HILIC/CEX as a peptide separation mode in its own right as well as an excellent complement to RP-HPLC.</description><identifier>ISSN: 1615-9306</identifier><identifier>EISSN: 1615-9314</identifier><identifier>DOI: 10.1002/jssc.200700619</identifier><identifier>PMID: 18461566</identifier><language>eng</language><publisher>Weinheim: Wiley-VCH Verlag</publisher><subject>Amino Acid Sequence ; Cation-exchange chromatography ; Chromatography, High Pressure Liquid - methods ; Chromatography, Ion Exchange - methods ; Chromatography, Ion Exchange - standards ; Chromatography, Liquid - methods ; Chromatography, Liquid - standards ; Electrochemistry ; Hydrophilic interaction ; Hydrophobic and Hydrophilic Interactions ; Indicators and Reagents ; Ion-interaction capillary zone electrophoresis ; Oligopeptides - chemistry ; Oligopeptides - isolation & purification ; Oligopeptides - standards ; Peptides ; Reference Standards ; Reversed-phase high-performance liquid chromatography ; Solvents</subject><ispartof>Journal of separation science, 2008-05, Vol.31 (9), p.1573-1584</ispartof><rights>Copyright © 2008 WILEY‐VCH Verlag GmbH & Co. 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KGaA, Weinheim 2008</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5979-7b27a6b4f4d1d5005120964b9a27be5d9b04ed010d7efc9a72ce5b2b79a97aed3</citedby><cites>FETCH-LOGICAL-c5979-7b27a6b4f4d1d5005120964b9a27be5d9b04ed010d7efc9a72ce5b2b79a97aed3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjssc.200700619$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjssc.200700619$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18461566$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mant, Colin T</creatorcontrib><creatorcontrib>Hodges, Robert S</creatorcontrib><title>Mixed-mode hydrophilic interaction/cation-exchange chromatography: Separation of complex mixtures of peptides of varying charge and hydrophobicity</title><title>Journal of separation science</title><addtitle>J. Sep. Science</addtitle><description>Mixed-mode hydrophilic interaction/cation-exchange chromatography (HILIC/CEX) was applied to the separation of two mixtures of synthetic peptide standards: (i) a 27-peptide mixture containing three groups of peptides (each group containing nine peptides of the same net charge of +1, +2 or +3), where the hydrophilicity/hydrophobicity of adjacent peptides within the groups varied only subtly (generally by only a single carbon atom); and (ii) peptide pairs with the same composition but different sequences, where the sole difference between the peptides was the position of a single amino acid substitution. HILIC/CEX is essentially CEX chromatography in the presence of high levels of organic modifier (generally ACN). The present study demonstrated the dramatic effect of increasing ACN concentration (optimum levels of 60-80%, depending on the application) on the separation of both mixtures of peptides. The greater the charge on the peptides, the better the separation achievable by HILIC/CEX. In addition, HILIC/CEX separation of both the peptide mixtures used in the present study was shown to be superior to that of the more commonly applied RP-HPLC mode. Our results highlight again the efficacy of HILIC/CEX as a peptide separation mode in its own right as well as an excellent complement to RP-HPLC.</description><subject>Amino Acid Sequence</subject><subject>Cation-exchange chromatography</subject><subject>Chromatography, High Pressure Liquid - methods</subject><subject>Chromatography, Ion Exchange - methods</subject><subject>Chromatography, Ion Exchange - standards</subject><subject>Chromatography, Liquid - methods</subject><subject>Chromatography, Liquid - standards</subject><subject>Electrochemistry</subject><subject>Hydrophilic interaction</subject><subject>Hydrophobic and Hydrophilic Interactions</subject><subject>Indicators and Reagents</subject><subject>Ion-interaction capillary zone electrophoresis</subject><subject>Oligopeptides - chemistry</subject><subject>Oligopeptides - isolation & purification</subject><subject>Oligopeptides - standards</subject><subject>Peptides</subject><subject>Reference Standards</subject><subject>Reversed-phase high-performance liquid chromatography</subject><subject>Solvents</subject><issn>1615-9306</issn><issn>1615-9314</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFu1DAQhiMEoqVw5Qg5cct2bCf2mgNStYICWgrSUpWb5diTjUsSBztbdl-DJyZLylJOPXnk-ebzWH-SPCcwIwD09DpGM6MAAoAT-SA5JpwUmWQkf3iogR8lT2K8BiBiLuFxckTm-dji_Dj59clt0Watt5jWOxt8X7vGmdR1AwZtBue7U6P3R4ZbU-tujampg2_14NdB9_XudbrCXoc_TOqr1Pi2b3Cbtm47bALG_V2P_eDsVN_osHPderToMMp0Z_8-7Etn3LB7mjyqdBPx2e15kly-e_t18T5bfj7_sDhbZqaQQmaipELzMq9yS2wBUBAKkuel1FSUWFhZQo4WCFiBlZFaUINFSUshtRQaLTtJ3kzeflO2aA12Q9CN6oNrxxWV10793-lcrdb-RlFR8Hyej4JXt4Lgf2wwDqp10WDT6A79JipB-LhSzu8FGWNzIpkcwdkEmuBjDFgdtiGg9nmrfd7qkPc48OLuH_7htwGPgJyAn67B3T069XG1WtyVZ9OsiwNuD7M6fFdcMFGoq4tzRdlyARdfvqmrkX858ZX2Sq-Di-pyRYEwAAlMCMp-A1o11fw</recordid><startdate>200805</startdate><enddate>200805</enddate><creator>Mant, Colin T</creator><creator>Hodges, Robert S</creator><general>Wiley-VCH Verlag</general><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>FBQ</scope><scope>BSCLL</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>7U5</scope><scope>8FD</scope><scope>L7M</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>200805</creationdate><title>Mixed-mode hydrophilic interaction/cation-exchange chromatography: Separation of complex mixtures of peptides of varying charge and hydrophobicity</title><author>Mant, Colin T ; Hodges, Robert S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5979-7b27a6b4f4d1d5005120964b9a27be5d9b04ed010d7efc9a72ce5b2b79a97aed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Amino Acid Sequence</topic><topic>Cation-exchange chromatography</topic><topic>Chromatography, High Pressure Liquid - methods</topic><topic>Chromatography, Ion Exchange - methods</topic><topic>Chromatography, Ion Exchange - standards</topic><topic>Chromatography, Liquid - methods</topic><topic>Chromatography, Liquid - standards</topic><topic>Electrochemistry</topic><topic>Hydrophilic interaction</topic><topic>Hydrophobic and Hydrophilic Interactions</topic><topic>Indicators and Reagents</topic><topic>Ion-interaction capillary zone electrophoresis</topic><topic>Oligopeptides - chemistry</topic><topic>Oligopeptides - isolation & purification</topic><topic>Oligopeptides - standards</topic><topic>Peptides</topic><topic>Reference Standards</topic><topic>Reversed-phase high-performance liquid chromatography</topic><topic>Solvents</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mant, Colin T</creatorcontrib><creatorcontrib>Hodges, Robert S</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of separation science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mant, Colin T</au><au>Hodges, Robert S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mixed-mode hydrophilic interaction/cation-exchange chromatography: Separation of complex mixtures of peptides of varying charge and hydrophobicity</atitle><jtitle>Journal of separation science</jtitle><addtitle>J. Sep. Science</addtitle><date>2008-05</date><risdate>2008</risdate><volume>31</volume><issue>9</issue><spage>1573</spage><epage>1584</epage><pages>1573-1584</pages><issn>1615-9306</issn><eissn>1615-9314</eissn><abstract>Mixed-mode hydrophilic interaction/cation-exchange chromatography (HILIC/CEX) was applied to the separation of two mixtures of synthetic peptide standards: (i) a 27-peptide mixture containing three groups of peptides (each group containing nine peptides of the same net charge of +1, +2 or +3), where the hydrophilicity/hydrophobicity of adjacent peptides within the groups varied only subtly (generally by only a single carbon atom); and (ii) peptide pairs with the same composition but different sequences, where the sole difference between the peptides was the position of a single amino acid substitution. HILIC/CEX is essentially CEX chromatography in the presence of high levels of organic modifier (generally ACN). The present study demonstrated the dramatic effect of increasing ACN concentration (optimum levels of 60-80%, depending on the application) on the separation of both mixtures of peptides. The greater the charge on the peptides, the better the separation achievable by HILIC/CEX. In addition, HILIC/CEX separation of both the peptide mixtures used in the present study was shown to be superior to that of the more commonly applied RP-HPLC mode. Our results highlight again the efficacy of HILIC/CEX as a peptide separation mode in its own right as well as an excellent complement to RP-HPLC.</abstract><cop>Weinheim</cop><pub>Wiley-VCH Verlag</pub><pmid>18461566</pmid><doi>10.1002/jssc.200700619</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Amino Acid Sequence Cation-exchange chromatography Chromatography, High Pressure Liquid - methods Chromatography, Ion Exchange - methods Chromatography, Ion Exchange - standards Chromatography, Liquid - methods Chromatography, Liquid - standards Electrochemistry Hydrophilic interaction Hydrophobic and Hydrophilic Interactions Indicators and Reagents Ion-interaction capillary zone electrophoresis Oligopeptides - chemistry Oligopeptides - isolation & purification Oligopeptides - standards Peptides Reference Standards Reversed-phase high-performance liquid chromatography Solvents |
title | Mixed-mode hydrophilic interaction/cation-exchange chromatography: Separation of complex mixtures of peptides of varying charge and hydrophobicity |
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