A new chromatographic method for fast separation of active proteins

Abstract A new method with only a single chromatographic column to accomplish the separation of intact protein molecules by the combination of ion exchange chromatography and hydrophobic interaction chromatography is firstly presented. By selecting twice a suitable stationary phase, mobile phase, bu...
Ausführliche Beschreibung

Gespeichert in:

Autor*in:	CongYu, Ke [verfasserIn] XinDu, Geng [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2008

Schlagwörter:	proteomics protein pre-fractionation two-dimensional liquid chromatography hydrophobic interaction chromatography ion exchange chromatography

Übergeordnetes Werk:	Enthalten in: Chinese science bulletin - Beijing, China : Chinese Acad. of Sciences, 1997, 53(2008), 7 vom: Apr., Seite 1113-1116
Übergeordnetes Werk:	volume:53 ; year:2008 ; number:7 ; month:04 ; pages:1113-1116

Links:	Volltext

DOI / URN:	10.1007/s11434-008-0179-7

Katalog-ID:	SPR019380836

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520			\|a Abstract A new method with only a single chromatographic column to accomplish the separation of intact protein molecules by the combination of ion exchange chromatography and hydrophobic interaction chromatography is firstly presented. By selecting twice a suitable stationary phase, mobile phase, buffer exchange condition, and sample injection, some proteins usually required to separate with two-dimensional chromatography can now be accomplished only using the single column in one hour. In addition, the separated proteins can maintain their original three- or four-dimensional molecular structure. It would be expected that this method can also provide a new thought for sample pre-fractionation in proteomic investigation, especially, for the limitation of sample source.
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650		4	\|a hydrophobic interaction chromatography \|7 (dpeaa)DE-He213
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spelling	10.1007/s11434-008-0179-7 doi (DE-627)SPR019380836 (SPR)s11434-008-0179-7-e DE-627 ger DE-627 rakwb eng 500 ASE 30.00 bkl CongYu, Ke verfasserin aut A new chromatographic method for fast separation of active proteins 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A new method with only a single chromatographic column to accomplish the separation of intact protein molecules by the combination of ion exchange chromatography and hydrophobic interaction chromatography is firstly presented. By selecting twice a suitable stationary phase, mobile phase, buffer exchange condition, and sample injection, some proteins usually required to separate with two-dimensional chromatography can now be accomplished only using the single column in one hour. In addition, the separated proteins can maintain their original three- or four-dimensional molecular structure. It would be expected that this method can also provide a new thought for sample pre-fractionation in proteomic investigation, especially, for the limitation of sample source. proteomics (dpeaa)DE-He213 protein pre-fractionation (dpeaa)DE-He213 two-dimensional liquid chromatography (dpeaa)DE-He213 hydrophobic interaction chromatography (dpeaa)DE-He213 ion exchange chromatography (dpeaa)DE-He213 XinDu, Geng verfasserin aut Enthalten in Chinese science bulletin Beijing, China : Chinese Acad. of Sciences, 1997 53(2008), 7 vom: Apr., Seite 1113-1116 (DE-627)341897809 (DE-600)2069521-4 1861-9541 nnns volume:53 year:2008 number:7 month:04 pages:1113-1116 https://dx.doi.org/10.1007/s11434-008-0179-7 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_20 GBV_ILN_40 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_110 GBV_ILN_120 GBV_ILN_161 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2055 GBV_ILN_2059 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4313 GBV_ILN_4328 GBV_ILN_4333 30.00 ASE AR 53 2008 7 04 1113-1116
allfields_unstemmed	10.1007/s11434-008-0179-7 doi (DE-627)SPR019380836 (SPR)s11434-008-0179-7-e DE-627 ger DE-627 rakwb eng 500 ASE 30.00 bkl CongYu, Ke verfasserin aut A new chromatographic method for fast separation of active proteins 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A new method with only a single chromatographic column to accomplish the separation of intact protein molecules by the combination of ion exchange chromatography and hydrophobic interaction chromatography is firstly presented. By selecting twice a suitable stationary phase, mobile phase, buffer exchange condition, and sample injection, some proteins usually required to separate with two-dimensional chromatography can now be accomplished only using the single column in one hour. In addition, the separated proteins can maintain their original three- or four-dimensional molecular structure. It would be expected that this method can also provide a new thought for sample pre-fractionation in proteomic investigation, especially, for the limitation of sample source. proteomics (dpeaa)DE-He213 protein pre-fractionation (dpeaa)DE-He213 two-dimensional liquid chromatography (dpeaa)DE-He213 hydrophobic interaction chromatography (dpeaa)DE-He213 ion exchange chromatography (dpeaa)DE-He213 XinDu, Geng verfasserin aut Enthalten in Chinese science bulletin Beijing, China : Chinese Acad. of Sciences, 1997 53(2008), 7 vom: Apr., Seite 1113-1116 (DE-627)341897809 (DE-600)2069521-4 1861-9541 nnns volume:53 year:2008 number:7 month:04 pages:1113-1116 https://dx.doi.org/10.1007/s11434-008-0179-7 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_20 GBV_ILN_40 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_110 GBV_ILN_120 GBV_ILN_161 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2055 GBV_ILN_2059 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4313 GBV_ILN_4328 GBV_ILN_4333 30.00 ASE AR 53 2008 7 04 1113-1116
allfieldsGer	10.1007/s11434-008-0179-7 doi (DE-627)SPR019380836 (SPR)s11434-008-0179-7-e DE-627 ger DE-627 rakwb eng 500 ASE 30.00 bkl CongYu, Ke verfasserin aut A new chromatographic method for fast separation of active proteins 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A new method with only a single chromatographic column to accomplish the separation of intact protein molecules by the combination of ion exchange chromatography and hydrophobic interaction chromatography is firstly presented. By selecting twice a suitable stationary phase, mobile phase, buffer exchange condition, and sample injection, some proteins usually required to separate with two-dimensional chromatography can now be accomplished only using the single column in one hour. In addition, the separated proteins can maintain their original three- or four-dimensional molecular structure. It would be expected that this method can also provide a new thought for sample pre-fractionation in proteomic investigation, especially, for the limitation of sample source. proteomics (dpeaa)DE-He213 protein pre-fractionation (dpeaa)DE-He213 two-dimensional liquid chromatography (dpeaa)DE-He213 hydrophobic interaction chromatography (dpeaa)DE-He213 ion exchange chromatography (dpeaa)DE-He213 XinDu, Geng verfasserin aut Enthalten in Chinese science bulletin Beijing, China : Chinese Acad. of Sciences, 1997 53(2008), 7 vom: Apr., Seite 1113-1116 (DE-627)341897809 (DE-600)2069521-4 1861-9541 nnns volume:53 year:2008 number:7 month:04 pages:1113-1116 https://dx.doi.org/10.1007/s11434-008-0179-7 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_20 GBV_ILN_40 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_110 GBV_ILN_120 GBV_ILN_161 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2055 GBV_ILN_2059 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4313 GBV_ILN_4328 GBV_ILN_4333 30.00 ASE AR 53 2008 7 04 1113-1116
allfieldsSound	10.1007/s11434-008-0179-7 doi (DE-627)SPR019380836 (SPR)s11434-008-0179-7-e DE-627 ger DE-627 rakwb eng 500 ASE 30.00 bkl CongYu, Ke verfasserin aut A new chromatographic method for fast separation of active proteins 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A new method with only a single chromatographic column to accomplish the separation of intact protein molecules by the combination of ion exchange chromatography and hydrophobic interaction chromatography is firstly presented. By selecting twice a suitable stationary phase, mobile phase, buffer exchange condition, and sample injection, some proteins usually required to separate with two-dimensional chromatography can now be accomplished only using the single column in one hour. In addition, the separated proteins can maintain their original three- or four-dimensional molecular structure. It would be expected that this method can also provide a new thought for sample pre-fractionation in proteomic investigation, especially, for the limitation of sample source. proteomics (dpeaa)DE-He213 protein pre-fractionation (dpeaa)DE-He213 two-dimensional liquid chromatography (dpeaa)DE-He213 hydrophobic interaction chromatography (dpeaa)DE-He213 ion exchange chromatography (dpeaa)DE-He213 XinDu, Geng verfasserin aut Enthalten in Chinese science bulletin Beijing, China : Chinese Acad. of Sciences, 1997 53(2008), 7 vom: Apr., Seite 1113-1116 (DE-627)341897809 (DE-600)2069521-4 1861-9541 nnns volume:53 year:2008 number:7 month:04 pages:1113-1116 https://dx.doi.org/10.1007/s11434-008-0179-7 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_20 GBV_ILN_40 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_110 GBV_ILN_120 GBV_ILN_161 GBV_ILN_266 GBV_ILN_285 GBV_ILN_293 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2055 GBV_ILN_2059 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4313 GBV_ILN_4328 GBV_ILN_4333 30.00 ASE AR 53 2008 7 04 1113-1116
language	English
source	Enthalten in Chinese science bulletin 53(2008), 7 vom: Apr., Seite 1113-1116 volume:53 year:2008 number:7 month:04 pages:1113-1116
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format_phy_str_mv	Article
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topic_facet	proteomics protein pre-fractionation two-dimensional liquid chromatography hydrophobic interaction chromatography ion exchange chromatography
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container_title	Chinese science bulletin
authorswithroles_txt_mv	CongYu, Ke @@aut@@ XinDu, Geng @@aut@@
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author	CongYu, Ke
spellingShingle	CongYu, Ke ddc 500 bkl 30.00 misc proteomics misc protein pre-fractionation misc two-dimensional liquid chromatography misc hydrophobic interaction chromatography misc ion exchange chromatography A new chromatographic method for fast separation of active proteins
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topic_title	500 ASE 30.00 bkl A new chromatographic method for fast separation of active proteins proteomics (dpeaa)DE-He213 protein pre-fractionation (dpeaa)DE-He213 two-dimensional liquid chromatography (dpeaa)DE-He213 hydrophobic interaction chromatography (dpeaa)DE-He213 ion exchange chromatography (dpeaa)DE-He213
topic	ddc 500 bkl 30.00 misc proteomics misc protein pre-fractionation misc two-dimensional liquid chromatography misc hydrophobic interaction chromatography misc ion exchange chromatography
topic_unstemmed	ddc 500 bkl 30.00 misc proteomics misc protein pre-fractionation misc two-dimensional liquid chromatography misc hydrophobic interaction chromatography misc ion exchange chromatography
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title	A new chromatographic method for fast separation of active proteins
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title_full	A new chromatographic method for fast separation of active proteins
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title_sort	new chromatographic method for fast separation of active proteins
title_auth	A new chromatographic method for fast separation of active proteins
abstract	Abstract A new method with only a single chromatographic column to accomplish the separation of intact protein molecules by the combination of ion exchange chromatography and hydrophobic interaction chromatography is firstly presented. By selecting twice a suitable stationary phase, mobile phase, buffer exchange condition, and sample injection, some proteins usually required to separate with two-dimensional chromatography can now be accomplished only using the single column in one hour. In addition, the separated proteins can maintain their original three- or four-dimensional molecular structure. It would be expected that this method can also provide a new thought for sample pre-fractionation in proteomic investigation, especially, for the limitation of sample source.
abstractGer	Abstract A new method with only a single chromatographic column to accomplish the separation of intact protein molecules by the combination of ion exchange chromatography and hydrophobic interaction chromatography is firstly presented. By selecting twice a suitable stationary phase, mobile phase, buffer exchange condition, and sample injection, some proteins usually required to separate with two-dimensional chromatography can now be accomplished only using the single column in one hour. In addition, the separated proteins can maintain their original three- or four-dimensional molecular structure. It would be expected that this method can also provide a new thought for sample pre-fractionation in proteomic investigation, especially, for the limitation of sample source.
abstract_unstemmed	Abstract A new method with only a single chromatographic column to accomplish the separation of intact protein molecules by the combination of ion exchange chromatography and hydrophobic interaction chromatography is firstly presented. By selecting twice a suitable stationary phase, mobile phase, buffer exchange condition, and sample injection, some proteins usually required to separate with two-dimensional chromatography can now be accomplished only using the single column in one hour. In addition, the separated proteins can maintain their original three- or four-dimensional molecular structure. It would be expected that this method can also provide a new thought for sample pre-fractionation in proteomic investigation, especially, for the limitation of sample source.
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title_short	A new chromatographic method for fast separation of active proteins
url	https://dx.doi.org/10.1007/s11434-008-0179-7
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up_date	2024-07-04T01:20:19.365Z
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A new chromatographic method for fast separation of active proteins

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