Optimizing Human Bile Preparation for Two-Dimensional Gel Electrophoresis
Aims. Bile is an important body fluid which assists in the digestion of fat and excretion of endogenous and exogenous compounds. In the present study, an improved sample preparation for human bile was established. Methods and Material. The method involved acetone precipitation followed by protein ex...
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description | Aims. Bile is an important body fluid which assists in the digestion of fat and excretion of endogenous and exogenous compounds. In the present study, an improved sample preparation for human bile was established. Methods and Material. The method involved acetone precipitation followed by protein extraction using commercially available 2D Clean-Up kit. The effectiveness was evaluated by 2-dimensional electrophoresis (2DE) profiling quality, including number of protein spots and spot distribution. Results. The total protein of bile fluid in benign biliary disorders was 0.797 ± 0.465 μg/μL. The sample preparation method using acetone precipitation first followed by 2D Clean-Up kit protein extraction resulted in better quality of 2DE gel images in terms of resolution as compared with other sample preparation methods. Using this protocol, we obtained approximately 558 protein spots on the gel images and with better protein spots presentation of haptoglobin, serum albumin, serotransferrin, and transthyretin. Conclusions. Protein samples of bile prepared using acetone precipitation followed by 2D Clean-Up kit exhibited high protein resolution and significant protein profile. This optimized protein preparation protocol can effectively concentrate bile proteins, remove abundant proteins and debris, and yield clear presentation of nonabundant proteins and its isoforms on 2-dimensional electrophoresis gel images. |
doi_str_mv | 10.1155/2016/5185317 |
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Bile is an important body fluid which assists in the digestion of fat and excretion of endogenous and exogenous compounds. In the present study, an improved sample preparation for human bile was established. Methods and Material. The method involved acetone precipitation followed by protein extraction using commercially available 2D Clean-Up kit. The effectiveness was evaluated by 2-dimensional electrophoresis (2DE) profiling quality, including number of protein spots and spot distribution. Results. The total protein of bile fluid in benign biliary disorders was 0.797 ± 0.465 μg/μL. The sample preparation method using acetone precipitation first followed by 2D Clean-Up kit protein extraction resulted in better quality of 2DE gel images in terms of resolution as compared with other sample preparation methods. Using this protocol, we obtained approximately 558 protein spots on the gel images and with better protein spots presentation of haptoglobin, serum albumin, serotransferrin, and transthyretin. Conclusions. Protein samples of bile prepared using acetone precipitation followed by 2D Clean-Up kit exhibited high protein resolution and significant protein profile. This optimized protein preparation protocol can effectively concentrate bile proteins, remove abundant proteins and debris, and yield clear presentation of nonabundant proteins and its isoforms on 2-dimensional electrophoresis gel images.</description><identifier>ISSN: 2314-6133</identifier><identifier>EISSN: 2314-6141</identifier><identifier>DOI: 10.1155/2016/5185317</identifier><identifier>PMID: 26966686</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Acetone ; Acetone - chemistry ; Albumin ; Bile ; Bile - metabolism ; Biomarkers ; Body fluids ; Electrophoresis ; Electrophoresis, Gel, Two-Dimensional - methods ; Fluids ; Gallbladder diseases ; Gastroenterology ; Grants ; Haptoglobin ; Hospitals ; Humans ; Liver diseases ; Medicine ; Methods ; Precipitation (Meteorology) ; Protein Biosynthesis - genetics ; Proteins ; Proteome - genetics ; Proteome - isolation & purification ; Proteome - metabolism ; Proteomics ; Proteomics - methods ; Studies ; University colleges</subject><ispartof>BioMed research international, 2016-01, Vol.2016 (2016), p.1-6</ispartof><rights>Copyright © 2016 Hao-Tsai Cheng et al.</rights><rights>COPYRIGHT 2016 John Wiley & Sons, Inc.</rights><rights>Copyright © 2016 Hao-Tsai Cheng et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright © 2016 Hao-Tsai Cheng et al. 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c532t-8c3b8ba38b5752abf2b05820af42a71493c3be134e8eff527010559ec3a896fa3</citedby><cites>FETCH-LOGICAL-c532t-8c3b8ba38b5752abf2b05820af42a71493c3be134e8eff527010559ec3a896fa3</cites><orcidid>0000-0002-1723-7261</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4757711/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4757711/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26966686$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Stockinger, Hannes</contributor><creatorcontrib>Liu, Nai-Jen</creatorcontrib><creatorcontrib>Pai, Betty Chien-Jung</creatorcontrib><creatorcontrib>Sung, Chang-Mu</creatorcontrib><creatorcontrib>Hsieh, Sen-Yung</creatorcontrib><creatorcontrib>Cheng, Hao-Tsai</creatorcontrib><creatorcontrib>Chen, Carl PC</creatorcontrib><title>Optimizing Human Bile Preparation for Two-Dimensional Gel Electrophoresis</title><title>BioMed research international</title><addtitle>Biomed Res Int</addtitle><description>Aims. Bile is an important body fluid which assists in the digestion of fat and excretion of endogenous and exogenous compounds. In the present study, an improved sample preparation for human bile was established. Methods and Material. The method involved acetone precipitation followed by protein extraction using commercially available 2D Clean-Up kit. The effectiveness was evaluated by 2-dimensional electrophoresis (2DE) profiling quality, including number of protein spots and spot distribution. Results. The total protein of bile fluid in benign biliary disorders was 0.797 ± 0.465 μg/μL. The sample preparation method using acetone precipitation first followed by 2D Clean-Up kit protein extraction resulted in better quality of 2DE gel images in terms of resolution as compared with other sample preparation methods. Using this protocol, we obtained approximately 558 protein spots on the gel images and with better protein spots presentation of haptoglobin, serum albumin, serotransferrin, and transthyretin. Conclusions. Protein samples of bile prepared using acetone precipitation followed by 2D Clean-Up kit exhibited high protein resolution and significant protein profile. This optimized protein preparation protocol can effectively concentrate bile proteins, remove abundant proteins and debris, and yield clear presentation of nonabundant proteins and its isoforms on 2-dimensional electrophoresis gel images.</description><subject>Acetone</subject><subject>Acetone - chemistry</subject><subject>Albumin</subject><subject>Bile</subject><subject>Bile - metabolism</subject><subject>Biomarkers</subject><subject>Body fluids</subject><subject>Electrophoresis</subject><subject>Electrophoresis, Gel, Two-Dimensional - methods</subject><subject>Fluids</subject><subject>Gallbladder diseases</subject><subject>Gastroenterology</subject><subject>Grants</subject><subject>Haptoglobin</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Liver diseases</subject><subject>Medicine</subject><subject>Methods</subject><subject>Precipitation (Meteorology)</subject><subject>Protein Biosynthesis - genetics</subject><subject>Proteins</subject><subject>Proteome - genetics</subject><subject>Proteome - isolation & purification</subject><subject>Proteome - metabolism</subject><subject>Proteomics</subject><subject>Proteomics - methods</subject><subject>Studies</subject><subject>University colleges</subject><issn>2314-6133</issn><issn>2314-6141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>RHX</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqN0c1PFDEYBvDGSIQgN89mEi8mOtK3nX7MxQQRgYQEDnhuOsPb3ZKZ6djOSOSvp-uuK3CilzbtL0_aPoS8A_oFQIhDRkEeCtCCg3pF9hiHqpRQwevtmvNdcpDSLc1Dg6S1fEN2mayllFrukfPLcfK9v_fDojibezsU33yHxVXE0UY7-TAULsTi-i6U332PQ8o7titOsStOOmynGMZliJh8ekt2nO0SHmzmffLzx8n18Vl5cXl6fnx0UbaCs6nULW90Y7luhBLMNo41VGhGrauYVVDVPAMEXqFG5wRTFKgQNbbc6lo6y_fJ13XuODc93rQ4TNF2Zoy-t_GPCdabpyeDX5pF-G0qJZQCyAEfNwEx_JoxTab3qcWuswOGORlQimkOVFYvoFILVXG-oh-e0dswx_xXf5WgSnKt_quF7dD4wYV8xXYVao4EowpylzKrz2vVxpBSRLd9HVCz6t2sejeb3jN___hHtvhfyxl8WoOlH27snX9hHGaDzj7StaZM8AcyH7zE</recordid><startdate>20160101</startdate><enddate>20160101</enddate><creator>Liu, Nai-Jen</creator><creator>Pai, Betty Chien-Jung</creator><creator>Sung, Chang-Mu</creator><creator>Hsieh, Sen-Yung</creator><creator>Cheng, Hao-Tsai</creator><creator>Chen, Carl PC</creator><general>Hindawi Publishing Corporation</general><general>John Wiley & Sons, Inc</general><general>Hindawi Limited</general><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</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>3V.</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>CWDGH</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-1723-7261</orcidid></search><sort><creationdate>20160101</creationdate><title>Optimizing Human Bile Preparation for Two-Dimensional Gel Electrophoresis</title><author>Liu, Nai-Jen ; Pai, Betty Chien-Jung ; Sung, Chang-Mu ; Hsieh, Sen-Yung ; Cheng, Hao-Tsai ; Chen, Carl PC</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c532t-8c3b8ba38b5752abf2b05820af42a71493c3be134e8eff527010559ec3a896fa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Acetone</topic><topic>Acetone - chemistry</topic><topic>Albumin</topic><topic>Bile</topic><topic>Bile - metabolism</topic><topic>Biomarkers</topic><topic>Body fluids</topic><topic>Electrophoresis</topic><topic>Electrophoresis, Gel, Two-Dimensional - methods</topic><topic>Fluids</topic><topic>Gallbladder diseases</topic><topic>Gastroenterology</topic><topic>Grants</topic><topic>Haptoglobin</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Liver diseases</topic><topic>Medicine</topic><topic>Methods</topic><topic>Precipitation (Meteorology)</topic><topic>Protein Biosynthesis - genetics</topic><topic>Proteins</topic><topic>Proteome - genetics</topic><topic>Proteome - isolation & purification</topic><topic>Proteome - metabolism</topic><topic>Proteomics</topic><topic>Proteomics - methods</topic><topic>Studies</topic><topic>University colleges</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Nai-Jen</creatorcontrib><creatorcontrib>Pai, Betty Chien-Jung</creatorcontrib><creatorcontrib>Sung, Chang-Mu</creatorcontrib><creatorcontrib>Hsieh, Sen-Yung</creatorcontrib><creatorcontrib>Cheng, Hao-Tsai</creatorcontrib><creatorcontrib>Chen, Carl PC</creatorcontrib><collection>الدوريات العلمية والإحصائية - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BioMed research international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Nai-Jen</au><au>Pai, Betty Chien-Jung</au><au>Sung, Chang-Mu</au><au>Hsieh, Sen-Yung</au><au>Cheng, Hao-Tsai</au><au>Chen, Carl PC</au><au>Stockinger, Hannes</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Optimizing Human Bile Preparation for Two-Dimensional Gel Electrophoresis</atitle><jtitle>BioMed research international</jtitle><addtitle>Biomed Res Int</addtitle><date>2016-01-01</date><risdate>2016</risdate><volume>2016</volume><issue>2016</issue><spage>1</spage><epage>6</epage><pages>1-6</pages><issn>2314-6133</issn><eissn>2314-6141</eissn><abstract>Aims. Bile is an important body fluid which assists in the digestion of fat and excretion of endogenous and exogenous compounds. In the present study, an improved sample preparation for human bile was established. Methods and Material. The method involved acetone precipitation followed by protein extraction using commercially available 2D Clean-Up kit. The effectiveness was evaluated by 2-dimensional electrophoresis (2DE) profiling quality, including number of protein spots and spot distribution. Results. The total protein of bile fluid in benign biliary disorders was 0.797 ± 0.465 μg/μL. The sample preparation method using acetone precipitation first followed by 2D Clean-Up kit protein extraction resulted in better quality of 2DE gel images in terms of resolution as compared with other sample preparation methods. Using this protocol, we obtained approximately 558 protein spots on the gel images and with better protein spots presentation of haptoglobin, serum albumin, serotransferrin, and transthyretin. Conclusions. Protein samples of bile prepared using acetone precipitation followed by 2D Clean-Up kit exhibited high protein resolution and significant protein profile. This optimized protein preparation protocol can effectively concentrate bile proteins, remove abundant proteins and debris, and yield clear presentation of nonabundant proteins and its isoforms on 2-dimensional electrophoresis gel images.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>26966686</pmid><doi>10.1155/2016/5185317</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-1723-7261</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acetone Acetone - chemistry Albumin Bile Bile - metabolism Biomarkers Body fluids Electrophoresis Electrophoresis, Gel, Two-Dimensional - methods Fluids Gallbladder diseases Gastroenterology Grants Haptoglobin Hospitals Humans Liver diseases Medicine Methods Precipitation (Meteorology) Protein Biosynthesis - genetics Proteins Proteome - genetics Proteome - isolation & purification Proteome - metabolism Proteomics Proteomics - methods Studies University colleges |
title | Optimizing Human Bile Preparation for Two-Dimensional Gel Electrophoresis |
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