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A novel general and efficient technique for dissociating antigen in circulating immune complexes
Circulating immune complexes (CICs) are produced during the immune response. It is more clinically important to establish a general and efficient CICs dissociation technique for the detection of antigens for CICs other than the detection of free antigens in the serum. Polyethylene glycol (PEG) two‐p...
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Published in: | Electrophoresis 2018-01, Vol.39 (2), p.406-416 |
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creator | Dai, Yuzhu Hu, Zhengjun Chen, Yu Lou, Bin Cui, Dawei Xu, Aifang Rao, Yueli He, Jiahui Yang, Jiezuan Zeng, Xianming Xu, Xujian Wang, Guozheng Xu, Jian Zhou, Tieli Sun, Changgui Cheng, Jun |
description | Circulating immune complexes (CICs) are produced during the immune response. It is more clinically important to establish a general and efficient CICs dissociation technique for the detection of antigens for CICs other than the detection of free antigens in the serum. Polyethylene glycol (PEG) two‐precipitation separation and glycine‐HCl as a buffer system were employed to develop a general and efficient buffer dissociation technique to separate CICs from serum and dissociate antigens from CICs. The measurement value of new PEG two‐precipitation separation technique was higher than traditional PEG precipitation separation technique. There were slight differences in the dissociation conditions of HCV Core‐IC, HIV P24‐IC, Ins‐IC and TG‐IC as compared to HBsAg‐IC. The detection of antigens in HBsAg‐IC, HCV Core‐IC, HIV P24‐IC, Ins‐IC and TG‐IC with this technique was superior to that with HCl Dissociation, Trypsin Digestion or Immune Complex Transfer technique. PEG two‐precipitation dissociation technique may reduce macromolecular protein and the adhesion of free antigens during the co‐precipitation, which increases the efficiency of separation and precipitation of CICs. This technique also avoids the damage of reagents to antigens, assuring the repeatability, reliability and validity. Thus, this technique is application in samples negative or positive for free antigens. |
doi_str_mv | 10.1002/elps.201700246 |
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It is more clinically important to establish a general and efficient CICs dissociation technique for the detection of antigens for CICs other than the detection of free antigens in the serum. Polyethylene glycol (PEG) two‐precipitation separation and glycine‐HCl as a buffer system were employed to develop a general and efficient buffer dissociation technique to separate CICs from serum and dissociate antigens from CICs. The measurement value of new PEG two‐precipitation separation technique was higher than traditional PEG precipitation separation technique. There were slight differences in the dissociation conditions of HCV Core‐IC, HIV P24‐IC, Ins‐IC and TG‐IC as compared to HBsAg‐IC. The detection of antigens in HBsAg‐IC, HCV Core‐IC, HIV P24‐IC, Ins‐IC and TG‐IC with this technique was superior to that with HCl Dissociation, Trypsin Digestion or Immune Complex Transfer technique. PEG two‐precipitation dissociation technique may reduce macromolecular protein and the adhesion of free antigens during the co‐precipitation, which increases the efficiency of separation and precipitation of CICs. This technique also avoids the damage of reagents to antigens, assuring the repeatability, reliability and validity. Thus, this technique is application in samples negative or positive for free antigens.</description><identifier>ISSN: 0173-0835</identifier><identifier>EISSN: 1522-2683</identifier><identifier>DOI: 10.1002/elps.201700246</identifier><identifier>PMID: 28972666</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Antigen-Antibody Complex - blood ; Antigen-Antibody Complex - chemistry ; Antigen-Antibody Complex - isolation & purification ; Antigens ; Buffers ; Case-Control Studies ; Chemical Precipitation ; Circulating immune complexes ; Coprecipitation ; Enzyme-Linked Immunosorbent Assay ; Glycine ; Glycine - chemistry ; Glycine‐HCl ; Hepatitis B - blood ; Hepatitis B - immunology ; Hepatitis B Antibodies - blood ; Hepatitis B Antibodies - chemistry ; Hepatitis B Antibodies - isolation & purification ; Hepatitis B Surface Antigens - blood ; Hepatitis B Surface Antigens - chemistry ; Hepatitis B Surface Antigens - isolation & purification ; HIV ; Human immunodeficiency virus ; Humans ; Immune system ; Polyethylene glycol ; Polyethylene Glycols - chemistry ; Precipitation separation technique ; Reagents ; Separation ; Trypsin</subject><ispartof>Electrophoresis, 2018-01, Vol.39 (2), p.406-416</ispartof><rights>2017 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><rights>2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4057-1a19d2419816fb6ea50c59cc184dcb1994b8f6285a633c1a4e0bb8d511ba64e33</citedby><cites>FETCH-LOGICAL-c4057-1a19d2419816fb6ea50c59cc184dcb1994b8f6285a633c1a4e0bb8d511ba64e33</cites><orcidid>0000-0002-5149-2776</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28972666$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dai, Yuzhu</creatorcontrib><creatorcontrib>Hu, Zhengjun</creatorcontrib><creatorcontrib>Chen, Yu</creatorcontrib><creatorcontrib>Lou, Bin</creatorcontrib><creatorcontrib>Cui, Dawei</creatorcontrib><creatorcontrib>Xu, Aifang</creatorcontrib><creatorcontrib>Rao, Yueli</creatorcontrib><creatorcontrib>He, Jiahui</creatorcontrib><creatorcontrib>Yang, Jiezuan</creatorcontrib><creatorcontrib>Zeng, Xianming</creatorcontrib><creatorcontrib>Xu, Xujian</creatorcontrib><creatorcontrib>Wang, Guozheng</creatorcontrib><creatorcontrib>Xu, Jian</creatorcontrib><creatorcontrib>Zhou, Tieli</creatorcontrib><creatorcontrib>Sun, Changgui</creatorcontrib><creatorcontrib>Cheng, Jun</creatorcontrib><title>A novel general and efficient technique for dissociating antigen in circulating immune complexes</title><title>Electrophoresis</title><addtitle>Electrophoresis</addtitle><description>Circulating immune complexes (CICs) are produced during the immune response. It is more clinically important to establish a general and efficient CICs dissociation technique for the detection of antigens for CICs other than the detection of free antigens in the serum. Polyethylene glycol (PEG) two‐precipitation separation and glycine‐HCl as a buffer system were employed to develop a general and efficient buffer dissociation technique to separate CICs from serum and dissociate antigens from CICs. The measurement value of new PEG two‐precipitation separation technique was higher than traditional PEG precipitation separation technique. There were slight differences in the dissociation conditions of HCV Core‐IC, HIV P24‐IC, Ins‐IC and TG‐IC as compared to HBsAg‐IC. The detection of antigens in HBsAg‐IC, HCV Core‐IC, HIV P24‐IC, Ins‐IC and TG‐IC with this technique was superior to that with HCl Dissociation, Trypsin Digestion or Immune Complex Transfer technique. PEG two‐precipitation dissociation technique may reduce macromolecular protein and the adhesion of free antigens during the co‐precipitation, which increases the efficiency of separation and precipitation of CICs. This technique also avoids the damage of reagents to antigens, assuring the repeatability, reliability and validity. 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Hu, Zhengjun ; Chen, Yu ; Lou, Bin ; Cui, Dawei ; Xu, Aifang ; Rao, Yueli ; He, Jiahui ; Yang, Jiezuan ; Zeng, Xianming ; Xu, Xujian ; Wang, Guozheng ; Xu, Jian ; Zhou, Tieli ; Sun, Changgui ; Cheng, Jun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4057-1a19d2419816fb6ea50c59cc184dcb1994b8f6285a633c1a4e0bb8d511ba64e33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Antigen-Antibody Complex - blood</topic><topic>Antigen-Antibody Complex - chemistry</topic><topic>Antigen-Antibody Complex - isolation & purification</topic><topic>Antigens</topic><topic>Buffers</topic><topic>Case-Control Studies</topic><topic>Chemical Precipitation</topic><topic>Circulating immune complexes</topic><topic>Coprecipitation</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Glycine</topic><topic>Glycine - chemistry</topic><topic>Glycine‐HCl</topic><topic>Hepatitis B - blood</topic><topic>Hepatitis B - immunology</topic><topic>Hepatitis B Antibodies - blood</topic><topic>Hepatitis B Antibodies - chemistry</topic><topic>Hepatitis B Antibodies - isolation & purification</topic><topic>Hepatitis B Surface Antigens - blood</topic><topic>Hepatitis B Surface Antigens - chemistry</topic><topic>Hepatitis B Surface Antigens - isolation & purification</topic><topic>HIV</topic><topic>Human immunodeficiency virus</topic><topic>Humans</topic><topic>Immune system</topic><topic>Polyethylene glycol</topic><topic>Polyethylene Glycols - chemistry</topic><topic>Precipitation separation technique</topic><topic>Reagents</topic><topic>Separation</topic><topic>Trypsin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dai, Yuzhu</creatorcontrib><creatorcontrib>Hu, Zhengjun</creatorcontrib><creatorcontrib>Chen, Yu</creatorcontrib><creatorcontrib>Lou, Bin</creatorcontrib><creatorcontrib>Cui, Dawei</creatorcontrib><creatorcontrib>Xu, Aifang</creatorcontrib><creatorcontrib>Rao, Yueli</creatorcontrib><creatorcontrib>He, Jiahui</creatorcontrib><creatorcontrib>Yang, Jiezuan</creatorcontrib><creatorcontrib>Zeng, Xianming</creatorcontrib><creatorcontrib>Xu, Xujian</creatorcontrib><creatorcontrib>Wang, Guozheng</creatorcontrib><creatorcontrib>Xu, Jian</creatorcontrib><creatorcontrib>Zhou, Tieli</creatorcontrib><creatorcontrib>Sun, Changgui</creatorcontrib><creatorcontrib>Cheng, Jun</creatorcontrib><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><jtitle>Electrophoresis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dai, Yuzhu</au><au>Hu, Zhengjun</au><au>Chen, Yu</au><au>Lou, Bin</au><au>Cui, Dawei</au><au>Xu, Aifang</au><au>Rao, Yueli</au><au>He, Jiahui</au><au>Yang, Jiezuan</au><au>Zeng, Xianming</au><au>Xu, Xujian</au><au>Wang, Guozheng</au><au>Xu, Jian</au><au>Zhou, Tieli</au><au>Sun, Changgui</au><au>Cheng, Jun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A novel general and efficient technique for dissociating antigen in circulating immune complexes</atitle><jtitle>Electrophoresis</jtitle><addtitle>Electrophoresis</addtitle><date>2018-01</date><risdate>2018</risdate><volume>39</volume><issue>2</issue><spage>406</spage><epage>416</epage><pages>406-416</pages><issn>0173-0835</issn><eissn>1522-2683</eissn><abstract>Circulating immune complexes (CICs) are produced during the immune response. It is more clinically important to establish a general and efficient CICs dissociation technique for the detection of antigens for CICs other than the detection of free antigens in the serum. Polyethylene glycol (PEG) two‐precipitation separation and glycine‐HCl as a buffer system were employed to develop a general and efficient buffer dissociation technique to separate CICs from serum and dissociate antigens from CICs. The measurement value of new PEG two‐precipitation separation technique was higher than traditional PEG precipitation separation technique. There were slight differences in the dissociation conditions of HCV Core‐IC, HIV P24‐IC, Ins‐IC and TG‐IC as compared to HBsAg‐IC. The detection of antigens in HBsAg‐IC, HCV Core‐IC, HIV P24‐IC, Ins‐IC and TG‐IC with this technique was superior to that with HCl Dissociation, Trypsin Digestion or Immune Complex Transfer technique. PEG two‐precipitation dissociation technique may reduce macromolecular protein and the adhesion of free antigens during the co‐precipitation, which increases the efficiency of separation and precipitation of CICs. This technique also avoids the damage of reagents to antigens, assuring the repeatability, reliability and validity. Thus, this technique is application in samples negative or positive for free antigens.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>28972666</pmid><doi>10.1002/elps.201700246</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-5149-2776</orcidid></addata></record> |
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subjects | Antigen-Antibody Complex - blood Antigen-Antibody Complex - chemistry Antigen-Antibody Complex - isolation & purification Antigens Buffers Case-Control Studies Chemical Precipitation Circulating immune complexes Coprecipitation Enzyme-Linked Immunosorbent Assay Glycine Glycine - chemistry Glycine‐HCl Hepatitis B - blood Hepatitis B - immunology Hepatitis B Antibodies - blood Hepatitis B Antibodies - chemistry Hepatitis B Antibodies - isolation & purification Hepatitis B Surface Antigens - blood Hepatitis B Surface Antigens - chemistry Hepatitis B Surface Antigens - isolation & purification HIV Human immunodeficiency virus Humans Immune system Polyethylene glycol Polyethylene Glycols - chemistry Precipitation separation technique Reagents Separation Trypsin |
title | A novel general and efficient technique for dissociating antigen in circulating immune complexes |
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