Lectin precipitation using phytohemagglutinin-L(4) coupled to avidin-agarose for serological biomarker discovery in colorectal cancer

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dc.contributor.authorYong Sam Kim-
dc.contributor.authorO L Son-
dc.contributor.authorJ Y Lee-
dc.contributor.authorS H Kim-
dc.contributor.authorS Oh-
dc.contributor.authorY S Lee-
dc.contributor.authorC H Kim-
dc.contributor.authorJ S Yoo-
dc.contributor.authorJ H Lee-
dc.contributor.authorE Miyoshi-
dc.contributor.authorN Taniguchi-
dc.contributor.authorS M Hanash-
dc.contributor.authorHyang Sook Yoo-
dc.contributor.authorJeong Heon Ko-
dc.date.accessioned2017-04-19T09:11:23Z-
dc.date.available2017-04-19T09:11:23Z-
dc.date.issued2008-
dc.identifier.issn1615-9853-
dc.identifier.uri10.1002/pmic.200800034ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/8539-
dc.description.abstractN-acetylglucosaminyltransferase V (GnT-V) has been reported to be upregulated in malignant cancer cells, and its targets have been sought after with regard to biomarker identification. The low capacity and high false positive rates of 2-DE gel-based lectin blots using phytohemagglutinin-L 4 (L-PHA) prompted us to develop a novel protocol for identifying GnT-V targets, in which serum proteins were subjected to immunodepletion, alkylation, and lectin precipitation using L-PHA coupled to avidin-agarose bead complexes, and tryptic digestion. Proteins captured by L-PHA conjugates were analyzed by a nano-LC-FT-ICR/LTQ MS. Here, we report 26 candidate biomarkers for colorectal cancer (CRC) that show 100% specificity and sensitivities of greater than 50%. Not only can these candidate proteins be used as analytes for validation, but the novel protocol described herein can be applied to biomarker discovery in nonCRCs.-
dc.publisherWiley-
dc.titleLectin precipitation using phytohemagglutinin-L(4) coupled to avidin-agarose for serological biomarker discovery in colorectal cancer-
dc.title.alternativeLectin precipitation using phytohemagglutinin-L(4) coupled to avidin-agarose for serological biomarker discovery in colorectal cancer-
dc.typeArticle-
dc.citation.titleProteomics-
dc.citation.number16-
dc.citation.endPage3235-
dc.citation.startPage3229-
dc.citation.volume8-
dc.contributor.affiliatedAuthorYong Sam Kim-
dc.contributor.affiliatedAuthorHyang Sook Yoo-
dc.contributor.affiliatedAuthorJeong Heon Ko-
dc.contributor.alternativeName김용삼-
dc.contributor.alternativeName손옥례-
dc.contributor.alternativeName이주연-
dc.contributor.alternativeName김선희-
dc.contributor.alternativeName오세정-
dc.contributor.alternativeName이윤석-
dc.contributor.alternativeName김철호-
dc.contributor.alternativeName유종신-
dc.contributor.alternativeName이정화-
dc.contributor.alternativeNameMiyoshi-
dc.contributor.alternativeNameTaniguchi-
dc.contributor.alternativeNameHanash-
dc.contributor.alternativeName유향숙-
dc.contributor.alternativeName고정헌-
dc.identifier.bibliographicCitationProteomics, vol. 8, no. 16, pp. 3229-3235-
dc.identifier.doi10.1002/pmic.200800034-
dc.subject.keywordBiomarker-
dc.subject.keywordColorectal cancer-
dc.subject.keywordGnT-V-
dc.subject.keywordL-PHA-
dc.subject.localBiomarker-
dc.subject.localBiomarkers-
dc.subject.localbiomarker-
dc.subject.localbio-marker-
dc.subject.localColorectal cancer-
dc.subject.localcolorectal cancer-
dc.subject.localColorectal Cancer-
dc.subject.localGnT-V-
dc.subject.localL-PHA-
dc.description.journalClassY-
Appears in Collections:
Synthetic Biology and Bioengineering Research Institute > Genome Editing Research Center > 1. Journal Articles
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