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Development of a parallel microbore hollow fiber enzyme reactor platform for online 18O-labeling: Application to lectin-specific lung cancer N-glycoproteome.
Lee, Sun Young; Lee, Seonjeong; Park, Sung Bum; Kim, Ki Young; Hong, Jongki; Kang, Dukjin.
Afiliação
  • Lee SY; College of Pharmacy, Kyung Hee University, Seoul 02447, Republic of Korea.
  • Lee S; College of Pharmacy, Kyung Hee University, Seoul 02447, Republic of Korea.
  • Park SB; Therapeutics & Biotechnology Division, Korea Research Institute of Chemical Technology, P.O. Box 107, Yuseong-gu, Daejeon 34134, Republic of Korea.
  • Kim KY; Therapeutics & Biotechnology Division, Korea Research Institute of Chemical Technology, P.O. Box 107, Yuseong-gu, Daejeon 34134, Republic of Korea.
  • Hong J; College of Pharmacy, Kyung Hee University, Seoul 02447, Republic of Korea. Electronic address: jhong@khu.ac.kr.
  • Kang D; Center for Bioanalysis, Division of Chemical and Medical Metrology, Korea Research Institute of Standards and Science, Daejeon, 34113, Republic of Korea. Electronic address: djkang@kriss.re.kr.
J Chromatogr B Analyt Technol Biomed Life Sci ; 1100-1101: 58-64, 2018 Nov 15.
Article em En | MEDLINE | ID: mdl-30292950
ABSTRACT
We introduce a simple online 18O-labeling protocol for protein samples that uses a parallelizing microbore hollow fiber enzyme reactor (mHFER) as an alternative tool for online proteolytic digestion. Online 18O-labeling is performed by separately attaching two mHFERs in parallel to a 10-port switching valve with a high-pressure syringe pump and two syringes containing 16O- or 18O-water. 16O-/18O-labeled peptides are formed in this manner and simultaneously analyzed online using nanoflow liquid chromatography-tandem mass spectrometry (nLC-MS/MS) without any residual trypsin activity. The usefulness of a parallel mHFER platform (P-mHFER) in 18O-labeling was tested using both cytochrome C and alpha-1-acid-glycoprotein to verify the incorporation level of two 18O atoms into tryptic peptides and to provide a quantitative assessment with varied mixing ratios. Additionally, our 18O-labeling approach was used to study the serum N-glycoproteome from lung cancer patients and controls to evaluate the applicability of lectin-based quantitative N-glycoproteomics. We successfully quantified 76 peptides (from 62 N-glycoproteins). Nineteen of these peptides from lung cancer serum were up-/down-regulated at least 2.5-fold compared to controls. As a result, the P-mHFER-based online 18O-labeling platform presented here can be a simple and reproducible way to allow quantitative proteomic analysis of diverse proteome samples.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Isótopos de Oxigênio / Glicoproteínas / Reatores Biológicos / Proteoma / Neoplasias Pulmonares Limite: Humans Idioma: En Revista: J Chromatogr B Analyt Technol Biomed Life Sci Assunto da revista: ENGENHARIA BIOMEDICA Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Isótopos de Oxigênio / Glicoproteínas / Reatores Biológicos / Proteoma / Neoplasias Pulmonares Limite: Humans Idioma: En Revista: J Chromatogr B Analyt Technol Biomed Life Sci Assunto da revista: ENGENHARIA BIOMEDICA Ano de publicação: 2018 Tipo de documento: Article
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