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Protein profiling of human plasma samples by two-dimensional electrophoresis.

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Bibliographic Details
Title: Protein profiling of human plasma samples by two-dimensional electrophoresis.
Contributors: Sang Yun Cho, Eun-Young Lee, Hye-Young Kim, Min-Jung Kang, Hyoung-Joo Lee, Hoguen Kim, Young-Ki Paik, Kim, Ho Keun
Publication Year: 2008
Subject Terms: Biomarkers, Tumor/blood, Blood Protein Electrophoresis/methods, Blood Proteins/isolation & purification, Carcinoma, Hepatocellular/blood, Chromatography, Affinity, High Pressure Liquid, Electrophoresis, Gel, Two-Dimensional/methods, Humans, Isoelectric Focusing, Liver Neoplasms/blood, Peptide Mapping, Protein Array Analysis/methods, Proteome/isolation & purification, Proteomics/methods, Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization, Staining and Labeling
Description: Human plasma is regarded the most complex and well-known clinical specimen that can be easily obtained; alterations in the levels of plasma proteins or their corresponding enzyme activities may reflect either a healthy or a diseased state. Given that there is no defined genomic information as to the intact protein components in plasma, protein profiling could be the first step toward its molecular characterization. Several problems exist in the analysis of plasma proteins, however. For example, the widest dynamic range of protein concentrations, the presence of high-abundance proteins, and post-translational modifications need to be considered before proteomic studies are undertaken. In particular, efficient depletion or pre-fractionation of high-abundance proteins is crucial for the identification of low-abundance proteins that may contain potential biomarkers. After the removal of high-abundance proteins, protein profiling can be initiated using two-dimensional electrophoresis (2DE), which has been widely used for displaying the differential proteome under specific physiological conditions. Here, we describe a typical 2DE procedure for plasma proteome under either a healthy or a diseased state (e.g., liver cancer) in which pre-fractionation and depletion are integral steps in the search for disease biomarkers. ; open
Document Type: article in journal/newspaper
File Description: 57~75
Language: unknown
Relation: Methods in Molecular Biology (Clifton, N.J.); J02226; https://ir.ymlib.yonsei.ac.kr/handle/22282913/107578; T200801286
Availability: https://ir.ymlib.yonsei.ac.kr/handle/22282913/107578
http://link.springer.com/protocol/10.1007%2F978-1-59745-117-8_4
Rights: CC BY-NC-ND 2.0 KR ; https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ ; not free
Accession Number: edsbas.2213C98F
Database: BASE
Description
Abstract:Human plasma is regarded the most complex and well-known clinical specimen that can be easily obtained; alterations in the levels of plasma proteins or their corresponding enzyme activities may reflect either a healthy or a diseased state. Given that there is no defined genomic information as to the intact protein components in plasma, protein profiling could be the first step toward its molecular characterization. Several problems exist in the analysis of plasma proteins, however. For example, the widest dynamic range of protein concentrations, the presence of high-abundance proteins, and post-translational modifications need to be considered before proteomic studies are undertaken. In particular, efficient depletion or pre-fractionation of high-abundance proteins is crucial for the identification of low-abundance proteins that may contain potential biomarkers. After the removal of high-abundance proteins, protein profiling can be initiated using two-dimensional electrophoresis (2DE), which has been widely used for displaying the differential proteome under specific physiological conditions. Here, we describe a typical 2DE procedure for plasma proteome under either a healthy or a diseased state (e.g., liver cancer) in which pre-fractionation and depletion are integral steps in the search for disease biomarkers. ; open