Capillary electrophoresis-based separation techniques for the analysis of proteins Export

@article{citeulike:940327, abstract = {CE offers the advantages of high speed, great efficiency, as well as the requirement of minimum amounts of sample and buffer for the analysis of proteins. In this review, we summarize the CE-based techniques coupled with absorption, LIF, and MS detection systems for the analysis of proteins mostly within the past 5 years. The basic principle of each technique and its advantages and disadvantages for protein analysis are discussed in brief. Advanced CE techniques, including on-column concentration techniques and high-efficiency multidimensional separation techniques, for high-throughput protein profiling of complex biological samples and/or of single cells are emphasized. Although the developed techniques provide improved peak capacity, they have not become practical tools for proteomics, mainly because of poor reproducibility, low-sample lading capacity, and low throughput due to ineffective interfaces between two separation dimensions and that between separation and MS systems. In order to identify the complexities and dynamics of the proteomes expressed by cells, tissues, or organisms, techniques providing improved analytical sensitivity, throughput, and dynamic ranges are still demanded.}, address = {Department of Chemistry, National Taiwan University, Taipei, Taiwan; Department of Natural Science Education, National TaiTung University, TaiTung, Taiwan}, author = {Huang, Yu-Fen and Huang, Chih-Chin and Hu, Cho-Chun and Chang, Huan-Tsung}, citeulike-article-id = {940327}, citeulike-linkout-0 = {http://dx.doi.org/10.1002/elps.200600100}, citeulike-linkout-1 = {http://www3.interscience.wiley.com/cgi-bin/abstract/112764282/ABSTRACT}, doi = {10.1002/elps.200600100}, journal = {ELECTROPHORESIS}, keywords = {ce}, number = {18}, pages = {3503--3522}, posted-at = {2006-11-11 14:25:31}, priority = {2}, title = {Capillary electrophoresis-based separation techniques for the analysis of proteins}, url = {http://dx.doi.org/10.1002/elps.200600100}, volume = {27}, year = {2006} }

TY - JOUR ID - citeulike:940327 L3 - citeulike-article-id:940327 N2 - CE offers the advantages of high speed, great efficiency, as well as the requirement of minimum amounts of sample and buffer for the analysis of proteins. In this review, we summarize the CE-based techniques coupled with absorption, LIF, and MS detection systems for the analysis of proteins mostly within the past 5 years. The basic principle of each technique and its advantages and disadvantages for protein analysis are discussed in brief. Advanced CE techniques, including on-column concentration techniques and high-efficiency multidimensional separation techniques, for high-throughput protein profiling of complex biological samples and/or of single cells are emphasized. Although the developed techniques provide improved peak capacity, they have not become practical tools for proteomics, mainly because of poor reproducibility, low-sample lading capacity, and low throughput due to ineffective interfaces between two separation dimensions and that between separation and MS systems. In order to identify the complexities and dynamics of the proteomes expressed by cells, tissues, or organisms, techniques providing improved analytical sensitivity, throughput, and dynamic ranges are still demanded. IS - 18 JF - ELECTROPHORESIS AD - Department of Chemistry, National Taiwan University, Taipei, Taiwan; Department of Natural Science Education, National TaiTung University, TaiTung, Taiwan EP - 3522 TI - Capillary electrophoresis-based separation techniques for the analysis of proteins VL - 27 SP - 3503 KW - ce AU - Huang, Yu-Fen AU - Huang, Chih-Chin AU - Hu, Cho-Chun AU - Chang, Huan-Tsung PY - 2006/// UR - http://dx.doi.org/10.1002/elps.200600100 ER -