Ultrahigh-pressure dual online solid phase extraction/capillary reverse-phase liquid chromatography/tandem mass spectrometry (DO-SPE/cRPLC/MS/MS): A versatile separation platform for high-throughput and highly sensitive proteomic analyses

被引:19
作者
Min, Hye-Ki
Hyung, Seok-Won
Shin, Joong-Won
Nam, Hui-Sun
Ahn, Sung-Hyun
Jung, Hee Jung
Lee, Sang-Won
机构
[1] Korea Univ, Dept Chem, Seoul 136701, South Korea
[2] Korea Univ, Ctr Electro & Photo Respons Mol, Seoul 136701, South Korea
[3] Seoul Natl Univ, Imagene Co Ltd, Biotechnol Incubating Ctr, Seoul, South Korea
关键词
ESI; liquid chromatography; MS; proteomics; SPE;
D O I
10.1002/elps.200600501
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Capillary RPLC/ESI-MS (cRPLC/ESI-MS) is one of the most powerful analytical tools for current proteomic research. The development of cRPLC techniques coupled online to a mass spectrometer has focused on increasing the separation efficiency, detection sensitivity, and throughput. Recently, the use of high-pressure (over 10 000 psi) LC systems that utilize long, small inner diameter capillary columns has gained much attention for proteomic analyses. In this study, we developed an ultrahigh-pressure dual online SPE/capillary RPLC (DO-SPE/cRPLC) system. This LC system employs two online SPE columns and two capillary columns (75 mu m inner diameter x 1 m length) in a single separation system, and has a maximum operating pressure of 10 000 psi. This DO-SPE/cRPLC system is capable of providing high-resolution separation in addition to several other advantageous features, such as high reproducibility in terms of the LC retention time, rapid sample injection, online desalting, online sample enrichment of dilute samples, and increased throughput as a result of essentially removing the column equilibration time between successive experiments. We coupled the DO-SPE/cRPLC system online to a tandem mass spectrometer to allow high-throughput proteomic analyses. In this paper, we demonstrate the efficiency of this DO-SPE/cRPLC/MS/MS system by its use in the analyses of proteomic samples exhibiting different levels of complexity.
引用
收藏
页码:1012 / 1021
页数:10
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