Development of an Online 2D Ultrahigh-Pressure Nano-LC System for High-pH and Low-pH Reversed Phase Separation in Top-Down Proteomics

被引:21
|
作者
Wang, Zhe [1 ]
Yu, Dahang [1 ]
Cupp-Sutton, Kellye A. [1 ]
Liu, Xiaowen [2 ]
Smith, Kenneth [3 ]
Wu, Si [1 ]
机构
[1] Univ Oklahoma, Dept Chem & Biochem, Norman, OK 73019 USA
[2] Indiana Univ Purdue Univ, Sch Informat & Comp, Indianapolis, IN 46202 USA
[3] Oklahoma Med Res Fdn, Arthrit & Clin Immunol Res Program, Oklahoma City, OK 73104 USA
关键词
EFFECTIVE PROTEIN SEPARATION; MASS-SPECTROMETRY; LIQUID-CHROMATOGRAPHY; HYDROPHILIC INTERACTION; BOTTOM-UP;
D O I
10.1021/acs.analchem.0c03395
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The development of novel high-resolution separation techniques is crucial for advancing the complex sample analysis necessary for high-throughput top-down proteomics. Recently, our group developed an offline 2D high-pH RPLC/low-pH RPLC separation method and demonstrated good orthogonality between these two RPLC formats. Specifically, ultrahigh-pressure long capillary column RPLC separation has been applied as the second dimensional low-pH RPLC separation for the improvement of separation resolution. To further improve the throughput and sensitivity of the offline approach, we developed an online 2D ultrahigh-pressure nano-LC system for high-pH and low-pH RPLC separations in top-down proteomics. An online microtrap column with a dilution setup was used to collect eluted proteins from the first dimension high-pH separation and inject the fractions for ultrahigh-pressure long capillary column low-pH RPLC separation in the second dimension. This automatic platform enables the characterization of 1000+ intact proteoforms from 5 mu g of intact E. coli cell lysate in 10 online-collected fractions. Here, we have demonstrated that our online 2D pH RP/RPLC system coupled with top-down proteomics holds the potential for deep proteome characterization of mass-limited samples because it allows the identification of hundreds of intact proteoforms from complex biological samples at low microgram sample amounts.
引用
收藏
页码:12774 / 12777
页数:4
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