Picoelectrospray Ionization Mass Spectrometry Using Narrow-Bore Chemically Etched Emitters

被引:54
作者
Marginean, Ioan [1 ]
Tang, Keqi [1 ]
Smith, Richard D. [1 ]
Kelly, Ryan T. [2 ]
机构
[1] Pacific NW Natl Lab, Div Biol Sci, Richland, WA 99352 USA
[2] Pacific NW Natl Lab, Environm Mol Sci Lab, Richland, WA 99352 USA
基金
美国国家卫生研究院;
关键词
Nanoelectrospray; nano-ESI; Quantitation; Mass-limited analysis; CAPILLARY-ZONE-ELECTROPHORESIS; HIGH-SENSITIVITY ANALYSIS; SINGLE-CELL ANALYSIS; ELECTROSPRAY-IONIZATION; LIQUID-CHROMATOGRAPHY; ION-SPRAY; NANOELECTROSPRAY IONIZATION; NANOFLOW REGIME; DYNAMIC-RANGE; BEVELED EDGE;
D O I
10.1007/s13361-013-0749-z
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Electrospray ionization mass spectrometry (ESI-MS) at flow rates below similar to 10 nL/min has been only sporadically explored because of difficulty in reproducibly fabricating emitters that can operate at lower flow rates. Here we demonstrate narrow orifice chemically etched emitters for stable electrospray at flow rates as low as 400 pL/min. Depending on the analyte concentration, we observe two types of MS signal response as a function of flow rate. At low concentrations, an optimum flow rate is observed slightly above 1 nL/min, whereas the signal decreases monotonically with decreasing flow rates at higher concentrations. For example, consumption of 500 zmol of sample yielded signal-to-noise ratios similar to 10 for some peptides. In spite of lower MS signal, the ion utilization efficiency increases exponentially with decreasing flow rate in all cases. Significant variations in ionization efficiency were observed within this flow rate range for an equimolar mixture of peptide, indicating that ionization efficiency is an analyte-dependent characteristic for the present experimental conditions. Mass-limited samples benefit strongly from the use of low flow rates and avoiding unnecessary sample dilution. These findings have important implications for the analysis of trace biological samples.
引用
收藏
页码:30 / 36
页数:7
相关论文
共 48 条
[1]   High sensitivity analysis of neutral underivatized oligosaccharides by nanoelectrospray mass spectrometry [J].
Bahr, U ;
Pfenninger, A ;
Karas, M ;
Stahl, B .
ANALYTICAL CHEMISTRY, 1997, 69 (22) :4530-4535
[2]  
Bateman KP, 1997, RAPID COMMUN MASS SP, V11, P307
[3]   A new sheathless electrospray interface for coupling of capillary electrophoresis to ion-trap mass spectrometry [J].
Bendahl, L ;
Hansen, SH ;
Olsen, J .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2002, 16 (24) :2333-2340
[4]   Chip-based nanoflow high performance liquid chromatography coupled to mass spectrometry for profiling of soybean flavonoids [J].
Chang, Yuwei ;
Zhao, Chunxia ;
Wu, Zeming ;
Zhou, Jia ;
Zhao, Sumin ;
Lu, Xin ;
Xu, Guowang .
ELECTROPHORESIS, 2012, 33 (15) :2399-2406
[5]   Sheathless capillary electrophoresis/electrospray mass spectrometry using a carbon-coated tapered fused-silica capillary with a beveled edge [J].
Chang, YZ ;
Chen, YR ;
Her, GR .
ANALYTICAL CHEMISTRY, 2001, 73 (21) :5083-5087
[6]   Design and performance of a low-flow capillary electrophoresis-electrospray-mass spectrometry interface using an emitter with dual beveled edge [J].
Chen, YR ;
Tseng, MC ;
Her, GR .
ELECTROPHORESIS, 2005, 26 (7-8) :1376-1382
[7]   A simple method for fabrication of silver-coated sheathless electrospray emitters [J].
Chen, YR ;
Her, GR .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2003, 17 (05) :437-441
[8]   A MICROSCALE ELECTROSPRAY INTERFACE FOR ONLINE, CAPILLARY LIQUID-CHROMATOGRAPHY TANDEM MASS-SPECTROMETRY OF COMPLEX PEPTIDE MIXTURES [J].
DAVIS, MT ;
STAHL, DC ;
HEFTA, SA ;
LEE, TD .
ANALYTICAL CHEMISTRY, 1995, 67 (24) :4549-4556
[9]   Efficiency of nano-electrospray ionization [J].
El-Faramawy, A ;
Siu, KWM ;
Thomson, BA .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 2005, 16 (10) :1702-1707
[10]   MICRO-ELECTROSPRAY MASS-SPECTROMETRY - ULTRA-HIGH-SENSITIVITY ANALYSIS OF PEPTIDES AND PROTEINS [J].
EMMETT, MR ;
CAPRIOLI, RM .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1994, 5 (07) :605-613