A highly efficient and automated method of purifying and desalting PCR products for analysis by electrospray ionization mass spectrometry

被引:71
作者
Jiang, Y [1 ]
Hofstadler, SA [1 ]
机构
[1] ISIS Pharmaceut, Ibis Therapeut Div, Carlsbad, CA 92008 USA
关键词
D O I
10.1016/S0003-2697(03)00024-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this work we present a rapid and fully automated method to purify and desalt PCR products prior to analysis by electrospray ionization mass spectrometry. The protocol employs a commercial pipette tip packed with an anion-exchange resin and comprises four primary steps: tip pretreatment, sample loading, rinsing, and sample elution. This tip-based purification/desalting protocol has two distinct advantages over previously published methods. First, the protocol can be performed either manually (1-12 samples at a time), using a standard p10 manual pipette, or in a fully automated microtiter plate format (96 samples at a time) employing standard laboratory robotics. Additionally, the entire protocol from crude PCR product to an "electrosprayable" analyte solution requires only 10 mul of crude product and takes less than 20 min. Using capillary gel electrophoresis, we demonstrate an overall recovery efficiency of similar to80% and demonstrate the exquisite desalting efficiency with high-performance electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry. Using an internal mass standard we demonstrate sub-ppm mass measurement error which provides an unambiguous base composition for a 120-mer PCR product. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:50 / 57
页数:8
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