Silicon microstructures for high-speed and high-sensitivity protein identifications

被引:37
作者
Laurell, T
Nilsson, J
Marko-Varga, G
机构
[1] AstraZeneca, Cell & Mol Biol, Res & Dev, S-22187 Lund, Sweden
[2] Univ Lund, Lund Inst Technol, Dept Elect Measurement, S-22100 Lund, Sweden
来源
JOURNAL OF CHROMATOGRAPHY B | 2001年 / 752卷 / 02期
基金
瑞典研究理事会;
关键词
silicon microstructures; proteins;
D O I
10.1016/S0378-4347(00)00358-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Silicon microtechnology has been used to develop a microstructure toolbox in order to enable high accuracy protein identification. During the last 2 years we developed and applied monocrystalline silicon structures and established new automated protein analysis platforms, The development of a high throughput protein platform is presented where fully automated protein identifications are performed. It includes the reduction and alkylation of the protein sample in a standard 96- or 384-well plate format prior to injection of 1 mul samples into the continuous flow based microtechnology platform. The processed sample is transferred to a microchip nanovial array target using piezoelectric microdispensing. identification is made by MALDI-TOF MS and a database search. After the initial sample reduction and alkylation period of 50 min the platform can digest and process protein samples at a speed of 100 samples in 210 min. An optional configuration of the platform, operating the dispenser in the 'static mode', enables on-target enrichment of low abundant proteins and peptides e.g. from 2DE samples. This makes detection at the low attomole level possible. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:217 / 232
页数:16
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