Evaluation of individual protein errors in silver-stained two-dimensional gels

被引:27
作者
Smales, CM [1 ]
Birch, JR
Racher, AJ
Marshall, CT
James, DC
机构
[1] Univ Kent, Res Sch Biosci, Canterbury CT2 7NJ, Kent, England
[2] Lonza Biol Plc, Slough SL1 4DY, Berks, England
[3] GlaxoSmithKline, Beckenham BR3 3BS, Kent, England
[4] Univ Queensland, Dept Chem Engn, Brisbane, Qld 4072, Australia
基金
英国生物技术与生命科学研究理事会;
关键词
2-DE quantitation; silver stain; NSO proteome; process error; mammalian cell culture; individual protein error;
D O I
10.1016/S0006-291X(03)01115-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The relationship between spot volume and variation for all protein spots observed on large format 2D gels when utilising silver stain technology and a model system based on mammalian NSO cell extracts is reported. By running multiple gels we have shown that the reproducibility of data generated in this way is dependent on individual protein spot volumes, which in turn are directly correlated with the coefficient of variation. The coefficients of variation across all observed protein spots were highest for low abundant proteins which are the primary contributors to process error, and lowest for more abundant proteins. Using the relationship between spot volume and coefficient of variation we show it is necessary to calculate variation for individual protein spot volumes. The inherent limitations of silver staining therefore mean that errors in individual protein spot volumes must be considered when assessing significant changes in protein spot volume and not global error. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:1050 / 1055
页数:6
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