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磷酸化蛋白质组的定量动力学:细节决定成败。

Quantitative dynamics of phosphoproteome: the devil is in the details.

机构信息

T cell Signaling Laboratory, Sir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford, OX1 3RE, United Kingdom.

出版信息

Anal Chem. 2012 Oct 16;84(20):8431-6. doi: 10.1021/ac301833k. Epub 2012 Oct 4.

Abstract

Recent advances in peptide-based (bottom-up) quantitative proteomics and bioinformatics have opened unprecedented opportunities for extensive investigation of cellular proteomes and their dynamics. Here we discuss two approaches currently used to investigate the global dynamics of phosphorylation based on the isolation of phosphorylated proteins or peptides. We evaluate the accuracy of these methodologies to grasp the global dynamics of phosphorylation, and we raise awareness on ambiguities inherent to these analyses. We conclude that further development of targeted approaches should prevent inaccurate conclusions about the nature of biological regulations and in particular kinase-substrate networks.

摘要

近年来,基于肽段的(自下而上)定量蛋白质组学和生物信息学的进展为广泛研究细胞蛋白质组及其动态提供了前所未有的机会。在这里,我们讨论了两种目前用于研究基于磷酸化蛋白或肽段的磷酸化全局动态的方法。我们评估了这些方法学准确捕捉磷酸化全局动态的能力,并对这些分析中固有的模糊性提出了警示。我们的结论是,靶向方法的进一步发展应该可以避免对生物调控(尤其是激酶-底物网络)本质的不准确结论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08dd/3477822/1c56c3ad8edb/ac-2012-01833k_0005.jpg

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