Stable Isotope N-Phosphorylation Labeling for Peptide de Novo Sequencing and Protein Quantification Based on Organic Phosphorus Chemistry

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	Stable Isotope N-Phosphorylation Labeling for Peptide de Novo Sequencing and Protein Quantification Based on Organic Phosphorus Chemistry
	Gao, Xiang ; Wu, Hanzhi ; Lee, Kim-Chung ; Liu, Hongxia ; Zhao, Yufen ; Cai, Zongwei ; Jiang, Yuyang ; Zhao YF(赵玉芬)
刊名	http://dx.doi.org/10.1021/ac301939v
	2012-12-04
关键词	IONIZATION MASS-SPECTROMETRY QUANTITATIVE PROTEOMICS AMINO-ACIDS ISOBARIC TAGS CELL-CULTURE AFFINITY TAG SILAC DERIVATIZATION STRATEGY MIXTURES
英文摘要	National Natural Science Foundation of China [20928005, 21172129]; Ministry of Science and Technology of China [2011DFA30620]; In this paper, we describe the development of a novel stable isotope N-phosphorylation labeling (SIPL) strategy for peptide de novo sequencing and protein quantification based on organic phosphorus chemistry. The labeling reaction could be performed easily and completed within 40 min in a one-pot reaction without additional cleanup procedures. It was found that N-phosphorylation labeling reagents were activated in situ to form labeling intermediates with high reactivity targeting on N-terminus and epsilon-amino groups of lysine under mild reaction conditions. The introduction of N-terminal-labeled phosphoryl group not only improved the ionization efficiency of peptides and increased the protein sequence coverage for peptide mass fingerprints but also greatly enhanced the intensities of b ions, suppressed the internal fragments, and reduced the complexity of the tandem mass spectrometry (MS/MS) fragmentation patterns of peptides. By using nano liquid chromatography chip/time-of-flight mass spectrometry (nano LC-chip/TOF MS) for the protein quantification, the obtained results showed excellent correlation of the measured ratios to theoretical ratios with relative errors ranging from 0.5% to 6.7% and relative standard deviation of less than 10.6%, indicating that the developed method was reproducible and precise. The isotope effect was negligible because of the deuterium atoms were placed adjacent to the neutral phosphoryl group with high electrophilicity and moderately small size. Moreover, the SIPL approach used inexpensive reagents and was amenable to samples from various sources, including cell culture, biological fluids, and tissues. The method development based on organic phosphorus chemistry offered a new approach for quantitative proteomics by using novel stable isotope labeling reagents.
语种	英语
内容类型	期刊论文
源URL	[http://dspace.xmu.edu.cn/handle/2288/63606]
专题	化学化工－已发表论文
推荐引用方式 GB/T 7714	Gao, Xiang,Wu, Hanzhi,Lee, Kim-Chung,et al. Stable Isotope N-Phosphorylation Labeling for Peptide de Novo Sequencing and Protein Quantification Based on Organic Phosphorus Chemistry[J]. http://dx.doi.org/10.1021/ac301939v,2012.
APA	Gao, Xiang.,Wu, Hanzhi.,Lee, Kim-Chung.,Liu, Hongxia.,Zhao, Yufen.,...&赵玉芬.(2012).Stable Isotope N-Phosphorylation Labeling for Peptide de Novo Sequencing and Protein Quantification Based on Organic Phosphorus Chemistry.http://dx.doi.org/10.1021/ac301939v.
MLA	Gao, Xiang,et al."Stable Isotope N-Phosphorylation Labeling for Peptide de Novo Sequencing and Protein Quantification Based on Organic Phosphorus Chemistry".http://dx.doi.org/10.1021/ac301939v (2012).