4.6 Article

On-target titanium dioxide-based enrichment for characterization of phosphorylations in the Adenovirus pIIIa protein

期刊

JOURNAL OF CHROMATOGRAPHY A
卷 1317, 期 -, 页码 105-109

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.chroma.2013.08.096

关键词

Phosphopeptide enrichment; MALDI-MS; Separation; Capsid protein precursor pills; TiO2

资金

  1. Swedish Research Council
  2. P.O. Zetterling foundation
  3. A. Wiberg foundation

向作者/读者索取更多资源

A recently developed titanium dioxide (TiO2) based on-target method for phosphopeptide enrichment and matrix assisted laser desorption-ionization mass spectrometry (MALDI MS) analysis was used to investigate phosphorylations in the Adenovirus type 2 structural protein pIIIa. Lysates of purified virus particles were separated on 1-D SDS-PAGE and the band for the pIIIa protein was excised for tryptic digestion into peptides that were enriched with the on-target method. The enrichment provided by the method clearly improved the detectability of phosphorylated peptides and the results show for the first time evidence for multi-phosphorylated peptides in pIIIa. Moreover, three novel phosphorylations were identified in the protein sequence, even though the precise positions could not be determined. These results illustrate the potential of the method for the characterization of novel phosphoproteomes in biological samples of medical relevance. (C) 2013 Elsevier B.V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据