Issue 2, 2011

Phosphoproteome profile of human lung cancer cell line A549

Abstract

As an in vitro model for type II human lung cancer, A549 cells resist cytotoxicity via phosphorylation of proteins as demonstrated by many studies. However, to date, no large-scale phosphoproteome investigation has been conducted on A549. Here, we performed a systematical analysis of the phosphoproteome of A549 by using mass spectrometry (MS)-based strategies. This investigation led to the identification of 337 phosphorylation sites on 181 phosphoproteins. Among them, 67 phosphoproteins and 230 phosphorylation sites identified appeared to be novel with no previous characterization in lung cancer. Based on their known functions as reported in the literature, these phosphoproteins were functionally organized into highly interconnected networks. Western blotting and immunohistochemistry analyses were performed to validate the expression of a bottleneck phosphoprotein YAP1 in cancer cell lines and tissues. This dataset provides a valuable resource for further studies on phosphorylation and lung carcinogenesis.

Graphical abstract: Phosphoproteome profile of human lung cancer cell line A549

Supplementary files

Article information

Article type
Paper
Submitted
17 Jun 2010
Accepted
22 Sep 2010
First published
09 Nov 2010

Mol. BioSyst., 2011,7, 472-479

Phosphoproteome profile of human lung cancer cell line A549

G. Yu, C. Xiao, C. Lu, H. Jia, F. Ge, W. Wang, X. Yin, H. Jia, J. He and Q. He, Mol. BioSyst., 2011, 7, 472 DOI: 10.1039/C0MB00055H

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements