iPhos: toolkit to streamline the alkaline phosphatase assisted comprehensive LC-MS phosphoproteome investigation — ASN Events

iPhos: toolkit to streamline the alkaline phosphatase assisted comprehensive LC-MS phosphoproteome investigation (#33)

Tzu-Hsien Yang 1 , Hong-Tsun Chang 1 , Eric S.L. Hsiao 2 , Juo-Ling Sun 2 , Chung-Ching Wang 1 , Hsin-Yi Wu 3 , Pao-Chi Liao 2 , Wei-Sheng Wu 1
  1. Department of Electrical Engineering , National Cheng Kung University, Tainan, Taiwan
  2. Department of Environmental and Occupational Health, National Cheng Kung University, Tainan, Taiwan
  3. Institute of Chemistry, Academia Sinica, Taipei, Taiwan
Comprehensive characterization of the phosphoproteome in living cells is critical in signal transduction research. But the low abundance of phosphopeptides among the total proteome in cells remains an obstacle in mass spectrometry-based proteomic analysis. To provide a solution, an alternative analytic strategy to confidently identify phosphorylated peptides by using the alkaline phosphatase (AP) treatment combined with high-resolution mass spectrometry was provided. While the process is applicable, the key integration along the pipeline was mostly done by tedious manual work.

We developed a software toolkit, iPhos, to facilitate and streamline the work-flow of AP-assisted phosphoproteome characterization. The iPhos tookit includes one assister and three modules. The iPhos Peak Extraction Assister automates the batch mode peak extraction for multiple liquid chromatography mass spectrometry (LC-MS) runs. iPhos Module-1 can process the peak lists extracted from the LC-MS analyses derived from the original and dephosphorylated samples to mine out potential phosphorylated peptide signals based on mass shift caused by the loss of some multiples of phosphate groups. iPhos Module-2 provides customized inclusion lists with peak retention time windows for subsequent targeted LC-MS/MS experiments. iPhos Module-3 facilitates to link the peptide identifications from protein search engines with the quantification results from pattern-based label-free quantification tools. We further demonstrated the utility of the iPhos toolkit on the data of human metastatic lung cancer cells (CL1-5).

In the comparison study of the control group of CL1-5 cell lysates and the treatment group of datasinib-treated CL1-5 cell lysates, we demonstrated the applicability of the iPhos toolkit and reported the experimental results based on the iPhos-facilitated phosphoproteome investigation. We also compared the strategy with pure DDA-based LC-MS/MS phosphoproteome investigation. The results of iPhos-facilitated targeted LC-MS/MS convey more thorough and confident phosphopeptide identification than the results of pure DDA LC-MS/MS. The iPhos software toolkit and sample tutorial data are available at http://cosbi3.ee.ncku.edu.tw/iPhos/.