Microscale phosphoproteome analysis of 10 000 cells from human cancer cell lines

Takeshi Masuda, Naoyuki Sugiyama, Masaru Tomita, Yasushi Ishihama

Research output: Contribution to journalArticlepeer-review

58 Citations (Scopus)

Abstract

We developed a miniaturized LC-MS system with a high-recovery phosphopeptide enrichment protocol that allows phosphoproteome analysis of 10 4 cells. In the enrichment protocol, the key step is to add sodium deoxycholate and sodium lauroyl sarcosinate to the buffer solution for protein extraction and digestion and to omit any subsequent desalt/desurfactant step before phosphopeptide enrichment. The phosphopeptides enriched by hydroxy acid-modified metal oxide chromatography (HAMMOC) are directly injected onto a miniaturized LC column using a nitrogen-pressure-driven cell, instead of switching valve-type injectors. The miniaturized analytical column of 25 μm diameter provided a 3.6-fold improvement in sensitivity over the conventional 100 μm diameter column. Overall, our analytical system provided approximately 80-fold improvement on average in the LC-MS response, and we identified 1011 unique phosphorylated sites based on 995 unique phosphopeptides from a single analysis of 10 4 HeLa cells (approximately 1 μg of proteins). This is the most sensitive phosphoproteomics system that has so far been reported for proteome-wide analysis of in vivo phosphorylation in mammalian cells.

Original languageEnglish
Pages (from-to)7698-7703
Number of pages6
JournalAnalytical chemistry
Volume83
Issue number20
DOIs
Publication statusPublished - 2011 Oct 15

ASJC Scopus subject areas

  • Analytical Chemistry

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