Screening for protein phosphorylation using nanoscale reactions on microdroplet arrays

Journal Article (2015)
Authors

Simon Karl Küster (ETH Zürich)

Martin Pabst (ETH Zürich)

Renato Zenobi (ETH Zürich)

Petra S. Dittrich (ETH Zürich)

Affiliation
External organisation
To reference this document use:
https://doi.org/10.1002/anie.201409440
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Publication Year
2015
Language
English
Affiliation
External organisation
Issue number
5
Volume number
54
Pages (from-to)
1671-1675
DOI:
https://doi.org/10.1002/anie.201409440

Abstract

We present a novel and straightforward screening method to detect protein phosphorylations in complex protein mixtures. A proteolytic digest is separated by a conventional nanoscale liquid chromatography (nano-LC) separation and the eluate is immediately compartmentalized into microdroplets, which are spotted on a microarray MALDI plate. Subsequently, the enzyme alkaline phosphatase is applied to every second microarray spot to remove the phosphate groups from phosphorylated peptides, which results in a mass shift of nx - 80 Da. The MALDI-MS scan of the microarray is then evaluated by a software algorithm to automatically identify the phosphorylated peptides by exploiting the characteristic chromatographic peak profile induced by the phosphatase treatment. This screening method does not require extensive MS/MS experiments or peak list evaluation and can be easily extended to other enzymatic or chemical reactions.

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