Single-molecule site-specific detection of protein phosphorylation with a nanopore.

Rosen CB, Rodriguez-Larrea D, Bayley H

We demonstrate single-molecule, site-specific detection of protein phosphorylation with protein nanopore technology. A model protein, thioredoxin, was phosphorylated at two adjacent sites. Analysis of the ionic current amplitude and noise, as the protein unfolds and moves through an α-hemolysin pore, enables the distinction between unphosphorylated, monophosphorylated and diphosphorylated variants. Our results provide a step toward nanopore proteomics.

Keywords:

Amino Acid Sequence

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Biotechnology

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Models, Molecular

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Molecular Sequence Data

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Nanopores

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Phosphorylation

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Proteins

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Proteomics

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Sequence Alignment