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Hypothesis-driven.
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Can identify reversible oxidation occupancy and type.
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Catalyst-free.
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Selective and bio-orthogonal.
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Internally normalised.
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Flexible—method can be readily adapted.
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Democratic—makes use of readily available equipment and techniques.
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Cost and time efficient.
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Suitable as an orthogonal workflow to redox proteomics.
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Could be useful for studying the redox state of hydrophobic and/or difficult to digest proteins.
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Investigator bias given hypothesis driven nature.
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Relies on the antibody recognising the PEGylated protein.
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Biophysical interaction between SDS and PEG.
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Careful PEG, antibody and gel size selection is required.
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May be difficult to study proteins with many solvent exposed thiols.
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Inability to use technique in certain species when available epitopes are not conserved.
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Multiple bands preclude multiplexing.
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