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'Shotgun' proteomic analyses without alkylation of cysteine

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Wisniewski,  Jacek R.
Mann, Matthias / Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Max Planck Society;

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Zettl,  Katharina
Mann, Matthias / Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Max Planck Society;

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Pilch,  Magdalena
Mann, Matthias / Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Max Planck Society;

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Rysiewicz,  Beata
Mann, Matthias / Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Max Planck Society;

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Sadok,  Ilona
Mann, Matthias / Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Max Planck Society;

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引用

Wisniewski, J. R., Zettl, K., Pilch, M., Rysiewicz, B., & Sadok, I. (2020). 'Shotgun' proteomic analyses without alkylation of cysteine. ANALYTICA CHIMICA ACTA, 1100, 131-137. doi:10.1016/j.aca.2019.12.007.


引用: https://hdl.handle.net/21.11116/0000-0005-E02D-C
要旨
It is a common belief that reduction of disulfide bridges and alkylation of thiols in proteins are indispensable steps in proteomic sample preparation. Since this chemical procedure is often incomplete and prone to side reactions we reexamined its importance. We found that reduction and alkylation do not increase the depth of analysis and quality of proteomic quantification and therefore these steps are not essential in 'shotgun'-type investigations of proteomes. Moreover, we found that compared to a standard procedure using iodoacetamide for thiol-alkylation, sample preparation under conditions protecting thiols from oxidation improves quality of peptides and allows identifying of 10-20% more peptides and proteins. Excluding thiol-alkylation from proteomic sample preparation shortens the workflows and decreases the probability of biases resulting from occurrence of artificially modified peptides. (C) 2020 Elsevier B.V. All rights reserved.