Proteomics

Dataset Information

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‘Shotgun’ Proteome Analyses Do Not Require Alkylation of Cysteine


ABSTRACT: 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 and can results in various artefacts we reexamined its importance. We found that the reduction and alkylation do not increase the depth of analysis and quality of proteomic quantification therefore these steps are unessential 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 the thiol-alkylation from proteomic sample preparation, shorten the workflows, and decreases the probability of biases resulting from occurrence of artificially modified peptides.

INSTRUMENT(S): LTQ Orbitrap, Q Exactive

ORGANISM(S): Homo Sapiens (human) Mus Musculus (mouse)

TISSUE(S): Brain, Liver, Cell Culture

SUBMITTER: Jacek Wisniewski  

LAB HEAD: Jacek R Wisniewski

PROVIDER: PXD014000 | Pride | 2020-01-21

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
20160812_QEp7_JRW_SA_L_T77.raw Raw
20160812_QEp7_JRW_SA_L_T78.raw Raw
20160812_QEp7_JRW_SA_L_T79.raw Raw
20160812_QEp7_JRW_SA_L_T80.raw Raw
20160812_QEp7_JRW_SA_L_T81.raw Raw
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Publications

'Shotgun' proteomic analyses without alkylation of cysteine.

Wiśniewski Jacek R JR   Zettl Katharina K   Pilch Magdalena M   Rysiewicz Beata B   Sadok Ilona I  

Analytica chimica acta 20191204


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  ...[more]

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