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Rapid sample processing for LC-MS-based quantitative proteomics using high intensity focused ultrasound.


ABSTRACT: A new sample processing workflow that uses high intensity focused ultrasound to rapidly reduce and alkylate cysteines, digest proteins and then label peptides with (18)O was developed for quantitative proteomics applications. Each step was individually refined to minimize reaction times, peptide loses and undesired byproducts or modifications. When this novel workflow was used, mouse plasma proteins were successfully denatured, alkylated, in-solution digested, and (18)O-labeled in <10 min for subsequent analysis by liquid chromatography-electrospray ionization high resolution mass spectrometry. Performance was evaluated in terms of the number of mouse plasma peptides and proteins identified in a shotgun approach and the quantitative dynamic range. The results were compared with previously published results obtained using conventional sample preparation methods and were found to be similar. Advantages of the new method include greatly simplified and accelerated sample processing, as well as being readily amenable to automation.

SUBMITTER: Lopez-Ferrer D 

PROVIDER: S-EPMC2744207 | biostudies-literature | 2008 Sep

REPOSITORIES: biostudies-literature

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Rapid sample processing for LC-MS-based quantitative proteomics using high intensity focused ultrasound.

López-Ferrer Daniel D   Heibeck Tyler H TH   Petritis Konstantinos K   Hixson Kim K KK   Qian Weijun W   Monroe Matthew E ME   Mayampurath Anoop A   Moore Ronald J RJ   Belov Mikhail E ME   Camp David G DG   Smith Richard D RD  

Journal of proteome research 20080808 9


A new sample processing workflow that uses high intensity focused ultrasound to rapidly reduce and alkylate cysteines, digest proteins and then label peptides with (18)O was developed for quantitative proteomics applications. Each step was individually refined to minimize reaction times, peptide loses and undesired byproducts or modifications. When this novel workflow was used, mouse plasma proteins were successfully denatured, alkylated, in-solution digested, and (18)O-labeled in <10 min for su  ...[more]

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