| Literature DB >> 27862927 |
Min Zhu1, Pingbo Zhang2, Minghui Geng-Spyropoulos2, Ruin Moaddel1, Richard D Semba2, Luigi Ferrucci1.
Abstract
Selected reaction monitoring mass spectrometry (SRM-MS) is a sensitive and accurate method for the quantification of targeted proteins in biological specimens. However, the sample throughput and reliability of this technique is limited by the complexity of sample preparation, as well as instrumentation and data processing. Modern robotic equipment allows for rapid and accurate processing of large number of samples and makes SRM-MS assay applicable in epidemiological studies. Herein, we describe an automated sample processing platform developed in the context of an SRM-MS protocol for the assay of complement factor H protein and its variants in human plasma. We report detailed performance data on plasma digestion, sample cleanup and optimized robotic handling implemented on a Biomek® NXp Workstation. Method validation was assessed with isotopically labeled peptide standards and had high reproducibility of intra-day assay (CVs from 2.7 to 17.5% with median CV of 5.3%) and inter-day assay (CVs from 4.8 to 17.6 with median CV of 7.2%) for all peptides.Entities:
Keywords: Absolute quantification; Automated sample preparation; Heavy isotope-labeled peptides; Reproducibility; SRM; Technology
Mesh:
Year: 2016 PMID: 27862927 PMCID: PMC5534325 DOI: 10.1002/pmic.201600339
Source DB: PubMed Journal: Proteomics ISSN: 1615-9853 Impact factor: 3.984