Miniaturized and Automated High-Throughput Verification of Proteins in the ISET Platform with MALDI MS.

Summary, in English

A major bottleneck in high-throughput protein production is the validation step, which is why parallel and automated sample processing methods are highly desirable. Also, a miniaturized sample preparation format is preferred, as the reduction of reagent volumes significantly decreases the analysis cost per sample. We have developed an automated and miniaturized protein sequence verification protocol for recombinant proteins utilizing peptide mass fingerprinting and MS/MS analysis. The integrated selective enrichment target (ISET) platform, previously developed in our group, with its dual functionality, being both a sample preparation platform and a MALDI target plate, is employed. All steps including immobilized metal ion affinity chromatography of protein on cobalt-loaded beads, tryptic digestion, and MALDI MS analysis are performed in an array format, without any sample transfers, on the same ISET chip. The automated configuration reduced the sample preparation time significantly. Starting with crude lysate, a full plate of 48 purified, digested samples prepared for MALDI-MS can be generated in 4 h, with only 30 min of operator involvement. This paper demonstrates the utility of the method by parallel analysis of 45 His-tagged human recombinant proteins.

• Author: Belinda Adler; Tove Boström; Simon Ekström; Sophia Hober; Thomas Laurell
• Department/s: Department of Biomedical Engineering; MultiPark: Multidisciplinary research focused on Parkinson´s disease; BioCARE: Biomarkers in Cancer Medicine improving Health Care, Education and Innovation
• Publishing year: 2012
• Language: English
• Pages: 8663-8669
• Publication/Series: Analytical Chemistry
• Volume: 84
• Issue: 20
• Links: http://dx.doi.org/10.1021/ac3017983
• Document type: Journal article
• Publisher: The American Chemical Society (ACS)
• Topic: Analytical Chemistry
• Status: Published
• ISBN/ISSN/Other: ISSN: 1520-6882