We report the development of a 96-well plate proteomic reactor for gel-free processing of minute amounts of complex proteomic samples. The device performs multiplexed trapping, enrichment, and biochemical processing of proteins, resulting in concentrated peptide solutions ready for mass spectrometric analysis. Individual wells on the reactor can process up to 2 μg of protein. We also report the coupling of the plate proteomic reactor with protein fractionation using size-exclusion chromatography for large-scale identification of proteins. To illustrate the potential of this approach, we separated 400 μg of MCF7 cell lysate using size-exclusion chromatography and processed 35 protein fractions on the reactor plate. Using stringent criteria when searching the data, a total of 875 unique proteins were identified. More relaxed searching conditions associated with a 1% false positive rate led to the identification of 2683 unique proteins, meaning that one protein was identified per 3-10 ng of total protein lysate loaded on the reactor plate.

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Persistent URL dx.doi.org/10.1021/ac061248v
Journal Analytical Chemistry
Hou, W. (Weimin), Ethier, M. (Martin), Smith, J. C, Sheng, Y. (Yinglun), & Figeys, D. (Daniel). (2007). Multiplexed proteomic reactor for the processing of proteomic samples. Analytical Chemistry, 79(1), 39–44. doi:10.1021/ac061248v