4.8 Article

Development of an Online Microbore Hollow Fiber Enzyme Reactor Coupled with Nanoflow Liquid Chromatography-Tandem Mass Spectrometry for Global Proteomics

Journal

ANALYTICAL CHEMISTRY
Volume 85, Issue 11, Pages 5506-5513

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ac400625k

Keywords

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Funding

  1. Converging Research Center Program through the National Research Foundation of Korea (NRF)
  2. Ministry of Education, Science and Technology [2011K000890]
  3. KRISS
  4. [NRF-2010-0014046]

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In this study, we report the development of a microbore hollow fiber enzyme reactor (mHFER) coupled to nanoflow liquid chromatography-tandem mass, spectrometry (nLC-ESI-MS/MS) for the online digestion or selective enrichment of glycopeptides and analysis of proteins. With mHFER, enzymatic digestion of protein could be achieved by continuous flow within a very small volume (-10 mu L) of mHF inserted in a PEEK tube. Digested peptides exited through the pores of the hollow, fiber membrane wall to external single or multiplexed trap columns for nLC-ESI-MS/MS analysis. Evaluation of online mHFER, -nLC-ESI-Mg/MS system was made with bovine, serum albumin,(B varying SA) by varying the temperature of digestion and the amount of protein injected. We evaluated the ability of the mHFER system to enrich glycopeptides by injecting a and digested peptides from alpha-1-acid glycoprotein (AGP) into the mHFER, followed by, delivery of PNGase F for endoglycosidic digestion Nonglycosylated peptides unbound to lectins eluted at the first breakthrough run while N-linked glycopeptides eluted after the endoglycosidic digestion. the developed method was applied to urine samples from patients with prosatate cancer and controls, endoglycosidic digestion. The developed method was applied to urine samples from Patients with Prostate cancer and controls; 67 N-linked glycopeptides were identified and relative differences in glycopeptide content between patient and control samples were determined.

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