4.6 Article

Performance comparison of three trypsin columns used in liquid chromatography

Journal

JOURNAL OF CHROMATOGRAPHY A
Volume 1490, Issue -, Pages 126-132

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.chroma.2017.02.024

Keywords

Digestion efficiency; Immobilized enzymatic reactor; Trypsin; Activity

Funding

  1. Agency of the Charles University in Prague [254214]
  2. Czech Science Foundation [16-05942S]
  3. National Institute of Health [5U24DK097153, 1R01DK101473-01A1]

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Trypsin is the most widely used enzyme in proteomic research due to its high specificity. Although the in solution digestion is predominantly used, it has several drawbacks, such as long digestion times, autolysis, and intolerance to high temperatures or organic solvents. To overcome these shortcomings trypsin was covalently immobilized on solid support and tested for its proteolytic activity. Trypsin was immobilized on bridge-ethyl hybrid silica sorbent with 300 (A) over circle pores, packed in 2.1 x 30mm column and compared with Perfinity and Poroszyme trypsin columns. Catalytic efficiency of enzymatic reactors was tested using N alpha-Benzoyl-L-arginine 4-nitroanilide hydrochloride as a substrate. The impact of buffer pH, mobile phase flow rate, and temperature on enzymatic activity was investigated. Digestion speed generally increased with the temperature from 20 to 37 degrees C. Digestion speed also increased with pH from 7.0 to 9.0; the activity of prototype enzyme reactor was highest at pH 9.0, when it activity exceeded both commercial reactors. Preliminary data for fast protein digestion are presented. (C) 2017 Elsevier B.V. All rights reserved.

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