Abstract
The use of two different monoliths located in capillaries for on-line protein digestion, preconcentration of peptides and their separation has been demonstrated. The first monolith was used as support for covalent immobilization of pepsin. This monolith with well-defined porous properties was prepared by in situ copolymerization of 2-vinyl-4,4-dimethylazlactone and ethylene dimethacrylate. The second, poly(lauryl methacrylate-co-ethylene dimethacrylate) monolith with a different porous structure served for the preconcentration of peptides from the digest and their separation in reversed-phase liquid chromatography mode. The top of the separation capillary was used as a preconcentrator, thus enabling the digestion of very dilute solutions of proteins in the bioreactor and increasing the sensitivity of the mass spectrometric detection of the peptides using a time-of-flight mass spectrometer with electrospray ionization. Myoglobin, albumin, and hemoglobin were digested to demonstrate feasibility of the concept of using the two monoliths in-line. Successive protein injections confirmed both the repeatability of the results and the ability to reuse the bioreactor for at least 20 digestions.
Original language | English (US) |
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Pages (from-to) | 88-96 |
Number of pages | 9 |
Journal | Journal of Chromatography A |
Volume | 1188 |
Issue number | 2 |
DOIs | |
State | Published - Apr 25 2008 |
Externally published | Yes |
Keywords
- Enzymatic reactor
- Immobilized enzyme
- Mass spectrometry
- Monolithic columns
- NanoHPLC
- Pepsin
ASJC Scopus subject areas
- Analytical Chemistry
- Biochemistry
- Organic Chemistry