Rapid and efficient proteolysis through laser-assisted immobilized enzyme reactors

► The near-IR laser radiation can accelerate the proteolysis efficiency through IMER significantly. ► The whole process can be completed in 1 min and room temperature. ► Satisfying analysis of human serum sample using laser-assisted IMER proteolysis. In this report, laser radiation (808 nm) for the...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of Chromatography A 2011-11, Vol.1218 (47), p.8567-8571
Hauptverfasser: Zhang, Peng, Gao, Mingxia, Zhu, Shaochun, Lei, Jie, Zhang, Xiangmin
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:► The near-IR laser radiation can accelerate the proteolysis efficiency through IMER significantly. ► The whole process can be completed in 1 min and room temperature. ► Satisfying analysis of human serum sample using laser-assisted IMER proteolysis. In this report, laser radiation (808 nm) for the first time was employed to enhance the efficiency of proteolysis through immobilized enzyme reactor (IMER). IMER based monolithic support was prepared in the fused-silica capillary via a simple two-step procedure including acryloylation on trypsin surface and in situ aqueous polymerization/immobilization. The feasibility and high efficiency of the laser-assisted IMER were demonstrated by the digestion of bovine serum albumin (BSA), cytochrome c (Cyt-c) and β-casein. The digestion process was achieved in 60 s. The peptides were identified by MALDI-TOF-MS, yielding the sequence coverage of 33% for BSA, 73% for Cyt-c and 22% for β-casein. The comparisons between the in-solution digestion and on IMER reaction with/without laser assistance were made. To further confirm its efficiency in proteome analysis, the laser-assisted IMER was also applied to the analysis of one fraction of human serum sample through two-dimensional (2-D) separation of strong anion exchange/reversed-phase liquid chromatography (SAX/RPLC). After a database search, 49 unique peptides corresponding to 5 proteins were identified. The results showed that the laser-assisted IMER provides a promising platform for the high-throughput protein identification.
ISSN:0021-9673
1873-3778
DOI:10.1016/j.chroma.2011.09.084