N1-0031 — Final report
1.
Fast profiling of protease specificity reveals similar substrate specificities for cathepsins K, L and S

In this article we report on a fast and simple approach for proteomic profiling of protease specificities (fast profiling of protease specificity (FPPS)), which can be applied to complex protein mixtures. FPPS is based on trideutero-acetylation of novel N-termini generated by the action of proteases and subsequent peptide fractionation on Stage Tips containing ion-exchange and reverse phase chromatographic resins. FPPS can be performed in 2 days and does not require extensive fractionation steps. Using this approach, we have determined the specificity profiles of the cysteine cathepsins K, L and S. We further validated our method by comparing the results with the specificity profiles obtained by the Nterminal combined fractional diagonal chromatography method.

COBISS.SI-ID: 28342823
2.
Current trends and challenges in proteomic identification of protease substrates

An overview of proteomic approaches used in protease research and were also applicable to the project.

COBISS.SI-ID: 29060647