Fig. 1From: Optimization of quantitative proteomic analysis of clots generated from plasma of patients with venous thromboembolismEfficiency of protein to peptide conversion after digestion with LysC, trypsin and chymotrypsin. The yields were expressed as a ratio of the amount of eluted peptides to total protein amount processed (a). The number of unique peptides identified after sequential digestion with LysC (L), LysC + trypsin (L + T), LysC + trypsin + chymotrypsin (L + T + CT) or peptide fractionation by pipet-tip strong anion exchange (SAX) protocol (b). The number of proteins identified after sequential digestion with L, L + T, L + T + CT or peptide fractionation by SAX (c). Sequence coverage obtained after sequential digestion with L, L + T, L + T + CT or peptide fractionation by SAX for three different proteins: fibrinogen gamma chain, coagulation factor XIII a and antithrombin-III (d). *p < 0.05 as compared to L, # p < 0.05 as compared to L + T, † p < 0.05 as compared to L + T + CT; mean ± SEM; n = 4 per groupBack to article page