The myeloperoxidase system of human phagocytes generates N^ε-(carboxymethyl)lysine on proteins: a mechanism for producing advanced glycation end products at sites of inflammation
J. Clin. Invest. Melissa M. Anderson, et al. 104:103 doi:10.1172/JCI3042 [Go to this article.]

Figure 1
Progress curve of protein browning induced by the HOCl-serine system. HOCl and L-serine (0.9:1.0 mol/mol at the indicated final concentration) were incubated together in buffer A (50 mM sodium phosphate buffer [pH 7.0]) for 15 minutes at 37°C. RNase A (100 mg/mL in buffer A) was then added to a final concentration of 10 mg/mL, and the absorbance at 325 nm of the reaction mixture was monitored. When indicated, 20 mM NaCNBH₃ was present during the reaction of HOCl and L-serine.