IDENTIFICATION OF NITRATION SITES ON SURFACTANT PROTEIN-A BY TANDEM ELECTROSPRAY MASS-SPECTROMETRY

Previous studies have shown that exposure of human surfactant protein A (SP-A) to nitrating agents [peroxynitrite (ONOO-); tetranitromethane (TNM; pH 8)] leads to nitrotyrosine formation. However, specific site s of nitration have not been identified. Herein, human SP-A, dissolved in Hepes buffer, was incubated with two boluses each of 0.5 mM ONOO- (pH 7.4) or 0.5 mM TNM (pH 8.0) for 15 min, After 30 min, SP-A samples were reduced, alkylated, and trypsin digested. The nitrated peptides and sites of amino acid nitration on the protein were identified by ca pillary high-performance liquid chromatography-coupled electrospray io nization tandem mass spectrometry (LC-ESMS/MS). The major nitrated pep tide on both TNM- and ONOO--exposed SP-A was the tryptic fragment Tyr( 161)-Arg(179) (YNTYAYVGLTEGPSPGDFR), located in the SP-A carbohydrate recognition domain. Sequencing of this nitrated peptide by LC-ESMS/MS demonstrated that the nitration was equally distributed on Tyr(164) an d Tyr(166). A second lesser nitrated peptide corresponding to tryptic fragment Asn(217)-Arg(222) (NCLYSR) was also found on TNM- and ONOO--m odified SP-A. No other nitrated amino acid was detected, Nitrated SP-A exhibited decreased ability to aggregate surfactant lipids in the pre sence of Ca2+. These data demonstrate that nitration of a specific tyr osine decreased an important protein function. (C) 1996 Academic Press , Inc.