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Title: Fatty acylation of murine Ia alpha, beta and invariant chains

Conference · · Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States)
OSTI ID:7024701

Post-translational modification of MHC Class II molecules may influence their subsequent fate in further post-translational processing or in cell trafficking and expression in a recognizable form at the cell surface. Radiolabelling of lymphoid cells with (/sup 3/H)-palmitate permits the detection of covalently linked fatty acid chains on Ia alpha and beta glycopeptides and on the invariant chain (Ii). The attached fatty acid is stable to SDS-polyacrylamide gel electrophoresis, and is released in a chloroform/methanol extractable form by reagents which disrupt ester linkages. Fatty acid linkages to alpha and beta chains are sensitive to alkaline hydrolysis in KOH/methanol, and are therefore identified as hydroxyesters. The fatty acid linkage to invariant chain is susceptible to mild neutral hydrolysis in hydroxylamine or KOH/methanol, and this lability indicates that it is a thioester. Mobility of released radiolabelled material in thin layer chromatography verifies that the radiolabel remains in fatty acid. Fatty acylation has been noted in I-A and I-E molecules from all MHC haplotypes tested. Class I molecules were also found to be fatty acylated. None of the fatty acid linkages were of the amide type.

Research Organization:
Washington Univ. School of Medicine, St. Louis, MO
OSTI ID:
7024701
Report Number(s):
CONF-8604222-
Journal Information:
Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States), Vol. 45:4; Conference: 70. annual meeting of the Federation of American Society for Experimental Biology, St. Louis, MO, USA, 13 Apr 1986
Country of Publication:
United States
Language:
English