Burster, unpublished data). We note that a dihistidine motif is adjacent to the CatG cleavage site of MHC II molecules (Fig. 4a), which might regulate CatG access in a pH-dependent fashion. However, GW-572016 nmr the pH dependence does not explain why even high concentrations of CatG
added to B-LCLs at neutral pH failed to cleave DR molecules at the cell surface. The simplest interpretation of the latter result is that the CatG cleavage site of MHC II molecules is sterically inaccessible when the MHC II molecules are embedded in endosomal or cell surface membranes. The steric hindrance could, in principle, come from the proximity of the membrane itself, or from noncovalent associations with other proteins, both of which would be disrupted by detergent lysis. Partial steric masking may also explain why, in most experiments,
full-length DR embedded in detergent micelles was digested less completely than soluble recombinant DR ectodomains. Our results do not prove that CatG is never involved in MHC II degradation in vivo. For instance, CatG might conceivably act on MHC II molecules that have partially lost their native conformation at the end of their useful life. However, our findings do suggest that MHC II molecules have evolved resistance to endosomal proteolysis by a combination of mechanisms. The inherent resistance of MHC II ectodomains to many cathepsins is likely to be important. Other protease cleavage sites, such as the CatG cleavage site studied here, may be cryptic, either Depsipeptide because of charge characteristics that impair proteolytic learn more attack in acidic endosomal compartments, or because they are sterically inaccessible at APC membranes, or both. Steric inaccessibility of the CatG cleavage site may be particularly important in allowing antigen presentation to be maintained
in inflamed tissues, in which CatG is abundantly released into the extracellular space by activated neutrophils. Whether cryptic protease cleavage sites contribute to regulated turnover of MHC II molecules remains to be determined. This work was supported by grants from the Deutsche Forschungsgemeinschaft (DFG; BU1822/1-1) to TB, SFB 518, GRK 1041-2, and Else Kröner-Fresensius-Stiftung to BOB, funding from Sidney Sussex College and the Arthritis Research Campaign (ref. 18543) to RB, and grants from the NIH and the Child Health Research Program (Stanford University) to EDM. We gratefully acknowledge A. Guzzetta for mass spectrometry and L. Stern for providing HLA-DR1 molecules made in E. coli and the CHAMP anti-DR antisera. Other purified MHC II molecules, HLA-DR2b, murine I-Ag7 and I-Ek, were kindly provided by K. Wucherpfennig, L. Teyton and M. Davis, respectively. CatG−/− mice were kindly provided by C. Pham. The authors do not have any conflicting interests. Data S1. Sequential digest of HLA-DR3. Data S2.