Literature DB >> 1538129

pH dependence of the interaction between immunogenic peptides and MHC class II molecules. Evidence for an acidic intracellular compartment being the organelle of interaction.

S Mouritsen1, A S Hansen, B L Petersen, S Buus.   

Abstract

The pH dependence of the interaction between immunogenic peptide and MHC class II was studied both in a direct biochemical binding assay and in a functional Ag presentation assay. The two approaches yielded similar results. All of the peptides tested bound optimally to their relevant MHC class II restriction element at around pH 4.5. Indeed, several of the peptides did not bind at neutral pH. These results demonstrate that Ag under physiologic conditions meet MHC class II in a quite acidic environment. The very acidic pH optimal for peptide-MHC class II interaction is only found intracellularly and most notably in the endosome-lysosome compartment in which Ag processing is thought to occur. Thus, Ag processing and interaction with MHC class II molecules can potentially happen in the very same compartment. This yet undefined acidic compartment would have to contain proteolytic enzymes and MHC class II molecules.

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Year:  1992        PMID: 1538129

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  8 in total

1.  MHC class II-bound self-peptides can be effectively separated by isoelectric focusing and bind optimally to their MHC class II restriction elements around pH 5.0.

Authors:  S Mouritsen; I Dalum; A M Engel; I M Svane; I Svendsen; O Werdelin; H Elsner
Journal:  Immunology       Date:  1994-08       Impact factor: 7.397

2.  Binding of gluten-derived peptides to the HLA-DQ2 (alpha1*0501, beta1*0201) molecule, assessed in a cellular assay.

Authors:  R G Shidrawi; N D Parnell; P J Ciclitira; P Travers; G Evan; S Rosen-Bronson
Journal:  Clin Exp Immunol       Date:  1998-01       Impact factor: 4.330

3.  A structural transition in class II major histocompatibility complex proteins at mildly acidic pH.

Authors:  H A Runnels; J C Moore; P E Jensen
Journal:  J Exp Med       Date:  1996-01-01       Impact factor: 14.307

4.  Selective release of some invariant chain-derived peptides from HLA-DR1 molecules at endosomal pH.

Authors:  R G Urban; R M Chicz; J L Strominger
Journal:  J Exp Med       Date:  1994-08-01       Impact factor: 14.307

5.  Membrane interactions influence the peptide binding behavior of DR1.

Authors:  M A Sherman; H A Runnels; J C Moore; L J Stern; P E Jensen
Journal:  J Exp Med       Date:  1994-01-01       Impact factor: 14.307

6.  T cell responses affected by aminopeptidase N (CD13)-mediated trimming of major histocompatibility complex class II-bound peptides.

Authors:  S L Larsen; L O Pedersen; S Buus; A Stryhn
Journal:  J Exp Med       Date:  1996-07-01       Impact factor: 14.307

7.  Evidence for a conformational change in a class II major histocompatibility complex molecule occurring in the same pH range where antigen binding is enhanced.

Authors:  J J Boniface; D S Lyons; D A Wettstein; N L Allbritton; M M Davis
Journal:  J Exp Med       Date:  1996-01-01       Impact factor: 14.307

8.  Myocarditis-inducing epitope of myosin binds constitutively and stably to I-Ak on antigen-presenting cells in the heart.

Authors:  D L Donermeyer; K W Beisel; P M Allen; S C Smith
Journal:  J Exp Med       Date:  1995-11-01       Impact factor: 14.307

  8 in total

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