Unknown

Dataset Information

0

H2-M3 restricted presentation of a Listeria-derived leader peptide.


ABSTRACT: Protective immunity to infection by many intracellular pathogens requires recognition by cytotoxic T lymphocytes (CTLs) of antigens presented on major histocompatibility complex (MHC) class I molecules. To be presented for recognition by pathogen-specific CTLs, these antigens must gain access to the host cell class I processing pathway. In the case of intracellular bacterial pathogens, the majority of bacterial proteins are retained within the bacterial membrane and therefore remain inaccessible to the host cell for antigen processing. We have isolated a CTL clone from a C57BL/6 mouse infected with the intracellular gram-positive bacterium Listeria monocytogenes (LM) and have identified the source of the antigen. Using a genomic expression library, we determined that the clone recognizes an antigenic N-formyl peptide presented by the nonpolymorphic murine MHC class Ib molecule, H2-M3. Several lengths of this peptide were able to sensitize cells for lysis by this CTL clone. The source of this antigenic peptide is a 23-amino acid polypeptide encoded at the start of a polycistronic region. Analysis of mRNA secondary structure of this region suggests that this polypeptide may be a leader peptide encoded by a transcriptional attenuator.

SUBMITTER: Princiotta MF 

PROVIDER: S-EPMC2212287 | biostudies-literature | 1998 May

REPOSITORIES: biostudies-literature

altmetric image

Publications

H2-M3 restricted presentation of a Listeria-derived leader peptide.

Princiotta M F MF   Lenz L L LL   Bevan M J MJ   Staerz U D UD  

The Journal of experimental medicine 19980501 10


Protective immunity to infection by many intracellular pathogens requires recognition by cytotoxic T lymphocytes (CTLs) of antigens presented on major histocompatibility complex (MHC) class I molecules. To be presented for recognition by pathogen-specific CTLs, these antigens must gain access to the host cell class I processing pathway. In the case of intracellular bacterial pathogens, the majority of bacterial proteins are retained within the bacterial membrane and therefore remain inaccessible  ...[more]

Similar Datasets

| S-EPMC2118191 | biostudies-literature
| S-EPMC3294130 | biostudies-literature
| S-EPMC3597455 | biostudies-literature
| S-EPMC3299774 | biostudies-literature
| S-EPMC3068915 | biostudies-other
| S-EPMC2118219 | biostudies-literature
| S-EPMC2193330 | biostudies-literature
| S-EPMC4512242 | biostudies-literature
| 2616404 | ecrin-mdr-crc
| S-EPMC7577990 | biostudies-literature