Efficient MHC class I-independent amino-terminal trimming of epitope precursor peptides in the endoplasmic reticulum (Q40778984)

23 September 2017

title

Efficient MHC class I-independent amino-terminal trimming of epitope precursor peptides in the endoplasmic reticulum (English)

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23 September 2017

main subject

endoplasmic reticulum

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23 September 2017

D Fruci

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G Niedermann

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23 September 2017

R H Butler

series ordinal

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23 September 2017

language of work or name

English

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publication date

1 September 2001

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23 September 2017

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23 September 2017

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23 September 2017

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23 September 2017

page(s)

467-476

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Evidence that transporters associated with antigen processing translocate a major histocompatibility complex class I-binding peptide into the endoplasmic reticulum in an ATP-dependent manner

23 September 2017

cites work

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Interferon-gamma can stimulate post-proteasomal trimming of the N terminus of an antigenic peptide by inducing leucine aminopeptidase

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Structural characterization of a soluble and partially folded class I major histocompatibility heavy chain/beta 2m heterodimer

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The nature of the MHC class I peptide loading complex

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The human 26 S and 20 S proteasomes generate overlapping but different sets of peptide fragments from a model protein substrate

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A giant protease with potential to substitute for some functions of the proteasome

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The protease inhibitor, N-acetyl-L-leucyl-L-leucyl-leucyl-L-norleucinal, decreases the pool of major histocompatibility complex class I-binding peptides and inhibits peptide trimming in the endoplasmic reticulum

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Characterization of an incompletely assembled major histocompatibility class I molecule (H-2Kb) associated with unusually long peptides: implications for antigen processing and presentation

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The sizes of peptides generated from protein by mammalian 26 and 20 S proteasomes. Implications for understanding the degradative mechanism and antigen presentation

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Export of antigenic peptides from the endoplasmic reticulum intersects with retrograde protein translocation through the Sec61p channel

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7 January 2021

Human transporters associated with antigen processing (TAPs) select epitope precursor peptides for processing in the endoplasmic reticulum and presentation to T cells

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Proteolytic processing of peptides in the lumen of the endoplasmic reticulum for antigen presentation by major histocompatibility class I

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Cytotoxic T lymphocyte epitopes of HIV-1 Nef: Generation of multiple definitive major histocompatibility complex class I ligands by proteasomes

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Enhanced intracellular dissociation of major histocompatibility complex class I-associated peptides: a mechanism for optimizing the spectrum of cell surface-presented cytotoxic T lymphocyte epitopes.

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7 January 2021

Two novel routes of transporter associated with antigen processing (TAP)-independent major histocompatibility complex class I antigen processing

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7 January 2021

Two new proteases in the MHC class I processing pathway

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The peptide-binding motif for the human transporter associated with antigen processing

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HLA-A2 molecules in an antigen-processing mutant cell contain signal sequence-derived peptides

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7 January 2021

10.1016/S1074-7613(01)00203-5

Identifiers

DOI

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release_jbeiusffozdjhcxsy2jfq3m3ta

23 September 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/jbeiusffozdjhcxsy2jfq3m3ta

24 November 2022

mapped directly with Wikidata item

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