ERAP Inhibitors in Autoimmunity and Immuno-Oncology: Medicinal Chemistry Insights-Reference-Cited by-同舟云学术

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ERAP Inhibitors in Autoimmunity and Immuno-Oncology: Medicinal Chemistry Insights

Published:2024-07-16 Issue:14 Volume:67 Page:11597-11621
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Fougiaxis Vasileios¹^ORCID,He Ben¹,Khan Tuhina¹²^ORCID,Vatinel Rodolphe¹,Koutroumpa Nikoletta M.³,Afantitis Antreas³^ORCID,Lesire Laetitia¹²,Sierocki Pierre¹²,Deprez Benoit¹²^ORCID,Deprez-Poulain Rebecca¹²^ORCID

Affiliation:

1. U1177 - Drugs and Molecules for Living Systems, Univ. Lille, Inserm, Institut Pasteur de Lille, F-59000 Lille, France

2. European Genomic Institute for Diabetes, EGID, University of Lille, F-59000 Lille, France

3. Novamechanics Ltd., Nicosia 1516, Cyprus

Funder

Agence Nationale de la Recherche

H2020 Marie Sklodowska-Curie Actions

Conseil R?gional Hauts-de-France

Metropole Europ?enne de Lille

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.jmedchem.4c00840

Reference100 articles.

1. ERAAP customizes peptides for MHC class I molecules in the endoplasmic reticulum

2. The aminopeptidase ERAAP shapes the peptide repertoire displayed by major histocompatibility complex class I molecules

3. An IFN-γ–induced aminopeptidase in the ER, ERAP1, trims precursors to MHC class I–presented peptides

4. The ER aminopeptidase ERAP1 enhances or limits antigen presentation by trimming epitopes to 8–9 residues

5. Concerted peptide trimming by human ERAP1 and ERAP2 aminopeptidase complexes in the endoplasmic reticulum

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