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Small molecule probes of ERAP-1

Small molecule probes of ERAP-1
ERAP-1小分子探针
批准号:
8327981
负责人:
Lawrence J. Stern
金额:
$4.11万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-03-20 至 2014-02-28

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DESCRIPTION (provided by applicant): This project is directed at discovery of small-molecule chemical probes for ERAP1, an aminopeptidase involved in antigen presentation in the immune system. ERAP1 polymorphisms recently have been linked to autoimmune diseases including ankylosing spondylitis and psoriasis. ERAP1 is known to provide the final trimming steps for certain peptides before they are loaded onto class I MHC proteins, but the identity of these peptides and their role in development of autoimmune disease is not known. The broad long-term objective of this work is to understand ERAP1's role in immune system health and disease, and to develop therapeutic approaches to alleviation of autoimmune pathology. The specific aims of the research are to collaborate with the NIH Molecular Libraries Probe Center Network (MPLCN) to implement a validated high-throughput screen to identify small molecule inhibitors of ERAP1 (aim 1), to employ previously validated secondary assays to validate the biological relevance of identified hits (aim 2), and to colaborate with MLPCN to develop and characterize chemical probe(s) using a previously validated tertiary assay (aim 3).
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ER-aminopeptidases: Conformational regulation and antigen presentation function
ER-aminopeptidases: Conformational regulation and antigen presentation function
ER-aminopeptidases: Conformational regulation and antigen presentation function
HLA-DO / H2-O: modulation of MHC-II peptide diversity and Treg population control
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