The genetics, structure and function of the M1 aminopeptidase oxytocinase subfamily and their therapeutic potential in immune-mediated disease

被引:19
|
作者
Hanson, Aimee L. [1 ,2 ]
Morton, Craig J. [3 ,4 ]
Parker, Michael W. [3 ,4 ]
Bessette, Darrell [2 ,5 ]
Kenna, Tony J. [2 ,5 ]
机构
[1] Univ Queensland, Diamantina Inst, Brisbane, Qld, Australia
[2] Princess Alexandra Hosp, Translat Res Inst, Brisbane, Qld, Australia
[3] Univ Melbourne, Dept Biochem & Mol Biol, Mol Sci & Biotechnol Inst Bio21, Parkville, Vic, Australia
[4] St Vincents Inst Med Res, Australian Canc Res Fdn, Rat Drug Discovery Ctr, Fitzroy, Vic, Australia
[5] Queensland Univ Technol, Fac Hlth, Inst Hlth & Biomed Innovat, Brisbane, Qld, Australia
关键词
Aminopeptidase; Antigen presentation; Autoimmunity; Inhibitor; INSULIN-REGULATED AMINOPEPTIDASE; ENDOPLASMIC-RETICULUM AMINOPEPTIDASES; GENOME-WIDE ASSOCIATION; PSORIASIS SUSCEPTIBILITY LOCI; UNFOLDED PROTEIN RESPONSE; ANKYLOSING-SPONDYLITIS; LEUCINE AMINOPEPTIDASE; SELECTIVE INHIBITORS; BEHCETS-DISEASE; CRYSTAL-STRUCTURES;
D O I
10.1016/j.humimm.2018.11.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The oxytocinase subfamily of M1 aminopeptidases plays an important role in processing and trimming of peptides for presentation on major histocompatibility (MHC) Class I molecules. Several large-scale genomic studies have identified association of members of this family of enzymes, most notably ERAP1 and ERAP2, with immune-mediated diseases including ankylosing spondylitis, psoriasis and birdshot chorioretinopathy. Much is now known about the genetics of these enzymes and how genetic variants alter their function, but how these variants contribute to disease remains largely unresolved. Here we discuss what is known about their structure and function and highlight some of the knowledge gaps that affect development of drugs targeting these enzymes.
引用
收藏
页码:281 / 289
页数:9
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