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ERAP2

From Wikipedia, the free encyclopedia
ERAP2
Available structures
PDBHuman UniProt search: PDBe RCSB
Identifiers
AliasesERAP2, L-RAP, LRAP, endoplasmic reticulum aminopeptidase 2
External IDsOMIM: 609497; HomoloGene: 75183; GeneCards: ERAP2; OMA:ERAP2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

64167

n/a

Ensembl

ENSG00000164308

n/a

UniProt

Q6P179

n/a

RefSeq (mRNA)

NM_001130140
NM_022350
NM_001329229
NM_001329233

n/a

RefSeq (protein)

NP_001123612
NP_001316158
NP_001316162
NP_071745

n/a

Location (UCSC)Chr 5: 96.88 – 96.92 Mbn/a
PubMed search[2]n/a
Wikidata
View/Edit Human

Endoplasmic reticulum aminopeptidase 2 (ERAP2) is a protein that in humans is encoded by the ERAP2 gene. ERAP2 is part of the M1 aminopeptidase family. It is expressed along with ERAP1 in the endoplasmic reticulum (ER). In the ER, both enzymes help process and present antigens by trimming the ends of precursor peptides. This creates the optimal pieces for display by Major Histocompatibility Complex (MHC) class I molecules.

Biology / Functions

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Expression

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ERAP2 expression is regulated by interferon gamma signalling. While ERAP2 and homologous enzyme ERAP1 are both expressed in immune cells, the expression of the enzymes is independently regulated in other tissues without significant correlation of expression levels. However, coordinated expression patterns have also been observed, in which ERAP2 downregulation is counterbalanced by an increase in ERAP1 expression.[3] Overexpression of ERAP2 in various cancer types, including melanomas and different adenocarcinomas, has been suggested to modulate the presentation of cancer antigens on MHC-I, which may affect cancer invasion by immune cells.[4] ERAP2 is not expressed in mice making it more difficult to study.

Antigen presentation

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Unlike ERAP1, ERAP2 can trim efficiently peptides that already have optimal length for MHC class I presentation. Thus ERAP2 has been shown to shorten peptides of 9 or fewer amino acids, thereby destroying antigenic peptides in some cases.[5][6] ERAP2 displays a preference for peptide substrates that carry N-terminal basic residues (arginine, lysine).[7] A fraction of ERAP2 is reported to form complexes with ERAP1, as seen in co-precipitation experiments.[7] Heterodimer formation improves peptide-trimming efficiency, resulting in an expanded antigenic repertoire and a more diverse immune response.[8] The ERAP1-ERAP2 complex can trim free peptides in the ER and may also be able to trim MHC I-bound precursor peptides, according to some authors.[9] Individuals homozygous for ERAP2 haplotype B lack ERAP2 protein expression and have significantly lower MHC class I levels on the surface of B cells. This may result in an altered presentation of antigens and resulting immune responses.[10]

Other functions

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ERAP2 can modulate the renin-angiotensin system (RAS) in blood pressure homeostasis through angiotensin cleavage. In concert with ERAP1, ERAP2 counteracts angiotensin II activity, inducing vasodilation and hypertension reduction.[11] Blood pressure modulation by ERAP2 is supported by the association of ERAP2 with blood pressure progression and hypertension incidence.[12] Its link to pre-eclampsia in multiple populations shows further support for the role of ERAP2 in blood pressure homeostasis.[13][14]

Genetics / clinical significance

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Gene / location

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ERAP2 gene is located on human chromosome 5 in between the ERAP1 and LNPEP genes encoding the other two family members of the M1 aminopeptidases. It has 41,438 base pair length and consists of 19 exons.[15]

SNPs and disease association

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The ERAP2 gene is highly polymorphic and contains many common single nucleotide variants (SNVs) that are in strong linkage disequilibrium and are maintained at intermediate frequencies through balancing selection.[16] There are two common SNVs in ERAP2 that facilitate the alternative splicing of three haplotypes by altering splice motifs.[16][17] The A allele of splice variant rs2248374 tags haplotype A, which results in the full-length 960 amino acid long ERAP2 protein being produced.[16] However, the G allele of rs2248374 (i.e., haplotype B) disrupts splicing at exon 10, introducing downstream premature stop codons.[16] Under steady state conditions, the truncated mRNA is destroyed by nonsense mediated decay (NMD), but during influenza infections it is translated to two truncated isoforms.[18] Accordingly, 25% of the general population (haplotype B homozygotes) are deficient in full-length ERAP2 protein. The G allele of SNV rs17486481 activates a cryptic splice site upstream of exon 12 that also introduces premature stop codons and makes the transcript likely vulnerable to NMD (haplotype C). Different ERAP2 protein haplotypes (or allotypes) have been detected among the major continental populations based on common missense variants in ERAP2.[16][19] ERAP2 haplotypes are associated with severe inflammatory conditions (e.g., birdshot chorioretinopathy, Crohn's disease, ankylosing spondylitis, psoriasis) and cancer treatment responses.[20] Interestingly, the alleles from SNVs that strongly predispose to autoimmune conditions (i.e., A allele of rs2248374 and other SNVs in haplotype A) display natural selection in recent human history, which has been suggested to provide higher resistance against severe respiratory illnesses, including the bubonic plague ("Black Death"), pneumonia and COVID-19.[21][22][23] Klunk et al. found that individuals with the protective allele (dominant in the present European population) had a fivefold increase in ERAP2 expression in macrophages resulting in reduced replication of Y. pestis.

Structure / Mechanism

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Structure

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ERAP2 is composed of 4 structural units (I-IV), with the HEXXHX18E zinc-binding motif and the known GAMEN aminopeptidase motif located in domain II, similarly to its closely related enzyme ERAP1. The catalytic site features a single Zn(II) ion and is coordinated by two histidine residues (H370, H374) and a glutamate residue (E393). Domains II and IV, which are linked by domain III, form a large internal cavity close to the catalytic site and exclude the external solvent, in accordance with the “closed” conformation obtained for ERAP1.[24]

Mechanism

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ERAP2 selects substrates by sequestering them in its internal cavity and allowing interactions to determine trimming rates, thus combining substrate permissiveness with sequence bias.[25] A crystal structure of ERAP2 with a peptide product located in this cavity has revealed lack of deep specificity pockets and lack of a cavity that interacts with the peptide C- terminus, which justify the limited selectivity of this enzyme and the differences in length selection compared to ERAP1 (ERAP2 can effectively trim 8-mer peptides, while it is less active with longer substrates[25][26]). Interactions between side-chains of a 10-mer phosphinic analogue and residues of the interior of the cavity also appear shallow and opportunistic, further confirming its ability to process a variety of peptide substrates[27].  In terms of N-terminal residue specificity, ERAP2 prefers basic amino acids, such as arginine.[26]

Interactions

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Some experimental evidence has suggested the formation of a heterodimer between ERAP2 and the homologous enzyme ERAP1. Formation of leucine zipper-fused heterodimers of ERAP1 and ERAP2 produces mature epitopes more efficiently than a dilute mixture of the two enzymes. The interaction of ERAP2 with ERAP1 changes basic enzymatic parameters of the latter and improves its substrate-binding affinity.[28] A possible dimerization between ERAP1/ERAP2 could be the basis for enhanced synergism between these two enzymes which helps define the human immunopeptidome.[29]

Therapeutic approaches and pharmacology

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Therapeutic approaches for ERAP2 regulation rely mostly on the development of small molecule inhibitors. The most explored classes of inhibitors for ERAP2 are the allosteric site ones.

Figure 1. A. Crystal structure of ERAP2 co-crystallized with hydroxamic acid triazole in the active site. Adapted and recreated from PDB code 7NSK.[30] B. 2D chemical structure of co-crystallized compound.

ERAP2 catalytic site inhibitors

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  • Phosphinic derivatives

Although most of the phosphinic pseudopeptide analogs disclosed by Kokkala et al. in 2016 were non-selective ERAP inhibitors, compound 1 displayed nanomolar potency towards ERAP2 (IC50 = 129 nM) with a highly improved selectivity against ERAP1, and was active in modulating the immunopeptidome of cancer cells.[31][32]

  • Hydroxamic acid triazoles

In 2022, the first nanomolar selective ERAP2 inhibitors were discovered by kinetic-target guided synthesis (KTGS). A central core structure of hydroxamic acid triazoles targets the zinc ion in the catalytic site. Further investigations to optimize the activity led to nanomolar inhibitor BDM88952 (IC50 = 3.9 nM) with the relative protein-ligand interactions studied by ERAP2 X-ray co-crystallography (Figure 1).[30]

  • Carboxylic acids

Two hits of carboxylic acid derivatives were identified via high-throughput screening (HTS) against ERAP2, from an in-house library of 1920 compounds. Compound 3 was amongst those selected for their potency (ERAP2, IC50 = 22 nM) and selectivity. Docking studies revealed that the carboxylic acid is predicted to coordinate the catalytic zinc ion within ERAP2. Several analogues were designed and synthesized.[33]

ERAP2 allosteric site inhibitors

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  • Sulfonamides

Sulfonamide compound 4 was identified as a potential allosteric inhibitor against ERAP2 in 2022 by Arya et al..[34] This compound targets ERAP2 through an uncompetitive manner (IC50 = 44 μM) by inhibiting the hydrolysis of peptide substrates. At the same time it acts as a competitive inhibitor against ERAP1 (IC50 = 73 μM).[34]

Table 1. Representative examples of reported ERAP2 inhibitors. *IC50 value measured on long-peptide assay.

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000164308 – Ensembl, May 2017
  2. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. ^ Mattorre B, Tedeschi V, Paldino G, Fiorillo MT, Paladini F, Sorrentino R (2022). "The emerging multifunctional roles of ERAP1, ERAP2 and IRAP between antigen processing and renin-angiotensin system modulation". Frontiers in Immunology. 13: 1002375. doi:10.3389/fimmu.2022.1002375. PMC 9531115. PMID 36203608.
  4. ^ Lee ED (August 2017). "Endoplasmic Reticulum Aminopeptidase 2, a common immunological link to adverse pregnancy outcomes and cancer clearance?". Placenta. Exploring common mechanisms between placental and tumour growth. 56: 40–43. doi:10.1016/j.placenta.2017.03.012. PMC 5522626. PMID 28343731.
  5. ^ López de Castro JA (2018). "How ERAP1 and ERAP2 Shape the Peptidomes of Disease-Associated MHC-I Proteins". Frontiers in Immunology. 9: 2463. doi:10.3389/fimmu.2018.02463. PMC 6219399. PMID 30425713.
  6. ^ Martín-Esteban A, Rodriguez JC, Peske D, Lopez de Castro JA, Shastri N, Sadegh-Nasseri S (2022). "The ER Aminopeptidases, ERAP1 and ERAP2, synergize to self-modulate their respective activities". Frontiers in Immunology. 13: 1066483. doi:10.3389/fimmu.2022.1066483. PMC 9774488. PMID 36569828.
  7. ^ a b Saveanu L, Carroll O, Lindo V, Del Val M, Lopez D, Lepelletier Y, et al. (July 2005). "Concerted peptide trimming by human ERAP1 and ERAP2 aminopeptidase complexes in the endoplasmic reticulum". Nature Immunology. 6 (7): 689–697. doi:10.1038/ni1208. PMID 15908954.
  8. ^ Evnouchidou I, Weimershaus M, Saveanu L, van Endert P (July 2014). "ERAP1-ERAP2 dimerization increases peptide-trimming efficiency". Journal of Immunology. 193 (2): 901–908. doi:10.4049/jimmunol.1302855. PMID 24928998.
  9. ^ Chen H, Li L, Weimershaus M, Evnouchidou I, van Endert P, Bouvier M (August 2016). "ERAP1-ERAP2 dimers trim MHC I-bound precursor peptides; implications for understanding peptide editing". Scientific Reports. 6 (1): 28902. Bibcode:2016NatSR...628902C. doi:10.1038/srep28902. PMC 4981824. PMID 27514473.
  10. ^ Andrés AM, Dennis MY, Kretzschmar WW, Cannons JL, Lee-Lin SQ, Hurle B, et al. (October 2010). "Balancing selection maintains a form of ERAP2 that undergoes nonsense-mediated decay and affects antigen presentation". PLOS Genetics. 6 (10): e1001157. doi:10.1371/journal.pgen.1001157. PMC 2954825. PMID 20976248.
  11. ^ Tanioka T, Hattori A, Masuda S, Nomura Y, Nakayama H, Mizutani S, et al. (August 2003). "Human leukocyte-derived arginine aminopeptidase. The third member of the oxytocinase subfamily of aminopeptidases". The Journal of Biological Chemistry. 278 (34): 32275–32283. doi:10.1074/jbc.m305076200. PMID 12799365.
  12. ^ Zee RY, Rivera A, Inostroza Y, Ridker PM, Chasman DI, Romero JR (2018). "Gene Variation of Endoplasmic Reticulum Aminopeptidases 1 and 2, and Risk of Blood Pressure Progression and Incident Hypertension among 17,255 Initially Healthy Women". International Journal of Genomics. 2018: 2308585. doi:10.1155/2018/2308585. PMC 5933071. PMID 29850473.
  13. ^ Soltani S, Nasiri M (June 2019). "Association of ERAP2 gene variants with risk of pre-eclampsia among Iranian women". International Journal of Gynaecology and Obstetrics. 145 (3): 337–342. doi:10.1002/ijgo.12816. PMID 30933316.
  14. ^ Ferreira LC, Gomes CE, Duggal P, De Paula Holanda I, de Lima AS, do Nascimento PR, et al. (March 2021). "Genetic association of ERAP1 and ERAP2 with eclampsia and preeclampsia in northeastern Brazilian women". Scientific Reports. 11 (1): 6764. Bibcode:2021NatSR..11.6764F. doi:10.1038/s41598-021-86240-z. PMC 7990956. PMID 33762660.
  15. ^ "National Center for Biotechnology Information".
  16. ^ a b c d e Andrés AM, Dennis MY, Kretzschmar WW, Cannons JL, Lee-Lin SQ, Hurle B, et al. (October 2010). Gojobori T (ed.). "Balancing selection maintains a form of ERAP2 that undergoes nonsense-mediated decay and affects antigen presentation". PLOS Genetics. 6 (10): e1001157. doi:10.1371/journal.pgen.1001157. PMC 2954825. PMID 20976248.
  17. ^ Saunders H (1986). "A longitudinal study of the age-dependence of human ocular refraction—I. Age-dependent changes in the equivalent sphere". Ophthalmic and Physiological Optics. 6 (1): 39–46. doi:10.1016/0275-5408(86)90116-x. ISSN 0275-5408. PMID 3714274.
  18. ^ Ye CJ, Chen J, Villani AC, Gate RE, Subramaniam M, Bhangale T, et al. (December 2018). "Genetic analysis of isoform usage in the human anti-viral response reveals influenza-specific regulation of ERAP2 transcripts under balancing selection". Genome Research. 28 (12): 1812–1825. doi:10.1101/gr.240390.118. PMC 6280757. PMID 30446528.
  19. ^ Mattorre B, Tedeschi V, Paldino G, Fiorillo MT, Paladini F, Sorrentino R (2022). "The emerging multifunctional roles of ERAP1, ERAP2 and IRAP between antigen processing and renin-angiotensin system modulation". Frontiers in Immunology. 13: 1002375. doi:10.3389/fimmu.2022.1002375. PMC 9531115. PMID 36203608.
  20. ^ Lim YW, Chen-Harris H, Mayba O, Lianoglou S, Wuster A, Bhangale T, et al. (December 2018). "Germline genetic polymorphisms influence tumor gene expression and immune cell infiltration". Proceedings of the National Academy of Sciences of the United States of America. 115 (50): E11701–E11710. Bibcode:2018PNAS..11511701L. doi:10.1073/pnas.1804506115. PMC 6294879. PMID 30463956.
  21. ^ Klunk J, Vilgalys TP, Demeure CE, Cheng X, Shiratori M, Madej J, et al. (November 2022). "Evolution of immune genes is associated with the Black Death". Nature. 611 (7935): 312–319. Bibcode:2022Natur.611..312K. doi:10.1038/s41586-022-05349-x. PMC 9580435. PMID 36261521.
  22. ^ Venema WJ, Hiddingh S, van Loosdregt J, Bowes J, Balliu B, de Boer JH, et al. (January 2024). "A cis-regulatory element regulates ERAP2 expression through autoimmune disease risk SNPs". Cell Genomics. 4 (1): 100460. doi:10.1016/j.xgen.2023.100460. PMC 10794781. PMID 38190099.
  23. ^ Hamilton F, Mentzer AJ, Parks T, Baillie JK, Smith GD, Ghazal P, et al. (April 2023). "Variation in ERAP2 has opposing effects on severe respiratory infection and autoimmune disease". American Journal of Human Genetics. 110 (4): 691–702. doi:10.1016/j.ajhg.2023.02.008. PMC 10119032. PMID 36889308.
  24. ^ Birtley JR, Saridakis E, Stratikos E, Mavridis IM (January 2012). "The crystal structure of human endoplasmic reticulum aminopeptidase 2 reveals the atomic basis for distinct roles in antigen processing". Biochemistry. 51 (1): 286–295. doi:10.1021/bi201230p. PMID 22106953.
  25. ^ a b Mpakali A, Giastas P, Mathioudakis N, Mavridis IM, Saridakis E, Stratikos E (October 2015). "Structural Basis for Antigenic Peptide Recognition and Processing by Endoplasmic Reticulum (ER) Aminopeptidase 2". The Journal of Biological Chemistry. 290 (43): 26021–26032. doi:10.1074/jbc.M115.685909. PMC 4646255. PMID 26381406.
  26. ^ a b Saveanu L, Carroll O, Lindo V, Del Val M, Lopez D, Lepelletier Y, et al. (July 2005). "Concerted peptide trimming by human ERAP1 and ERAP2 aminopeptidase complexes in the endoplasmic reticulum". Nature Immunology. 6 (7): 689–697. doi:10.1038/ni1208. PMID 15908954.
  27. ^ de Castro JA, Stratikos E (May 2019). "Intracellular antigen processing by ERAP2: Molecular mechanism and roles in health and disease". Human Immunology. 80 (5): 310–317. doi:10.1016/j.humimm.2018.11.001. PMID 30414458.
  28. ^ Evnouchidou I, Weimershaus M, Saveanu L, van Endert P (July 2014). "ERAP1-ERAP2 dimerization increases peptide-trimming efficiency". Journal of Immunology. 193 (2): 901–908. doi:10.4049/jimmunol.1302855. PMID 24928998.
  29. ^ Papakyriakou A, Mpakali A, Stratikos E (2022). "Can ERAP1 and ERAP2 Form Functional Heterodimers? A Structural Dynamics Investigation". Frontiers in Immunology. 13: 863529. doi:10.3389/fimmu.2022.863529. PMC 9065437. PMID 35514997.
  30. ^ a b Camberlein V, Fléau C, Sierocki P, Li L, Gealageas R, Bosc D, et al. (September 2022). "Discovery of the First Selective Nanomolar Inhibitors of ERAP2 by Kinetic Target-Guided Synthesis". Angewandte Chemie. 61 (39): e202203560. doi:10.1002/anie.202203560. PMC 9558494. PMID 35904863.
  31. ^ Kokkala P, Mpakali A, Mauvais FX, Papakyriakou A, Daskalaki I, Petropoulou I, et al. (October 2016). "Optimization and Structure-Activity Relationships of Phosphinic Pseudotripeptide Inhibitors of Aminopeptidases That Generate Antigenic Peptides". Journal of Medicinal Chemistry. 59 (19): 9107–9123. doi:10.1021/acs.jmedchem.6b01031. PMID 27606717.
  32. ^ Temponeras I, Stamatakis G, Samiotaki M, Georgiadis D, Pratsinis H, Panayotou G, et al. (February 2022). "ERAP2 Inhibition Induces Cell-Surface Presentation by MOLT-4 Leukemia Cancer Cells of Many Novel and Potentially Antigenic Peptides". International Journal of Molecular Sciences. 23 (3): 1913. doi:10.3390/ijms23031913. PMC 8836666. PMID 35163832.
  33. ^ Laura M, Ronan G, Vy LB, Valentin G, Omar CA, Virgyl C, et al. (February 2021). "Modulators of hERAP2 discovered by high-throughput screening". European Journal of Medicinal Chemistry. 211: 113053. doi:10.1016/j.ejmech.2020.113053. PMID 33359953.
  34. ^ a b Arya R, Maben Z, Rane D, Ali A, Stern LJ (July 2022). "Phenylsulfamoyl Benzoic Acid Inhibitor of ERAP2 with a Novel Mode of Inhibition". ACS Chemical Biology. 17 (7): 1756–1768. doi:10.1021/acschembio.2c00093. PMID 35767698.
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