# Structural Basis of MERS‐CoV Receptor Interactions and Antibody Neutralisations

**Authors:** Edem Gavor, Yeu Khai Choong, Sunil Singh, Hariharan Sivaraman, Er Shi Yin, J. Sivaraman

PMC · DOI: 10.1002/rmv.70113 · Reviews in Medical Virology · 2026-02-27

## TL;DR

This paper reviews MERS-CoV's receptor interactions and antibody responses to guide the development of antivirals and vaccines.

## Contribution

The paper provides structural insights into MERS-CoV spike glycoprotein-antibody complexes to inform next-generation pan-coronavirus vaccines.

## Key findings

- MERS-CoV has a high mortality rate and remains a significant public health threat.
- Structural analysis of spike glycoprotein-antibody complexes reveals mechanisms of antibody neutralization.
- Current efforts focus on developing cross-reactive antibodies and vaccines for MERS-CoV and other coronaviruses.

## Abstract

Increasing outbreaks of coronaviruses underscore the importance of antivirals and vaccines that can combat a wide range of coronaviruses. Neutralising antibodies (nAbs), along with vaccines and small‐molecule drugs, are among the most promising treatments and prevention options against coronaviruses. Here, we focus on Middle East Respiratory Syndrome coronavirus (MERS‐CoV) and discuss receptor usage and current progress in antibody research against MERS‐CoV infections. First detected in Saudi Arabia and Jordan in 2012, MERS‐CoV is a lethal zoonotic pathogen. MERS‐CoV infections have been reported by 27 countries between April 2012 till now, with 953 deaths (∼35% mortality) (5 new infections and 4 fatalities reported as of 1 October 2024). WHO identified MERS‐CoV as a high‐threat pathogen due to its severity, high mortality rate, and potential for epidemic or pandemic spread with recent outbreaks and deaths raising more concerns amidst the COVID‐19 pandemic. As of now, there is no antiviral drugs or vaccine against MERS‐CoV available. Here we provide a perspective on receptor usage, the risk of MERS‐CoV and other CoVs evolution on future pandemics, and the mechanisms of MERS‐CoV‐derived nAbs. We offer insight into how these antibodies cross‐react and cross‐neutralise by analysing available structures of spike glycoprotein–antibody complexes. This review provides an update and a basis for the development of antibodies and vaccines for MERS‐CoV, and possibly for the designing of next‐generation pan‐coronavirus vaccines and antivirals.

## Linked entities

- **Proteins:** S (surface glycoprotein)

## Full-text entities

- **Genes:** ERVK-6 (endogenous retrovirus group K member 6, envelope) [NCBI Gene 64006] {aka ERVK6, HERV-K(C7), HERV-K108, K-Rev, c-orf, cORF}, VTN (vitronectin) [NCBI Gene 7448] {aka V75, VN, VNT}, NRP1 (neuropilin 1) [NCBI Gene 8829] {aka BDCA4, CD304, NP1, NRP, VEGF165R}, IFNAR1 (interferon alpha and beta receptor subunit 1) [NCBI Gene 3454] {aka AVP, CRF2-1, IFN-R-1, IFN-alpha-REC, IFNAR, IFNBR}, Membrane Protein [NCBI Gene 14254600], KREMEN1 (kringle containing transmembrane protein 1) [NCBI Gene 83999] {aka ECTD13, KREMEN, KRM1}, CDK1 (cyclin dependent kinase 1) [NCBI Gene 983] {aka CDC2, CDC28A, P34CDC2}, FANCB (FA complementation group B) [NCBI Gene 2187] {aka FA2, FAAP90, FAAP95, FAB, FACB}, ACE2 (angiotensin converting enzyme 2) [NCBI Gene 59272] {aka ACEH}, RBMY2DP (RNA binding motif protein Y-linked family 2 member D, pseudogene) [NCBI Gene 347598] {aka RBM, RBMY2}, LRRC15 (leucine rich repeat containing 15) [NCBI Gene 131578] {aka LIB}, DPP4 (dipeptidyl peptidase 4) [NCBI Gene 1803] {aka ADABP, ADCP2, CD26, DPPIV, TP103}, MLC1 (modulator of VRAC current 1) [NCBI Gene 23209] {aka LVM, MLC, VL}, BSG (basigin (Ok blood group)) [NCBI Gene 682] {aka 5F7, CD147, EMMPRIN, EMPRIN, HAb18G, OK}, AXL (AXL receptor tyrosine kinase) [NCBI Gene 558] {aka ARK, AXL3, JTK11, Tyro7, UFO}, ASGR1 (asialoglycoprotein receptor 1) [NCBI Gene 432] {aka ASGPR, ASGPR1, CLEC4H1, HL-1}, TMEM106B (transmembrane protein 106B) [NCBI Gene 54664] {aka HLD16}, Spike Glycoprotein [NCBI Gene 14254594]
- **Diseases:** shortness of breath (MESH:D004417), gastrointestinal symptoms (MESH:D012817), fever (MESH:D005334), pneumonia (MESH:D011014), diarrhoea (MESH:D003967), infected (MESH:D007239), fatalities (MESH:C565541), COVID-19 (MESH:D000086382), coughing (MESH:D003371), deaths (MESH:D003643), MERS infections (MESH:D018352), SARS (MESH:D045169), type 2 diabetes mellitus (MESH:D003924)
- **Chemicals:** glycan (MESH:D011134), sialic acid (MESH:D019158), 5F9 (MESH:C000626278), Amino Acids (MESH:D000596), 1.10f3 (-), glucose (MESH:D005947), C2 (MESH:C023714)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Human coronavirus OC43 (no rank) [taxon 31631], Human coronavirus HKU1 (no rank) [taxon 290028], hepatitis C virus [taxon 11103], Middle East respiratory syndrome-related coronavirus (no rank) [taxon 1335626], Human coronavirus 229E (no rank) [taxon 11137], Human immunodeficiency virus 1 (no rank) [taxon 11676], Severe acute respiratory syndrome-related coronavirus (no rank) [taxon 694009], Gammacoronavirus (genus) [taxon 694013], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606], Orthomyxoviridae (family) [taxon 11308], Respiratory syncytial virus (no rank) [taxon 12814], Human immunodeficiency virus (species) [taxon 12721], Influenza A virus (no rank) [taxon 11320], Coronaviridae (family) [taxon 11118], Bacillus sp. AT (species) [taxon 1196779], Human coronavirus NL63 (no rank) [taxon 277944], Betacoronavirus (genus) [taxon 694002]
- **Mutations:** Asp539Arg, Asp509Gly, Arg511, E536 R, Leu506, Asp539, Asp539Asn, Asp510Gly, Leu452Arg, Gly198Asp, Glu536, Val534, I529 T, Asp509, Gly484Lys, L506 F, Ser28Pro, Ile529, Glu484Lys, Thr478Lys, Val534Ala, 510Thr to Phe, Asp510, Thr to Phe, Phe506Leu, Gly-Asp, E484D, Arg511Ala, Glu484 to Asp
- **Cell lines:** S2 — Drosophila melanogaster (Fruit fly), Spontaneously immortalized cell line (CVCL_Z232), NCI-H1975 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_1511), HDPP4 — Homo sapiens (Human), Ataxia telangiectasia syndrome, Finite cell line (CVCL_F083)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12949372/full.md

## References

97 references — full list in the complete paper: https://tomesphere.com/paper/PMC12949372/full.md

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Source: https://tomesphere.com/paper/PMC12949372