Structural basis for the stability of the swine major histocompatibility complex class I with heterologous β₂-microglobulin.

Authors

Dongmei Hu, Dongdong Yin, Jieru Wang, Yayun Liu, Nianzhi Zhang, Xiaocheng Pan

Published in

International journal of biological macromolecules. Pages 153186. Jun 23, 2026. Epub Jun 23, 2026.

Abstract

Establishing mouse models expressing heterologous major histocompatibility complex class I (MHC-I) molecules is an effective strategy for immunological research. However, murine β₂-microglobulin (mβ₂m) may interfere with the proper folding and peptide loading of the heterologous heavy chain. We found that mβ₂m can associate with SLA-1*1502 and the Porcine reproductive and respiratory syndrome virus (PRRSV)-derived epitope peptide (PPs) to form a complex, albeit with lower efficiency compared with swine β₂m (sβ₂m). We determined the crystal structure of the chimeric complex SLA-1*1502/mβ₂m/PP7. Comparison with the previously reported SLA-1*1502/sβ₂m/PP7 structure revealed that, although the overall conformations are similar, the interaction pattern between the heavy and light chains differs, exhibiting features characteristic of both murine and porcine origins. Interestingly, the peptide binding mode in the chimeric complex also exhibited distinct local features: the buried surface area between PP7 and the binding groove increased, and a new salt bridge was formed between PP7 and residue R114 of SLA-1*1502. Structural comparison of diverse cross-species chimeric complexes reveals that conformational shifts of bound epitope peptides are governed by the stability of the core hydrogen-bond network at the heavy-light chain interface, and substitution with human β₂m triggers milder local structural distortions than murine β₂m. In summary, our findings demonstrate that the differences between mβ₂m and sβ₂m influence both complex formation and peptide binding mode. Therefore, constructing mouse models co-expressing SLA-I and sβ₂m would be a more optimized strategy for related immunological studies.

PMID:
42336018
Bibliographic data and abstract were imported from PubMed on 24 Jun 2026.

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