Polymorphism in F pocket affects peptide selection and stability of type 1 diabetes‐associated HLA‐B39 allotypes

• Published in: European journal of immunology 2024-06, Vol.54 (6), p.e2350683-n/a
• Main Authors: Amarajeewa, A. W. Peshala, Özcan, Aslihan, Mukhtiar, Alveena, Ren, Xu, Wang, Qianyu, Ozbek, Pemra, Garstka, Malgorzata A., Serçinoğlu, Onur
• Format: Article
• Language: English
• Subjects: Allotypes; Cell surface; Diabetes; Diabetes mellitus (insulin dependent); Histocompatibility antigen HLA; HLA‐B39; Local frustration; Molecular dynamics; Molecular modelling; Pathogenesis; Peptide selection; Peptides; Type 1 diabetes
• ISSN: 0014-2980; 1521-4141; 1521-4141
• DOI: 10.1002/eji.202350683

HLA‐B*39:06, HLA‐B*39:01, and HLA‐B*38:01 are closely related HLA allotypes differentially associated with type 1 diabetes (T1D) risk and progression. B*39:06 is highly predisposing, while B*39:01 and B*38:01 are weakly predisposing and protective allotypes, respectively. Here, we aimed to decipher molecular mechanisms underlying the differential association of these allotypes with T1D pathogenesis. We addressed peptide binding and conformational stability of HLA‐B allotypes using computational and experimental approaches. Computationally, we found that B*39:06 and B*39:01 allotypes had more rigid peptide‐binding grooves and were more promiscuous in binding peptides than B*38:01. Peptidomes of B*39:06 and B*39:01 contained fewer strong binders and were of lower affinity than that of B*38:01. Experimentally, we demonstrated that B*39:06 and B*39:01 had a higher capacity to bind peptides and exit to the cell surface but lower surface levels and were degraded faster than B*38:01. In summary, we propose that promiscuous B*39:06 and B*39:01 may bind suboptimal peptides and transport them the cell surface, where such unstable complexes may contribute to the pathogenesis of T1D. B*39, T1D‐predisposing allotype has a rigid peptide‐binding groove and capacity to bind optimal (black) and suboptimal (red) peptides. B*38:0 T1D‐protective allotype has a flexible peptide‐binding groove and requires optimal peptides (black). As a result, more T1D‐predisposing allotypes pass medial‐Golgi and have the potential to signal to the immune system.