6MHR
Structure of the human 4-1BB / Urelumab Fab complex
Summary for 6MHR
Entry DOI | 10.2210/pdb6mhr/pdb |
Related | 6MGE 6MGP |
Descriptor | Urelumab Fab heavy chain, Urelumab Fab kappa chain, Tumor necrosis factor receptor superfamily member 9, ... (9 entities in total) |
Functional Keywords | signaling, tnfrsf, 4-1bb, cd137, immune system, therapeutic antibody, complex |
Biological source | Homo sapiens (human) More |
Total number of polymer chains | 6 |
Total formula weight | 131534.30 |
Authors | Kimberlin, C.R.,Chin, S.M.,Roe-Zurz, Z.,Xu, A.,Yang, Y. (deposition date: 2018-09-18, release date: 2018-11-21, Last modification date: 2024-10-16) |
Primary citation | Chin, S.M.,Kimberlin, C.R.,Roe-Zurz, Z.,Zhang, P.,Xu, A.,Liao-Chan, S.,Sen, D.,Nager, A.R.,Oakdale, N.S.,Brown, C.,Wang, F.,Yang, Y.,Lindquist, K.,Yeung, Y.A.,Salek-Ardakani, S.,Chaparro-Riggers, J. Structure of the 4-1BB/4-1BBL complex and distinct binding and functional properties of utomilumab and urelumab. Nat Commun, 9:4679-4679, 2018 Cited by PubMed Abstract: 4-1BB (CD137, TNFRSF9) is an inducible costimulatory receptor expressed on activated T cells. Clinical trials of two agonist antibodies, utomilumab (PF-05082566) and urelumab (BMS-663513), are ongoing in multiple cancer indications, and both antibodies demonstrate distinct activities in the clinic. To understand these differences, we solved structures of the human 4-1BB/4-1BBL complex, the 4-1BBL trimer alone, and 4-1BB bound to utomilumab or urelumab. The 4-1BB/4-1BBL complex displays a unique interaction between receptor and ligand when compared with other TNF family members. Furthermore, our ligand-only structure differs from previously published data. Utomilumab, a ligand-blocking antibody, binds 4-1BB between CRDs 3 and 4. In contrast, urelumab binds 4-1BB CRD-1, away from the ligand binding site. Finally, cell-based assays demonstrate utomilumab is a milder agonist than urelumab. Collectively, our data provide a deeper understanding of the 4-1BB signaling complex, providing a template for future development of next generation 4-1BB targeted biologics. PubMed: 30410017DOI: 10.1038/s41467-018-07136-7 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.8 Å) |
Structure validation
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