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6J0L

Crystal structure of intracellular B30.2 domain of BTN3A3 mutant in complex with sulfate ion

Summary for 6J0L
Entry DOI10.2210/pdb6j0l/pdb
DescriptorButyrophilin subfamily 3 member A3, SULFATE ION (3 entities in total)
Functional Keywordsbutyrophilin, signaling protein
Biological sourceHomo sapiens (Human)
Total number of polymer chains2
Total formula weight51313.34
Authors
Yang, Y.Y.,Liu, W.D.,Cai, N.N.,Chen, C.C.,Guo, R.T.,Zhang, Y.H. (deposition date: 2018-12-24, release date: 2019-04-03, Last modification date: 2023-11-22)
Primary citationYang, Y.,Li, L.,Yuan, L.,Zhou, X.,Duan, J.,Xiao, H.,Cai, N.,Han, S.,Ma, X.,Liu, W.,Chen, C.C.,Wang, L.,Li, X.,Chen, J.,Kang, N.,Chen, J.,Shen, Z.,Malwal, S.R.,Liu, W.,Shi, Y.,Oldfield, E.,Guo, R.T.,Zhang, Y.
A Structural Change in Butyrophilin upon Phosphoantigen Binding Underlies Phosphoantigen-Mediated V gamma 9V delta 2 T Cell Activation.
Immunity, 50:1043-, 2019
Cited by
PubMed Abstract: Human Vγ9Vδ2 T cells respond to microbial infections and malignancy by sensing diphosphate-containing metabolites called phosphoantigens, which bind to the intracellular domain of butyrophilin 3A1, triggering extracellular interactions with the Vγ9Vδ2 T cell receptor (TCR). Here, we examined the molecular basis of this "inside-out" triggering mechanism. Crystal structures of intracellular butyrophilin 3A proteins alone or in complex with the potent microbial phosphoantigen HMBPP or a synthetic analog revealed key features of phosphoantigens and butyrophilins required for γδ T cell activation. Analyses with chemical probes and molecular dynamic simulations demonstrated that dimerized intracellular proteins cooperate in sensing HMBPP to enhance the efficiency of γδ T cell activation. HMBPP binding to butyrophilin doubled the binding force between a γδ T cell and a target cell during "outside" signaling, as measured by single-cell force microscopy. Our findings provide insight into the "inside-out" triggering of Vγ9Vδ2 T cell activation by phosphoantigen-bound butyrophilin, facilitating immunotherapeutic drug design.
PubMed: 30902636
DOI: 10.1016/j.immuni.2019.02.016
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.95 Å)
Structure validation

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