MHC binding affects the dynamics of different T-cell receptors in different ways

MHC binding affects the dynamics of different T-cell receptors in different ways

Bibliográfalaš dieđut
Váldodahkkit:	Knapp, B, Van Der Merwe, P, Dushek, O, Deane, C
Materiálatiipa:	Journal article
Giella:	English
Almmustuhtton:	Public Library of Science 2019

Geahča maid

MHC binding affects the dynamics of different T-cell receptors in different ways.
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T cell receptor and coreceptor CD8 alphaalpha bind peptide-MHC independently and with distinct kinetics.
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Mechanisms for T cell receptor triggering.
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TCR–pMHC kinetics under force in a cell-free system show no intrinsic catch bond, but a minimal encounter duration before binding
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Fluctuations in T cell receptor and pMHC interactions regulate T cell activation
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Kinetics and mechanics of two-dimensional interactions between T cell receptors and different activating ligands.
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Basic residues in the T-cell receptor ζ cytoplasmic domain mediate membrane association and modulate signaling.
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Computationally profiling peptide:MHC recognition by T-cell receptors and T-cell receptor-mimetic antibodies
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Systems model of T cell receptor proximal signaling reveals emergent ultrasensitivity
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Systems model of T cell receptor proximal signaling reveals emergent ultrasensitivity
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CD8 helps TCR catch slippery self pMHC
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Variable regions of antibodies and T-cell receptors may not be sufficient in molecular simulations investigating binding.
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Structural features underlying T-cell receptor sensitivity to concealed MHC class I micropolymorphisms.
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Regulation of temporal cytokine production by co-stimulation receptors in TCR-T cells is lost in CAR-T cells
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Intrinsic disorder in the T cell receptor creates cooperativity and controls ZAP70 binding
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Effects of common mutations in the SARS-CoV-2 Spike RBD and its ligand, the human ACE2 receptor on binding affinity and kinetics
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Cooperative binding of T cell receptor and CD4 to peptide-MHC enhances antigen sensitivity
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pyHVis3D: Visualising Molecular Simulation deduced H-bond networks in 3D: Application to T-cell receptor interactions
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Human inhibitory receptors Ig-like transcript 2 (ILT2) and ILT4 compete with CD8 for MHC class I binding and bind preferentially to HLA-G.
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Decoupling peptide binding from T cell receptor recognition with engineered chimeric MHC-I molecules
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Quantifying conformational changes in the TCR:pMHC-I binding interface
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Elementary steps in T cell receptor triggering.
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Homodimerisation of the lymph vessel endothelial receptor LYVE-1 through a redox-labile disulfide is critical for hyaluronan binding in lymphatic endothelium
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Homodimerisation of the lymph vessel endothelial receptor LYVE-1 through a redox-labile disulfide is critical for hyaluronan binding in lymphatic endothelium
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T-cell receptors binding orientation over peptide/MHC class I is driven by long-range interactions.
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