TCR

TCR quantifies geometries of T cell receptor (TCR) binding modes with peptide/MHC (pMHC) complexes to analyze how variations in binding geometry influence T cell signaling and structural recognition.


Key Features:

  • Comprehensive Geometrical Quantification: Quantifies complex TCR–pMHC geometries beyond simple descriptors such as crossing angles to capture detailed binding-mode parameters.
  • Class-Specific Binding Analysis: Distinguishes between class I and class II peptide/MHC complexes to reveal class-dependent differences in TCR access to peptide antigens.
  • Enhanced Biological Insights: Relates geometric parameters of TCR binding modes to variations in T cell signaling, binding affinity outliers, and functional outcomes.
  • Data-Driven Modeling: Supports modeling of structural properties of TCR–peptide/MHC complexes from sequence information.

Scientific Applications:

  • Exploring TCR–pMHC Interactions: Enables detailed analysis of geometric parameters that govern TCR recognition of peptide/MHC complexes.
  • Understanding T Cell Signaling Variability: Facilitates investigation of how differences in binding geometry contribute to variable T cell signaling and function.
  • Structural Biology Research: Supports structural characterization and comparative analysis of TCR binding modes within immunological studies.

Methodology:

Computational quantification of TCR–pMHC geometries and modeling of structural properties from sequence information.

Topics

Details

License:
LGPL-3.0
Programming Languages:
Python
Added:
1/9/2020
Last Updated:
11/24/2024

Operations

Publications

Singh NK, Abualrous ET, Ayres CM, Noé F, Gowthaman R, Pierce BG, Baker BM. Geometrical characterization of T cell receptor binding modes reveals class‐specific binding to maximize access to antigen. Proteins: Structure, Function, and Bioinformatics. 2019;88(3):503-513. doi:10.1002/prot.25829. PMID:31589793. PMCID:PMC6982585.

PMID: 31589793
PMCID: PMC6982585
Funding: - National Institute of General Medical Sciences: R01GM126299, R35GM118166 - Deutsche Forschungsgemeinschaft: SFB 958/A7, SFB740/D7, SFB958/A4

Links