Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Diversity of Antigen Receptors01:28

Diversity of Antigen Receptors

1.3K
Antigen receptors are essential components of the immune system crucial in defending the body against foreign invaders. These receptors are present on the surface of B and T cells, enabling them to recognize antigens and mount an appropriate immune response.
Before encountering any antigen, lymphocytes express these receptors. On B cells, the antigen receptor is a membrane-bound antibody molecule called BCR; on T cells, it is a T cell receptor or TCR. B and T cell receptors are composed of two...
1.3K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

COVID-19 Vaccine Reactogenicity Marks an Innate Inflammatory Response Associated With HLA Variation and Enhanced Protection.

Research square·2026
Same author

γδ T cell-derived IL-4 initiates CD8<sup>+</sup> T cell immunity.

Nature immunology·2026
Same author

Preclinical development of a cross-protective β-SARS-CoV-2 virus-like particle vaccine adjuvanted with MF59.

NPJ vaccines·2026
Same author

An HLA Association With COVID-19 Vaccine Reactogenicity Correlates With Fewer SARS-CoV-2 Infections and Monocyte Activation.

Research square·2026
Same author

Adaptive Immunity and Alzheimer's Disease: Dual Roles in Neurodegeneration and Neuroprotection with Therapeutic Implications.

Biomolecules & therapeutics·2026
Same author

Method for Performing T Cell Receptor-Peptide-Human Leukocyte Antigen Co-complexation and Structural Analysis.

Methods in molecular biology (Clifton, N.J.)·2026

Related Experiment Video

Updated: Jan 7, 2026

Generating De Novo Antigen-specific Human T Cell Receptors by Retroviral Transduction of Centric Hemichain
08:48

Generating De Novo Antigen-specific Human T Cell Receptors by Retroviral Transduction of Centric Hemichain

Published on: October 25, 2016

9.0K

Method for Producing Recombinant Soluble T-Cell Receptors.

You Min Ahn1,2, Stephanie Gras1,2,3, Demetra S M Chatzileontiadou4,5,6

  • 1Infection and Immunity Program, La Trobe Institute for Molecular Science (LIMS), La Trobe University, Bundoora, VIC, Australia.

Methods in Molecular Biology (Clifton, N.J.)
|January 1, 2026
PubMed
Summary

This chapter details producing soluble T cell receptors (TCRs), crucial for understanding how T cells recognize peptide-Human Leukocyte Antigen (pHLA) complexes. This knowledge aids in studying immune responses and host defense mechanisms.

Keywords:
Bacterial expressionChromatographyInclusion BodyPurificationT cell receptor

More Related Videos

Streamlined Single Cell TCR Isolation and Generation of Retroviral Vectors for In Vitro and In Vivo Expression of Human TCRs
11:21

Streamlined Single Cell TCR Isolation and Generation of Retroviral Vectors for In Vitro and In Vivo Expression of Human TCRs

Published on: September 10, 2017

10.0K
Using X-ray Crystallography, Biophysics, and Functional Assays to Determine the Mechanisms Governing T-cell Receptor Recognition of Cancer Antigens
09:53

Using X-ray Crystallography, Biophysics, and Functional Assays to Determine the Mechanisms Governing T-cell Receptor Recognition of Cancer Antigens

Published on: February 6, 2017

11.8K

Related Experiment Videos

Last Updated: Jan 7, 2026

Generating De Novo Antigen-specific Human T Cell Receptors by Retroviral Transduction of Centric Hemichain
08:48

Generating De Novo Antigen-specific Human T Cell Receptors by Retroviral Transduction of Centric Hemichain

Published on: October 25, 2016

9.0K
Streamlined Single Cell TCR Isolation and Generation of Retroviral Vectors for In Vitro and In Vivo Expression of Human TCRs
11:21

Streamlined Single Cell TCR Isolation and Generation of Retroviral Vectors for In Vitro and In Vivo Expression of Human TCRs

Published on: September 10, 2017

10.0K
Using X-ray Crystallography, Biophysics, and Functional Assays to Determine the Mechanisms Governing T-cell Receptor Recognition of Cancer Antigens
09:53

Using X-ray Crystallography, Biophysics, and Functional Assays to Determine the Mechanisms Governing T-cell Receptor Recognition of Cancer Antigens

Published on: February 6, 2017

11.8K

Area of Science:

  • Immunology
  • Structural Biology
  • Biochemistry

Background:

  • T cells are vital for adaptive immunity, identifying and eliminating pathogens.
  • T cell recognition relies on T cell receptors (TCRs) binding to peptide-Human Leukocyte Antigen (pHLA) complexes.
  • Understanding TCR-pHLA interactions is key to T cell activation and host defense.

Purpose of the Study:

  • To describe the methodology for producing soluble T cell receptors (TCRs).
  • To facilitate structural and functional studies of TCR-pHLA interactions.
  • To advance the understanding of T cell-mediated immune responses.

Main Methods:

  • Production of soluble T cell receptors (TCRs).
  • Utilizing X-ray crystallography to determine the structure of TCR-pHLA complexes.
  • Purification and characterization of soluble TCR and pHLA proteins.

Main Results:

  • Established a method for generating soluble TCRs suitable for structural analysis.
  • Provided insights into the molecular interactions between TCRs and pHLA complexes.
  • The structural data illuminates the mechanism of T cell recognition.

Conclusions:

  • Soluble TCR production is feasible and essential for structural studies.
  • Detailed structural information on TCR-pHLA complexes enhances understanding of T cell activation.
  • This work supports further research into T cell immunology and therapeutic development.