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Updated: Dec 20, 2025

Evaluation of T Follicular Helper Cells and Germinal Center Response During Influenza A Virus Infection in Mice
Published on: June 27, 2020
Imitating the humoral immune response
1Lehrstuhl für Biologische Chemie, Technische Universität Munich, Wissenschaftszentrum Weihenstephan, An der Saatzucht 5, D-85350 Freising, Germany. skerra@wzw.tum.de
The immune system uses antibodies and genetic mechanisms for diverse binding. Researchers are adapting these principles to create novel artificial binding proteins for various applications.
Area of Science:
- Immunology
- Biotechnology
- Molecular Biology
Background:
- The immune system employs antibodies with immunoglobulin domains and hypervariable loops for molecular recognition.
- Genetic mechanisms, including gene segment recombination and hypermutation, generate antibody diversity at the somatic level.
Purpose of the Study:
- To explore the molecular mechanisms underlying immune system's binding capabilities.
- To adapt these principles for creating artificial binding proteins using combinatorial biotechnology.
Main Methods:
- Investigating the structural and genetic basis of antibody diversity.
- Applying combinatorial biotechnology techniques to engineer novel binding proteins.
- Utilizing alternative scaffolds like alpha-helical bundles and beta-barrels.
Main Results:
- Understanding of antibody structure-function relationships and diversity generation.
- Successful construction of novel receptor molecules from alternative scaffolds.
- Demonstration of artificial binding proteins' potential.
Conclusions:
- The principles of antibody diversity can be harnessed to create artificial binding proteins.
- Engineered binding proteins offer versatile tools for biomolecular recognition, targeting, and separation.
- These novel proteins have potential applications in research, technology, and medicine.
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Published on: September 7, 2018
04:47A Method to Assess Fc-mediated Effector Functions Induced by Influenza Hemagglutinin Specific Antibodies
Published on: February 23, 2018
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