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University of Illinois at Urbana-Champaign

Directed Evolution of T Cell Receptor Antagonists

Abstract

dc:description

In Chapter 4, further engineering of TCR stability mutants to produce increased affinity binding for SAg is described. An optimized TCR fragment (containing nine mutations) was isolated after mutagenesis and selection, and was found to have approximately 1000-fold improved affinity for SAg. A soluble form of the mutant was shown to completely and specifically inhibit T cell activity in vitro.

Degree

thesis:*
Name thesis:degree_name
Ph.D.
Level thesis:degree_level
Dissertation
Discipline thesis:degree_discipline
Microbiology
Grantor
University of Illinois at Urbana-Champaign
Year dc:date
2015

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Kieke, Michele Catherine
Contributors dc:contributor
  • Kranz, David M.

Subjects

dc:subject × 1

Rights

Language dc:language
eng

Identifiers

dc:identifier.*
Identifier
(MiAaPQ)AAI9996644
OAI identifier oai:identifier
oai:www.ideals.illinois.edu:2142/86768

Chain of custody

source
Harvested from
University of Illinois - Urbana-Champaign
Base URL
www.ideals.illinois.edu/oai-pmh
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
citation

Kieke, Michele Catherine. Directed Evolution of T Cell Receptor Antagonists. Dissertation thesis, University of Illinois at Urbana-Champaign, 2015. http://hdl.handle.net/2142/86768