Design of De Novo Mimetic Protein of Interleukin-21

dc.contributor.advisorBaker, David
dc.contributor.advisorKing, Neil
dc.contributor.authorChun, Jung Ho
dc.date.accessioned2024-02-12T23:38:54Z
dc.date.issued2024-02-12
dc.date.submitted2023
dc.descriptionThesis (Ph.D.)--University of Washington, 2023
dc.description.abstractInterleukin-21 (IL-21) is crucial in coordinating immune cells and has pleiotropic effects in their immune responses. It has established clinical anti-tumor activity in many cancer models. Despite its efficacy, its therapeutic window has been limited due to its systemic toxicity and poor protein engineerability, resulting in the molecule with suboptimal biodistribution and pharmacokinetic properties. In addition, the limited cross-reactivity of human IL-21 in mice complicates the use of animal models to study the toxicity and activity of candidate IL-21 therapeutics. Here, we created de novo IL-21 mimetic proteins that can fully recapitulate its interaction with receptors and the biology of native IL-21 in both humans and mice.
dc.embargo.lift2026-02-11T23:38:54Z (extended from original one year embargo)
dc.embargo.termsDelay release for 2 years -- then make Open Access
dc.format.mimetypeapplication/pdf
dc.identifier.otherChun_washington_0250E_26420.pdf
dc.identifier.urihttp://hdl.handle.net/1773/51098
dc.language.isoen_US
dc.rightsnone
dc.subjectBiochemistry
dc.subjectBiophysics
dc.subjectBioengineering
dc.subject.otherBiological chemistry
dc.titleDesign of De Novo Mimetic Protein of Interleukin-21
dc.typeThesis

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