Programmable Design of Protein Interaction Specificity and Logic Gates

dc.contributor.advisorBaker, David
dc.contributor.advisorDiMaio, Frank
dc.contributor.authorChen, Zibo
dc.date.accessioned2019-02-22T17:02:50Z
dc.date.available2019-02-22T17:02:50Z
dc.date.issued2019-02-22
dc.date.submitted2018
dc.descriptionThesis (Ph.D.)--University of Washington, 2018
dc.description.abstractThe binding specificity of DNA molecules is straightforward: adenine binds thymine, and cytosine binds guanine. This simple encoding of specificity enables the binding between two DNA molecules to be modularly and programmatically designed. Proteins do not have such straightforward encoding of binding specificity, but could one design for it? This thesis argues such feature can indeed be designed into proteins. I first show orthogonal heterodimers can be designed modularly and programmably to have DNA-like specificity, followed by showing such principles open the door to algorithmic self-assembly of proteins into 2D lattices.
dc.embargo.termsOpen Access
dc.format.mimetypeapplication/pdf
dc.identifier.otherChen_washington_0250E_19412.pdf
dc.identifier.urihttp://hdl.handle.net/1773/43306
dc.language.isoen_US
dc.rightsCC BY-NC-SA
dc.subjectBiophysics
dc.subjectComputational biology
dc.subjectStructural biology
dc.subjectBiochemistry
dc.subject.otherBiological chemistry
dc.titleProgrammable Design of Protein Interaction Specificity and Logic Gates
dc.typeThesis

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