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    <identifier identifierType="DOI">10.26249/FK2/NPX7DU</identifier>
    <creators><creator><creatorName>Pollmann, Christoph</creatorName><nameIdentifier schemeURI="https://orcid.org/" nameIdentifierScheme="ORCID">0000-0002-1473-0288</nameIdentifier><affiliation>(Osnabrück University)</affiliation></creator></creators>
    <titles>
        <title>A Strategy to Design Protein-based Antagonists Against Type I Cytokine Receptors</title>
    </titles>
    <publisher>osnaData</publisher>
    <publicationYear>2024</publicationYear>
    <resourceType resourceTypeGeneral="Dataset"/>
    
    <descriptions>
        <description descriptionType="Abstract">Excessive cytokine signaling resulting from dysregulation of a cytokine or its receptor can be a main driver of cancer, autoimmune or hematopoietic disorders. Here we leverage protein design to create tailored cytokine receptor blockers with idealized properties. Specifically, we aimed to tackle the granulocyte-colony stimulating factor receptor (G-CSFR), a mediator of different types of leukemia and autoinflammatory diseases. By modifying designed G-CSFR binders, we engineered hyper-stable proteins that function as nanomolar signaling antagonists. X-ray crystallography showed atomic-level agreement with the experimental structure of an exemplary design. Furthermore, the most potent design blocks G-CSFR in acute myeloid leukemia cells and primary hematopoietic stem cells. Thus, the resulting designs can be used for inhibiting or homing to G-CSFR-expressing cells. Our work also demonstrates that designed cytokine mimics can be used to derive non-activating variants for tackling a range of cytokine receptors.</description>
    </descriptions>
    <contributors><contributor contributorType="ContactPerson"><contributorName>Pollmann, Christoph</contributorName><affiliation>(Osnabrück University)</affiliation></contributor></contributors>
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