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http://purl.uniprot.org/citations/34877503http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/34877503http://www.w3.org/2000/01/rdf-schema#comment"Bispecific antibodies (Bispecifics) demonstrate exceptional clinical potential to address some of the most complex diseases. However, Bispecific production in a single cell often requires the correct pairing of multiple polypeptide chains for desired assembly. This is a considerable hurdle that hinders the development of many immunoglobulin G (IgG)-like bispecific formats. Our approach focuses on the rational engineering of charged residues to facilitate the chain pairing of distinct heavy chains (HC). Here, we deploy structure-guided protein design to engineer charge pair mutations (CPMs) placed in the CH3-CH3' interface of the fragment crystallizable (Fc) region of an antibody (Ab) to correctly steer heavy chain pairing. When used in combination with our stable effector functionless 2 (SEFL2.2) technology, we observed high pairing efficiency without significant losses in expression yields. Furthermore, we investigate the relationship between CPMs and the sequence diversity in the parental antibodies, proposing a rational strategy to deploy these engineering technologies."xsd:string
http://purl.uniprot.org/citations/34877503http://purl.org/dc/terms/identifier"doi:10.1016/j.isci.2021.103447"xsd:string
http://purl.uniprot.org/citations/34877503http://purl.uniprot.org/core/author"Li D."xsd:string
http://purl.uniprot.org/citations/34877503http://purl.uniprot.org/core/author"Zhang J."xsd:string
http://purl.uniprot.org/citations/34877503http://purl.uniprot.org/core/author"Wang Z."xsd:string
http://purl.uniprot.org/citations/34877503http://purl.uniprot.org/core/author"Whittington D.A."xsd:string
http://purl.uniprot.org/citations/34877503http://purl.uniprot.org/core/author"Garces F."xsd:string
http://purl.uniprot.org/citations/34877503http://purl.uniprot.org/core/author"Mohr C."xsd:string
http://purl.uniprot.org/citations/34877503http://purl.uniprot.org/core/author"Estes B."xsd:string
http://purl.uniprot.org/citations/34877503http://purl.uniprot.org/core/author"Gong D."xsd:string
http://purl.uniprot.org/citations/34877503http://purl.uniprot.org/core/author"Sudom A."xsd:string
http://purl.uniprot.org/citations/34877503http://purl.uniprot.org/core/author"Li V."xsd:string
http://purl.uniprot.org/citations/34877503http://purl.uniprot.org/core/author"Riley T.P."xsd:string
http://purl.uniprot.org/citations/34877503http://purl.uniprot.org/core/author"Shi S.D."xsd:string
http://purl.uniprot.org/citations/34877503http://purl.uniprot.org/core/date"2021"xsd:gYear
http://purl.uniprot.org/citations/34877503http://purl.uniprot.org/core/name"iScience"xsd:string
http://purl.uniprot.org/citations/34877503http://purl.uniprot.org/core/pages"103447"xsd:string
http://purl.uniprot.org/citations/34877503http://purl.uniprot.org/core/title"Next generation Fc scaffold for multispecific antibodies."xsd:string
http://purl.uniprot.org/citations/34877503http://purl.uniprot.org/core/volume"24"xsd:string
http://purl.uniprot.org/citations/34877503http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/34877503
http://purl.uniprot.org/citations/34877503http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/34877503
http://purl.uniprot.org/uniprot/#_P01857-mappedCitation-34877503http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34877503
http://purl.uniprot.org/uniprot/#_P01859-mappedCitation-34877503http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34877503
http://purl.uniprot.org/uniprot/P01857http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/34877503