Publication | Open Access
Design and characterization of structured protein linkers with differing flexibilities
127
Citations
23
References
2014
Year
Protein AssemblyStructural BioinformaticsImmunologyMolecular BiologyImmunodominancePeptide ScienceAnalytical UltracentrifugationProtein FoldingEpitope AccessAntibody EngineeringProteomicsMulti-protein AssemblyMacromolecular AssembliesBiophysicsCross-linkImmunoengineeringImmunoglobulin GProtein Structure PredictionStructural BiologyBiomolecular EngineeringGly4ser Repeat LinkersNatural SciencesPeptide LibraryProtein EngineeringImmunoglobulin EStructured Protein LinkersMedicine
Engineered fusion proteins containing two or more functional polypeptides joined by a peptide or protein linker are important for many fields of biological research. The separation distance between functional units can impact epitope access and the ability to bind with avidity; thus the availability of a variety of linkers with different lengths and degrees of rigidity would be valuable for protein design efforts. Here, we report a series of designed structured protein linkers incorporating naturally occurring protein domains and compare their properties to commonly used Gly4Ser repeat linkers. When incorporated into the hinge region of an immunoglobulin G (IgG) molecule, flexible Gly4Ser repeats did not result in detectable extensions of the IgG antigen-binding domains, in contrast to linkers including more rigid domains such as β2-microglobulin, Zn-α2-glycoprotein and tetratricopeptide repeats. This study adds an additional set of linkers with varying lengths and rigidities to the available linker repertoire, which may be useful for the construction of antibodies with enhanced binding properties or other fusion proteins.
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