Menegatti, Stefano et al. published their research in Biotechnology and Bioengineering in 2013 |CAS: 79642-50-5

The Article related to mrna display library cyclic peptide fc binding antibody purification, Immunochemistry: Methods (Including Analysis) and other aspects.Computed Properties of 79642-50-5

Menegatti, Stefano; Hussain, Mahmud; Naik, Amith D.; Carbonell, Ruben G.; Rao, Balaji M. published an article in 2013, the title of the article was mRNA display selection and solid-phase synthesis of Fc-binding cyclic peptide affinity ligands.Computed Properties of 79642-50-5 And the article contains the following content:

Cyclic peptides are attractive candidates for synthetic affinity ligands due to their favorable properties, such as resistance to proteolysis, and higher affinity and specificity relative to linear peptides. Here we describe the discovery, synthesis and characterization of novel cyclic peptide affinity ligands that bind the Fc portion of human IgG (IgG; hFc). We generated an mRNA display library of cyclic pentapeptides wherein peptide cyclization was achieved with high yield and selectivity, using a solid-phase crosslinking reaction between two primary amine groups, mediated by a homobifunctional linker. Subsequently, a pool of cyclic peptide binders to hFc was isolated from this library and chromatog. resins incorporating the selected cyclic peptides were prepared by on-resin solid-phase peptide synthesis and cyclization. Significantly, this approach results in resins that are resistant to harsh basic conditions of column cleaning and regeneration. Further studies identified a specific cyclic peptide-cyclo[Link-M-WFRHY-K]-as a robust affinity ligand for purification of IgG from complex mixtures The cyclo[Link-M-WFRHY-K] resin bound selectively to the Fc fragment of IgG, with no binding to the Fab fragment, and also bound Igs from a variety of mammalian species. Notably, while the recovery of IgG using the cyclo[Link-M-WFRHY-K] resin was comparable to a Protein A resin, elution of IgG could be achieved under milder conditions (pH 4 vs. pH 2.5). Thus, cyclo[Link-M-WFRHY-K] is an attractive candidate for developing a cost-effective and robust chromatog. resin to purify monoclonal antibodies (mAbs). Finally, our approach can be extended to efficiently generate and evaluate cyclic peptide affinity ligands for other targets of interest. The experimental process involved the reaction of Bis(2,5-dioxopyrrolidin-1-yl) glutarate(cas: 79642-50-5).Computed Properties of 79642-50-5

The Article related to mrna display library cyclic peptide fc binding antibody purification, Immunochemistry: Methods (Including Analysis) and other aspects.Computed Properties of 79642-50-5

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