Publication | Closed Access
Design and Chemical Synthesis of a Homogeneous Polymer-Modified Erythropoiesis Protein
312
Citations
23
References
2003
Year
Tissue EngineeringEngineering166-Amino-acid Polypeptide ChainPeptide EngineeringMolecular BiologyChemical BiologyProteomicsBiomimetic PolymerFunctional ModificationProtein FunctionBiochemistryBiomolecular EngineeringSynthetic Erythropoiesis ProteinNatural SciencesPeptide LibrarySynthetic BiologyTotal Chemical SynthesisPeptide SynthesisProtein Engineering
We report the design and total chemical synthesis of "synthetic erythropoiesis protein" (SEP), a 51-kilodalton protein-polymer construct consisting of a 166-amino-acid polypeptide chain and two covalently attached, branched, and monodisperse polymer moieties that are negatively charged. The ability to control the chemistry allowed us to synthesize a macromolecule of precisely defined covalent structure. SEP was homogeneous as shown by high-resolution analytical techniques, with a mass of 50,825 +/-10 daltons by electrospray mass spectrometry, and with a pI of 5.0. In cell and animal assays for erythropoiesis, SEP displayed potent biological activity and had significantly prolonged duration of action in vivo. These chemical methods are a powerful tool in the rational design of protein constructs with potential therapeutic applications.
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