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Synthetic Erythropoietic Proteins: Tuning Biological Performance by Site-Specific Polymer Attachment
- Source :
- Chemistry & Biology. 12(3):371-383
- Publication Year :
- 2005
- Publisher :
- Elsevier BV, 2005.
-
Abstract
- SummaryChemical synthesis in combination with precision polymer modification allows the systematic exploration of the effect of protein properties, such as charge and hydrodynamic radius, on potency using defined, homogeneous conjugates. A series of polymer-modified synthetic erythropoiesis proteins were constructed that had a polypeptide chain similar to the amino acid sequence of human erythropoietin but differed significantly in the number and type of attached polymers. The analogs differed in charge from +5 to −26 at neutral pH and varied in molecular weight from 30 to 54 kDa. All were active in an in vitro cell proliferation assay. However, in vivo potency was found to be strongly dependent on overall charge and size. The trends observed in this study may serve as starting points for the construction of more potent synthetic EPO analogs in the future.
- Subjects :
- Hydrodynamic radius
Polymers
Molecular Sequence Data
Clinical Biochemistry
Chemical synthesis
Biochemistry
Mice
In vivo
Drug Discovery
Animals
Humans
Erythropoiesis
Amino Acid Sequence
Binding site
Erythropoietin
Peptide sequence
Molecular Biology
Cell Proliferation
chemistry.chemical_classification
Pharmacology
Binding Sites
Dose-Response Relationship, Drug
Chemistry
Proteins
General Medicine
Polymer
In vitro
Rats
Macaca fascicularis
Molecular Medicine
Conjugate
Subjects
Details
- ISSN :
- 10745521
- Volume :
- 12
- Issue :
- 3
- Database :
- OpenAIRE
- Journal :
- Chemistry & Biology
- Accession number :
- edsair.doi.dedup.....9455f5c2578524928fd3f5cbf800ce2c
- Full Text :
- https://doi.org/10.1016/j.chembiol.2005.01.017