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Synthetic Erythropoietic Proteins: Tuning Biological Performance by Site-Specific Polymer Attachment

Authors :
E. Neil Cagle
Maia Carnevali
John W. Adamson
Vincent Gueriguian
Carlos E. Bozzini
Gerd G. Kochendoerfer
Sonya Cressman
James A. Bradburne
Ada Kung
M. Con Wiedeke
Heather Porter
Laura Savatski
Stephen M. Stratton
Feng Mao
Haiyan Shao
Donald W. Low
Stephen B. H. Kent
Shiah-Yun Chen
Peter J. Keogh
Hal S. Beilan
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.

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