Journal article
Separation of fast from slow anabolism by site-specific PEGylation of insulin-like growth factor I (IGF-I)
F Metzger, W Sajid, S Saenger, C Staudenmaier, C Van Der Poel, B Sobottka, A Schuler, M Sawitzky, R Poirier, D Tuerck, E Schick, A Schaubmar, F Hesse, K Amrein, H Loetscher, GS Lynch, A Hoeflich, P De Meyts, HJ Schoenfeld
Journal of Biological Chemistry | AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC | Published : 2011
Abstract
Insulin-like growth factor I (IGF-I) has important anabolic and homeostatic functions in tissues like skeletal muscle, and a decline in circulating levels is linked with catabolic conditions. Whereas IGF-I therapies for musculoskeletal disorders have been postulated, dosing issues and disruptions of the homeostasis have so far precluded clinical application. We have developed a novel IGF-I variant by site-specific addition of polyethylene glycol (PEG) to lysine 68 (PEG-IGF-I). In vitro, this modification decreased the affinity for the IGF-I and insulin receptors, presumably through decreased association rates, and slowed down the association to IGF-I-binding proteins, selectively limiting fa..
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Funding Acknowledgements
This work was supported in part by a Roche Postdoctoral Fellowship (to C. v. d. P.).