Supramolecular Protein Engineering

Autor: Nelson B. Phillips, Michael A. Weiss, Qing Xin Hua, Faramarz Ismail-Beigi, Jonathan Whittaker, Zhu Li Wan, Kun Huang, Linda Whittaker, Shi Quan Hu
Rok vydání: 2010
Předmět:
Zdroj: Journal of Biological Chemistry. 285:11755-11759
ISSN: 0021-9258
DOI: 10.1074/jbc.c110.105825
Popis: Bottom-up control of supramolecular protein assembly can provide a therapeutic nanobiotechnology. We demonstrate that the pharmacological properties of insulin can be enhanced by design of “zinc staples” between hexamers. Paired (i, i+4) His substitutions were introduced at an α-helical surface. The crystal structure contains both classical axial zinc ions and novel zinc ions at hexamer-hexamer interfaces. Although soluble at pH 4, the combined electrostatic effects of the substitutions and bridging zinc ions cause isoelectric precipitation at neutral pH. Following subcutaneous injection in a diabetic rat, the analog effected glycemic control with a time course similar to that of long acting formulation Lantus®. Relative to Lantus, however, the analog discriminates at least 30-fold more stringently between the insulin receptor and mitogenic insulin-like growth factor receptor. Because aberrant mitogenic signaling may be associated with elevated cancer risk, such enhanced specificity may improve safety. Zinc stapling provides a general strategy to modify the pharmacokinetic and biological properties of a subcutaneous protein depot.
Databáze: OpenAIRE