Copolypeptides biomimetic

Cha JN, Stucky GD, Morse DE, Deming TJ (2000) Biomimetic synthesis of ordered silica structures mediated by block copolypeptides. Nature 403 289-292... 

Abstract The aggregation behaviour of biomimetic polypeptide hybrid copolymers and copolypeptides is here reviewed with a particular eye on the occurrence of secondary structure effects. Structure elements like a-helix or / -sheet can induce a deviation from the classical phase behaviour and promote the formation of vesicles or hierarchical superstructures with ordering in the length-scale of microns. Polypeptide copolymers are therefore considered as models to study self-assembly processes in biological systems. In addition, they offer a great potential for a production of novel advanced materials and colloids. 

There has been a report of enzyme-like activity in a block copolypeptide, which enhances the rate of hydrolysis of tetraethoxysilane (TEOS, a standard reagent in sol-gel chemistry) as a suspension in water. If this block structure is a sequence of units of a hydrophilic amino followed by units of a hydrophobic amino acid, it would be expected to be active at a water-solvent interface. The morphology of the silica that forms is dependent on the structure of the copolymer. This system is biomimetic both in the sense of employing a polypeptide catalyst and in the sense of it functioning in a multiphase system, since biological processes rarely occur in homogeneous solutions. 

Jan, J.-S. and Shantz, D.F. (2007) Biomimetic silica formation effect of block copolypeptide chemistry and solution conditions on silica nanostructure. Advanced Materials, 19, 2951-6. 

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