Evolution versus design: template-directed self-assembly of peptides to artificial proteins (TASP)

• Published in: Chimia, vol. 54, num. 10, p. 552-557
• Publication date: 2000

A review with twenty-nine refs. on the authors' current research. Protein design and mimicry combines elements of synthetic org. chem. with structural and functional aspects of biol. relevance in a unique way. Due to progress in this interdisciplinary research field, access to mols. featuring some essential properties of native proteins appears to be within reach, enabling the complex mechanisms in mol. recognition processes to be deciphered. Since its introduction by the authors, the template approach in protein de novo design (Template Assembled Synthetic Proteins, TASP) has experienced a broad conceptual diversification. Starting from today's state-of-the-art in protein design, we present here some ongoing work in the Lausanne labs. focusing on the use of regioselectively addressable templates and TASP scaffolds for addressing fundamental questions in peptide assembly, protein folding and mimicry. It is shown that the developed concepts can ideally reconcile evolutionary and rational design principles for creating mols. of biol. and therapeutic interest. [on SciFinder (R)]

Reference

• LCBP-ARTICLE-2000-002

Record created on 2006-02-09, modified on 2016-08-08