| Literature DB >> 2492114 |
E T Kaiser1, H Mihara, G A Laforet, J W Kelly, L Walters, M A Findeis, T Sasaki.
Abstract
The chemical synthesis of biologically active peptides and polypeptides can be achieved by using a convergent strategy of condensing protected peptide segments to form the desired molecule. An oxime support increases the ease with which intermediate protected peptides can be synthesized and makes this approach useful for the synthesis of peptides in which secondary structural elements have been redesigned. The extension of these methods to large peptides and proteins, for which folding of secondary structures into functional tertiary structures is critical, is discussed. Models of apolipoproteins, the homeo domain from the developmental protein encoded by the Antennapedia gene of Drosophila, a part of the Cro repressor, and the enzyme ribonuclease T1 and a structural analog have been synthesized with this method.Entities:
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Year: 1989 PMID: 2492114 DOI: 10.1126/science.2492114
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728