Peptide and Protein Synthesis by Segment Synthesis-Condensation
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 th...
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Published in: | Science (American Association for the Advancement of Science) Vol. 243; no. 4888; pp. 187 - 192 |
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Main Authors: | , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Washington, DC
The American Association for the Advancement of Science
13-01-1989
American Association for the Advancement of Science |
Subjects: | |
Online Access: | Get full text |
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Summary: | 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 T$_{1}$ and a structural analog have been synthesized with this method. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0036-8075 1095-9203 |
DOI: | 10.1126/science.2492114 |