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Synthesis of Proteins by Native Chemical Ligation Using Fmoc-Based Chemistry

โœ Scribed by Julio A. Camarero; Alexander R. Mitchell

Publisher
John Wiley and Sons
Year
2006
Weight
8 KB
Volume
37
Category
Article
ISSN
0931-7597

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๐Ÿ“œ SIMILAR VOLUMES

Peptide thioester preparation by Fmoc so
Peptide thioester preparation by Fmoc solid phase peptide synthesis for use in native chemical ligation
โœ Andrew B. Clippingdale; Colin J. Barrow; John D. Wade ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 135 KB ๐Ÿ‘ 2 views

Established methodology for the preparation of peptide thioesters requires the use of t-butoxycarbonyl chemistry owing to the lability of thioester linkers to the nucleophilic reagents used in Fmoc solid phase peptide synthesis. Both the greater ease of use and the broad applicability of the method

Synthesis of a three zinc finger protein
Synthesis of a three zinc finger protein, Zif268, by native chemical ligation
โœ Gangamani S. Beligere; Philip E. Dawson ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› Wiley (John Wiley & Sons) ๐ŸŒ English โš– 99 KB ๐Ÿ‘ 2 views

Protein synthesis by native chemical ligation has been an effective approach for the synthesis of proteins of moderate size. The utility of this approach for protein synthesis is demonstrated by the synthesis of a transcription factor, Zif 268 that contains three zinc finger domains. This synthesis