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Síntese em Fase Sólida de um funcionalizada Bis Peptide-Usando o "Safety Catch" Metodologia
JoVE Journal
Biology
This content is Free Access.
JoVE Journal Biology
Solid Phase Synthesis of a Functionalized Bis-Peptide Using “Safety Catch” Methodology
DOI:

11:42 min

May 15, 2012

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Chapters

  • 00:05Title
  • 01:55Loading of First Bis-Peptide, Deprotection of First Bis-Peptide, and Simultaneous Resin Capping
  • 03:43Coupling Tert-butyl Carbamate (Boc)/tert-butyl Ester(tBu)-protected Functionalized Bis-Amino Acid
  • 05:21Deprotection of Boc/tBu-protected Functionalized Bis-Amino Acid, Deprotection of Fmoc, and Acylation of the First Bis-Amino Acid
  • 06:55Removal of the Boc Group from the Resin Bound Amino Acid and Cleavage from the Resin
  • 07:56Assessment Methods
  • 09:51Results: Analysis by Liquid Chromatography and Mass Spectroscopy
  • 10:36Conclusion

Summary

Automatic Translation

A síntese de péptidos em fase sólida eficiente de um trímero bis péptido-funcionalizado utilizando um "fecho de segurança" procedimento de clivagem a partir de resina de HMBA é descrito.

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