File:Peptide Synthesis.png
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![File:Peptide Synthesis.png](https://upload.wikimedia.org/wikipedia/commons/thumb/b/bb/Peptide_Synthesis.png/800px-Peptide_Synthesis.png?20091129202036)
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Summary
[edit]DescriptionPeptide Synthesis.png |
English: Solid-phase peptide synthesis |
Date | |
Source | Own, Adobe Illustrator |
Author | Dan Cojocari |
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Annotations InfoField | This image is annotated: View the annotations at Commons |
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Rink Linker that connects the solid resin to the peptide being built
3
335
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693
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Solid resin for peptide synthesis
1063
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The first amino acid (side group R1) conjugated to an Fmoc group that protects the amino end.
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851
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Acid catalyzed (Trifluoroacetic acid) decoupling of the finished peptide and the linker. The linker ends up with and -OH group, instead of the initial -NH2.
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Basic conditions required in order to keep -NH2 ,not -NH3+
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Mechanism of acid-catalyzed uncoupling.
File history
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Date/Time | Thumbnail | Dimensions | User | Comment | |
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current | 20:20, 29 November 2009 | ![]() | 2,701 × 1,215 (249 KB) | Dancojocari (talk | contribs) | Fmoc structure correction |
19:54, 29 November 2009 | ![]() | 2,701 × 1,180 (224 KB) | Dancojocari (talk | contribs) | {{Information |Description={{en|1=Solid-phase peptide synthesis}} |Source=Own, Adobe Illustrator |Author=Dancojocari |Date=2009-11-29 |Permission= |other_versions= }} |
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