An efficient, general, and racemization free method of covalently attaching No-F'KKXZ protected amino acids to solid supports for peptide synthesis is described. The process involves the preparation of 2,4-dichlorophenyl-Na-Fmoc-aminoaql-4-oxyn~sthylphenoxy acetates which can be used to directly and
Use of Marfey's reagent to quantitate racemization upon anchoring of amino acids to solid supports for peptide synthesis
β Scribed by J. Gordon Adamson; Thang Hoang; Anna Crivici; Gilles A. Lajoie
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- English
- Weight
- 517 KB
- Volume
- 202
- Category
- Article
- ISSN
- 0003-2697
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β¦ Synopsis
A chromatographic assay has been developed to quantitate racemization occurring during attachment of protected amino acids to peptide synthesis resins. Acidolytic cleavage of deprotected amino acids from supports and subsequent derivatization with 1-fluoro-2,4-dinitrophenyl-5-L-alanine amide (Marfey's reagent) gave diastereomers separable by reverse-phase HPLC using aqueous acetonitrile. The assay is reliable to 0.1% racemate with a detection limit of approximately 100 pmol. The technique was applied to several acid-labile resins and was used to evaluate the racemizing characteristics of various anchoring methods.
π SIMILAR VOLUMES
The cesium salts of N -9-fluorenylmethyloxycarbonyl (Fmoc) amino acids couple smoothly to new chloro derivatives of alkoxy benryl alcohol resins. While high loading is attained under mild reaction conditions racemization can be suppressed even with Cys and His derivatives.