18O/16O‐Encoding Strategy for Microscale Stereochemical Determination of Peptidic Natural Products

The demand for more efficient methods of establishing the undetermined stereochemistries of peptidic natural products continues unabated. A new method for microscale stereochemical determination was devised by integrating solid‐phase synthesis, split‐and‐mix randomization, 18O/16O‐encoding of d/l‐co...

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Veröffentlicht in:Chemistry, an Asian journal an Asian journal, 2021-09, Vol.16 (17), p.2447-2452
Hauptverfasser: Takeuchi, Aoi, Itoh, Hiroaki, Inoue, Masayuki
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Sprache:eng
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Zusammenfassung:The demand for more efficient methods of establishing the undetermined stereochemistries of peptidic natural products continues unabated. A new method for microscale stereochemical determination was devised by integrating solid‐phase synthesis, split‐and‐mix randomization, 18O/16O‐encoding of d/l‐configurations, tandem mass spectrometry, and biological evaluation. Here we applied gramicidin A as the molecule for a blind test. Gramicidin A and its 31 diastereomers were randomly prepared in microgram scale with 18O/16O‐stereochemical encoding and subjected to MS/MS‐structural determination and cytotoxicity assay. Only the parent gramicidin A was selected from among the 32 stereoisomers, validating the high reliability of the present strategy. A novel 18O/16O‐encoding strategy for microscale stereochemical determination of peptidic natural products has been devised. The strategy integrates the one‐bead‐one‐compound (OBOC) strategy, 18O/16O‐stereochemical encoding, tandem mass (MS/MS) spectrometry, and biological evaluation. Its application enabled the correct identification of gramicidin A from 32 stereoisomers randomly prepared in microgram scale, thereby validating the high reliability.
ISSN:1861-4728
1861-471X
DOI:10.1002/asia.202100674