Peptide−Sugar Ligation Catalyzed by Transpeptidase Sortase:  A Facile Approach to Neoglycoconjugate Synthesis

Glycoconjugate synthesis involving sugar and polypeptide remains a formidable challenge. Here we report a novel enzymatic method involving an unprecedented sortase-catalyzed transamidation reaction for site-specific engineering of sugars into native proteins. We show that sugars appended with a 6-am...

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Veröffentlicht in:Journal of the American Chemical Society 2008-02, Vol.130 (7), p.2132-2133
Hauptverfasser: Samantaray, Sharmishtha, Marathe, Uttara, Dasgupta, Sayani, Nandicoori, Vinay K, Roy, Rajendra P
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Sprache:eng
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Zusammenfassung:Glycoconjugate synthesis involving sugar and polypeptide remains a formidable challenge. Here we report a novel enzymatic method involving an unprecedented sortase-catalyzed transamidation reaction for site-specific engineering of sugars into native proteins. We show that sugars appended with a 6-aminohexose moiety can be efficiently ligated to peptides and proteins encoded with a LPXTG sortase recognition sequence. This robust reaction provides an elegant and simple approach for generating neoglycoproteins with an amide-linked sugar moiety at the carboxy terminus.
ISSN:0002-7863
1520-5126
DOI:10.1021/ja077358g