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Synthesis of Pseudooligosaccharides Related to the Capsular Phosphoglycan of Haemophilus influenzae Type a.


ABSTRACT: Synthesis of spacer-armed pseudodi-, pseudotetra-, and pseudohexasaccharides related to the capsular phosphoglycan of Haemophilus influenzae type a, the second most virulent serotype of H. influenzae (after type b), was performed for the first time via iterative chain elongation using H-phosphonate chemistry for the formation of inter-unit phosphodiester bridges. These compounds were prepared for the design of neoglycoconjugates, as exemplified by the transformation of the obtained pseudohexasaccharide derivative into a biotinylated glycoconjugate suitable for use in immunological studies, particularly in diagnostic screening systems as a coating antigen for streptavidin-coated plates and chip slides.

SUBMITTER: Kamneva AA 

PROVIDER: S-EPMC10419796 | biostudies-literature | 2023 Jul

REPOSITORIES: biostudies-literature

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Synthesis of Pseudooligosaccharides Related to the Capsular Phosphoglycan of <i>Haemophilus influenzae</i> Type <i>a</i>.

Kamneva Anastasia A AA   Yashunsky Dmitry V DV   Khatuntseva Elena A EA   Nifantiev Nikolay E NE  

Molecules (Basel, Switzerland) 20230727 15


Synthesis of spacer-armed pseudodi-, pseudotetra-, and pseudohexasaccharides related to the capsular phosphoglycan of <i>Haemophilus influenzae</i> type <i>a</i>, the second most virulent serotype of <i>H. influenzae</i> (after type <i>b</i>), was performed for the first time via iterative chain elongation using H-phosphonate chemistry for the formation of inter-unit phosphodiester bridges. These compounds were prepared for the design of neoglycoconjugates, as exemplified by the transformation o  ...[more]

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