Glycosylation and Glycosidases-Cell & Molecular Biology
Project Number2R01GM031318-41
Former Number5R01CA014142-20
Contact PI/Project LeaderROBBINS, PHILLIPS W
Awardee OrganizationBOSTON UNIVERSITY MEDICAL CAMPUS
Description
Abstract Text
DESCRIPTION (provided by applicant): We plan to continue work in four closely
related areas: (1) chitin synthesis in yeast; (2) chitin synthesis and
glycosylation in multicellular organisms: (3) the enzymology and biology of the
hyaluronan/chitin oligosaccharide synthesizing enzyme DG42, and (4) properties
of chitin deacetylases and "antifungal" chitinases.
Yeast chitin synthase 3 (Chs3p) is targeted to the bud-neck region of the cell
where it synthesizes the chitin ring. It also functions throughout the plasma
membrane to "reinforce" the cell wall when it has been weakened. Our immediate
goals will be to compare targeting and activation of Chs3p when it is engaged
either in building the bud-neck structure or depositing chitin in the lateral
wall.
In insects, chitin is present in the cuticle and in the intestinal peritrophic
membrane. Insect genomes examined to date have two chitin synthase genes, while
most filamentous fungi have at least six. We will study the enzymology of
individual proteins that have been expressed in appropriate heterologous
systems. We will also investigate when and where the genes are transcribed and
where within cells the enzymes are localized.
From our work as well as work in other laboratories, it is clear that some
hyaluronan synthases (HAS enzymes, including DG42) are able to synthesize
either hyaluronan (a polymer of alternating glucuronic acid and
acetylglucosamine residues) or chitin oligosaccharide (containing only
acetylglucosamine) depending on conformation of the enzyme and/or incubation
conditions. In other developments, the Spaink group have shown clearly that the
chitin tetrasaccharide, and only the tetrasaccharide, is able to restore
development of the anterior-posterior axis in zebrafish inhibited with DG42
antisense RNA. We will continue our own enzymatic work and will initiate
collaborative X-ray crystallographic and biological studies.
In our fourth project, we will focus on chitin deacetylases, apparently soluble
proteins that must act on nascent chitin chains before they associate into
fibers. and on "antifungal" chitinases as potential drugs.
Public Health Relevance Statement
Data not available.
NIH Spending Category
No NIH Spending Category available.
Project Terms
Caenorhabditis elegansSaccharomycesX ray crystallographyamidohydrolasesantifungal agentscarbohydrate biosynthesiscell wallchitinenzyme mechanismenzyme structurefungal geneticsgene mutationglucuronosyltransferaseglycosidasesglycosylationisozymesprotein localizationyeast two hybrid system
No Sub Projects information available for 2R01GM031318-41
Publications
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Outcomes
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Clinical Studies
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