The applicant's study of the cell cycle regulatory protein FP21 in the cellular slime mold Dictyostelium discoideum has led to the discovery of a novel pentasaccharide attached to a hydroxylated Pro-residue at position 143. This is a bulky substituent to be located on a highly conserved surface of a protein. It is also an unusual structure to find on a cytoplasmic/nuclear protein, as Pro hydroxylation and complex glycosylation are usually thought to be confined to the secretory pathway of the cell. The applicant's long term goals are to understand how this complex postranslational covalent modification, which cannot be predicted from cDNA sequence data, affects the function of FP21 and other proteins on which it presumably occurs. This project will focus on how the pentasaccharide is biosynthesized, initially using FP21 as a substrate to identify potentially key enzymes in the pathway. This will involve first establishing the specificity of the enzymes which govern its biosynthesis by completing the structure determination of the HyPro pentasaccharide (aim #1). This will be followed by purification of 2 early enzyme activities of the pathway, the ProHydroxylase and the GalNAcTransferase, and examining their substrate specificity and kinetic constants (aim#2). This approach is expected to identify candidate enzymes for the pathway, suggest the cellular compartment in which each operates, and the basis for its substrate recognition. Cloning cDNAs for these 2 enzymes and the cFucTase (aim#3) will lead to the primary structure of each enzyme protein, which will independently address their compartmentalization, suggest an evolutionary relationship with corresponding known enzymes in the secretory pathway, and provide tools for critical manipulations in the later aims. The sufficiency of each enzyme polypeptide for catalyzing its proposed step of the pathway will be established by expression of its cDNA in a heterologous system followed by enzymatic assay (aim #4). Finally, the necessity of the enzyme polypeptide for execution of the pathway step in vivo, and its co-compartmentalization with FP21, will be addressed by genetic disruption of the enzyme genes and expression of FP21 in the secretory pathway, respectively in Dictyostelium (aim#5). In addition to firmly establishing the basic principles by which the HyPro pathway initially targets and modifies FP21, the results will provide an important gateway through which we can detect this pathway in other organisms, regardless of whether FP21 is glycosylated in the particular cell or tissue type examined. The tools developed will permit future dissection of the role of complex glycosylation of cytoplasmic/nuclear proteins which may, based on the phenotype of FP21 and glycosylation mutants, be fundamentally important for cell proliferation and metabolism.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM037539-11
Application #
6329673
Study Section
Pathobiochemistry Study Section (PBC)
Program Officer
Marino, Pamela
Project Start
1986-07-01
Project End
2001-11-30
Budget Start
2000-12-01
Budget End
2001-11-30
Support Year
11
Fiscal Year
2001
Total Cost
$199,639
Indirect Cost
Name
University of Florida
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
073130411
City
Gainesville
State
FL
Country
United States
Zip Code
32611
Gas-Pascual, Elisabet; Ichikawa, Hiroshi Travis; Sheikh, Mohammed Osman et al. (2018) CRISPR/Cas9 and glycomics tools for Toxoplasma glycobiology. J Biol Chem :
Xu, Xianzhong; Eletsky, Alexander; Sheikh, M Osman et al. (2018) Glycosylation Promotes the Random Coil to Helix Transition in a Region of a Protist Skp1 Associated with F-Box Binding. Biochemistry 57:511-515
Sheikh, M Osman; Halmo, Stephanie M; Patel, Sneha et al. (2017) Rapid screening of sugar-nucleotide donor specificities of putative glycosyltransferases. Glycobiology 27:206-212
Sheikh, M Osman; Thieker, David; Chalmers, Gordon et al. (2017) O2 sensing-associated glycosylation exposes the F-box-combining site of the Dictyostelium Skp1 subunit in E3 ubiquitin ligases. J Biol Chem 292:18897-18915
Summers, Jody A; Harper, Angelica R; Feasley, Christa L et al. (2016) Identification of Apolipoprotein A-I as a Retinoic Acid-binding Protein in the Eye. J Biol Chem 291:18991-9005
West, Christopher M; Blader, Ira J (2015) Oxygen sensing by protozoans: how they catch their breath. Curr Opin Microbiol 26:41-7
Feasley, Christa L; van der Wel, Hanke; West, Christopher M (2015) Evolutionary diversity of social amoebae N-glycomes may support interspecific autonomy. Glycoconj J 32:345-59
Sheikh, M Osman; Xu, Yuechi; van der Wel, Hanke et al. (2015) Glycosylation of Skp1 promotes formation of Skp1-cullin-1-F-box protein complexes in dictyostelium. Mol Cell Proteomics 14:66-80
Chinoy, Zoeisha S; Schafer, Christopher M; West, Christopher M et al. (2015) Chemical Synthesis of a Glycopeptide Derived from Skp1 for Probing Protein Specific Glycosylation. Chemistry 21:11779-87
Sheikh, M Osman; Schafer, Christopher M; Powell, John T et al. (2014) Glycosylation of Skp1 affects its conformation and promotes binding to a model f-box protein. Biochemistry 53:1657-69

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