Proteoglycans are ubiquitous components of connective tissues. They often occur as major components of the extra-cellular matrix of these tissues. Cartilage proteoglycans have been the most thoroughly studied and they have served as a useful model for examining proteoglycan structure and function in other more complex connective tissue matrices. Detailed analysis of proteoglycan structure by conventional biochemical procedures has been complicated by the inherent heterogeneity and polydisperisty of the proteoglycans themselves. Immunological methods offer the possibililty of raising antibodies which specifically recognize different antigenic determinants present on proteoglycans and link protein. The recent introduction of monoclonal antibody procedures has offered the possiblity of producing antibodies which specifically recognize structural and functional antigenic determinants on biological macromolecules. In this proposal we plan to produce and characterize monoclonl antibodies that recognize specific determinants on proteoglycan and link protein. The specificity of the antibodies will be determined using biochemical methods, and in immunoassay procedures. Specific antibodies will be applied to problems of quantitating, identifying, purifying and determining the tissue distribution of proteoglycan and link protein. Both immunochemical studies on isolated material and immunohistochemical procedures will be employed. A major objective of this proposal is to use specific monoclonal antibodies as a means of characterizing and purifying peptide fragments of link protein and proteoglycan. These peptides will be used in the determination of the amino acid sequences (primary structure) of link protein and lproteoglycan. In addition, antibodies recognizing functional aspects of proteoglycan and link protein interactions will be used instudies determining structure function relationships involved in proteoglycan aggregate formation. A longer term objective is to extend these studies to gain a better understanding of proteoglycan metabolism in other more complex connective tissues. These studies will increase our knowledge of connective tissue function in normal conditions and in disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis, Diabetes, Digestive and Kidney Diseases (NIADDK)
Type
Research Project (R01)
Project #
5R01AM032666-03
Application #
3152580
Study Section
Pathobiochemistry Study Section (PBC)
Project Start
1983-09-01
Project End
1986-08-31
Budget Start
1985-09-01
Budget End
1986-08-31
Support Year
3
Fiscal Year
1985
Total Cost
Indirect Cost
Name
West Virginia University
Department
Type
School of Medicine & Dentistry
DUNS #
191510239
City
Morgantown
State
WV
Country
United States
Zip Code
26506
Funderburgh, J L; Caterson, B; Conrad, G W (1987) Distribution of proteoglycans antigenically related to corneal keratan sulfate proteoglycan. J Biol Chem 262:11634-40
DiFabio, J L; Pearce, R H; Caterson, B et al. (1987) The heterogeneity of the non-aggregating proteoglycans of the human intervertebral disc. Biochem J 244:27-33
Oguri, K; Okayama, E; Caterson, B et al. (1987) Isolation, characterization, and localization of glycosaminoglycans in rabbit bone marrow. Blood 70:501-10
Miller, M R; Heyneman, C; Walker, S et al. (1986) Interaction of monoclonal antibodies directed against bromodeoxyuridine with pyrimidine bases, nucleosides, and DNA. J Immunol 136:1791-5
Funderburgh, J L; Caterson, B; Conrad, G W (1986) Keratan sulfate proteoglycan during embryonic development of the chicken cornea. Dev Biol 116:267-77
Caterson, B; Baker, J R; Christner, J E et al. (1985) Monoclonal antibodies as probes for determining the microheterogeneity of the link proteins of cartilage proteoglycan. J Biol Chem 260:11348-56
Mort, J S; Caterson, B; Poole, A R et al. (1985) The origin of human cartilage proteoglycan link-protein heterogeneity and fragmentation during aging. Biochem J 232:805-12
Fife, R S; Caterson, B; Myers, S L (1985) Identification of link proteins in canine synovial cell cultures and canine articular cartilage. J Cell Biol 100:1050-5