Literature DB >> 2447873

The detection of substructures within proteoglycan molecules. Electron-microscopic immuno-localization with the use of Protein A-gold.

J K Sheehan1, A Ratcliffe, K Oates, T E Hardingham.   

Abstract

Proteoglycan monomers from pig laryngeal cartilage were examined by electron microscopy with benzyldimethylalkylammonium chloride as the spreading agent. The proteoglycans appeared as extended molecules with a beaded structure, representing the chondroitin sulphate chains collapsed around the protein core. Often a fine filamentous tail was present at one end. Substructures within proteoglycan molecules were localized by incubation with specific antibodies followed by Protein A-gold (diameter 4 nm). After the use of an anti-(binding region) serum the Protein A-gold (typically one to three particles) bound at the extreme end of the filamentous region. A small proportion of the labelled molecules (10-15%) showed the presence of gold particles at both ends. A monoclonal antibody specific for a keratan sulphate epitope (MZ15) localized a keratan sulphate-rich region at one end of the proteoglycan, but gold particles were not observed along the extended part of the protein core. This distribution was not changed by prior chondroitin AC lyase digestion of the proteoglycan. Localization with a different monoclonal antibody to keratan sulphate (5-D-4) caused a change in the spreading behaviour of a proportion (approx. 20%) of the proteoglycan monomers that lost their beaded structure and appeared with the chondroitin sulphate chains projecting from the protein core. In these molecules the Protein A-gold localized antibody (5-D-4) along the length of the protein core whereas in those molecules with a beaded appearance it labelled only at one end. Labelling with either of the monoclonal antibodies was specific, as it was inhibited by exogenously added keratan sulphate. The differential localization achieved may reflect structural differences within the proteoglycan population involving keratan sulphate and the protein core to which it is attached. The results showed that by this technique substructures within proteoglycan molecules can be identified by Protein A-gold labelling after the use of specific monoclonal or polyclonal antibodies.

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 2447873      PMCID: PMC1148404          DOI: 10.1042/bj2470267

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  35 in total

1.  The antigenic determinants recognized by three monoclonal antibodies to keratan sulphate involve sulphated hepta- or larger oligosaccharides of the poly(N-acetyllactosamine) series.

Authors:  H Mehmet; P Scudder; P W Tang; E F Hounsell; B Caterson; T Feizi
Journal:  Eur J Biochem       Date:  1986-06-02

2.  Electron microscopy of cervical, gastric and bronchial mucus glycoproteins.

Authors:  J K Sheehan; K Oates; I Carlstedt
Journal:  Biochem J       Date:  1986-10-01       Impact factor: 3.857

3.  The specific interaction of hyaluronic acid with cartillage proteoglycans.

Authors:  T E Hardingham; H Muir
Journal:  Biochim Biophys Acta       Date:  1972-09-15

4.  Electron microscopic and physico-chemical studies on bovine nasal cartilage proteoglycan.

Authors:  P Wellauer; T Wyler; E Buddecke
Journal:  Hoppe Seylers Z Physiol Chem       Date:  1972-07

5.  Purification and properties of bacterial chondroitinases and chondrosulfatases.

Authors:  T Yamagata; H Saito; O Habuchi; S Suzuki
Journal:  J Biol Chem       Date:  1968-04-10       Impact factor: 5.157

6.  Cartilage proteoglycan binding region and link protein. Radioimmunoassays and the detection of masked determinants in aggregates.

Authors:  A Ratcliffe; T Hardingham
Journal:  Biochem J       Date:  1983-08-01       Impact factor: 3.857

7.  Proteoglycans of hyaline cartilage: Electron-microscopic studies on isolated molecules.

Authors:  J Thyberg; S Lohmander; D Heinegård
Journal:  Biochem J       Date:  1975-10       Impact factor: 3.857

8.  Separation and characterization of two populations of aggregating proteoglycans from cartilage.

Authors:  D Heinegård; J Wieslander; J Sheehan; M Paulsson; Y Sommarin
Journal:  Biochem J       Date:  1985-01-01       Impact factor: 3.857

9.  Extended and globular protein domains in cartilage proteoglycans.

Authors:  M Paulsson; M Mörgelin; H Wiedemann; M Beardmore-Gray; D Dunham; T Hardingham; D Heinegård; R Timpl; J Engel
Journal:  Biochem J       Date:  1987-08-01       Impact factor: 3.857

10.  Ultrastructure of the membrane attack complex of complement: detection of the tetramolecular C9-polymerizing complex C5b-8.

Authors:  J Tschopp; E R Podack; H J Müller-Eberhard
Journal:  Proc Natl Acad Sci U S A       Date:  1982-12       Impact factor: 11.205

View more
  4 in total

1.  Electron microscopy of cervical-mucus glycoproteins and fragments therefrom. The use of colloidal gold to make visible 'naked' protein regions.

Authors:  J K Sheehan; I Carlstedt
Journal:  Biochem J       Date:  1990-01-01       Impact factor: 3.857

2.  Structural studies of two populations of keratan sulphate chains from mature bovine articular cartilage.

Authors:  D J Thornton; H G Morris; G H Cockin; T N Huckerby; I A Nieduszynski
Journal:  Glycoconj J       Date:  1989       Impact factor: 2.916

3.  Evidence for shared epitopes within the 'naked' protein domains of human mucus glycoproteins. A study performed by using polyclonal antibodies and electron microscopy.

Authors:  J K Sheehan; R P Boot-Handford; E Chantler; I Carlstedt; D J Thornton
Journal:  Biochem J       Date:  1991-02-15       Impact factor: 3.857

4.  Structural and immunological studies of keratan sulphates from mature bovine articular cartilage.

Authors:  D J Thornton; H G Morris; G H Cockin; T N Huckerby; I A Nieduszynski; I Carlstedt; T E Hardingham; A Ratcliffe
Journal:  Biochem J       Date:  1989-05-15       Impact factor: 3.857

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.