Literature DB >> 2413214

An X-ray diffraction analysis of rat tail tendons treated with Cupromeronic Blue.

K M Meek, J E Scott, C Nave.   

Abstract

Cupromeronic Blue was used to stain selectively the proteoglycans in rat tail tendons under 'critical electrolyte' conditions. Earlier electron microscopical observations indicated that at least one type of proteoglycan filament is associated with tendon collagen fibrils at the positive staining band 'd'. To ensure that this was not an artefact caused by specimen preparation or the subsequent positive staining of the collagen fibrils, we have analysed low angle meridional diffraction patterns from stained but not dehydrated, embedded or counterstained tissues. Axial electron density profiles of Cupromeronic Blue-stained compared with unstained rat tail tendons revealed the axial locations and relative amounts of dye in both mature and young wet specimens. In mature tendons, the difference electron density profile contained a broad peak centred near residue 180 along the 234-residue D-period. This corresponds to the electron-optical staining band 'd'. In young tendons a similar distribution of stain was observed although in this case there was evidence of a doublet of peaks, one centred near residue 182 (band 'd') and the other near residue 165 (midway between bands d and e1). The wet proteoglycan--Cupromeronic Blue complexes distribute over about 30 nm along the collagen fibril axis. Comparison with the images of filaments seen in the electron microscope suggests that the dye complexes collapse significantly on dehydration and embedding.

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Year:  1985        PMID: 2413214     DOI: 10.1111/j.1365-2818.1985.tb02637.x

Source DB:  PubMed          Journal:  J Microsc        ISSN: 0022-2720            Impact factor:   1.758


  5 in total

1.  Collagen and proteoglycan in a sea urchin ligament with mutable mechanical properties.

Authors:  J A Trotter; T J Koob
Journal:  Cell Tissue Res       Date:  1989-12       Impact factor: 5.249

Review 2.  Proteoglycan-fibrillar collagen interactions.

Authors:  J E Scott
Journal:  Biochem J       Date:  1988-06-01       Impact factor: 3.857

3.  Axial electron density of human scleral collagen. Location of proteoglycans by x-ray diffraction.

Authors:  A J Quantock; K M Meek
Journal:  Biophys J       Date:  1988-07       Impact factor: 4.033

4.  Identification and characterization of glycanated and non-glycanated forms of biglycan and decorin in the human intervertebral disc.

Authors:  B Johnstone; M Markopoulos; P Neame; B Caterson
Journal:  Biochem J       Date:  1993-06-15       Impact factor: 3.857

5.  Decorin core protein (decoron) shape complements collagen fibril surface structure and mediates its binding.

Authors:  Joseph P R O Orgel; Aya Eid; Olga Antipova; Jordi Bella; John E Scott
Journal:  PLoS One       Date:  2009-09-15       Impact factor: 3.240

  5 in total

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