Water-Insoluble High-Molecular-Weight and Alpha-Crystallins as the Source of the Scheimpflug Light Scattering Pattern in the Rat Lens

1990 ◽  
Vol 22 (1) ◽  
pp. 90-94 ◽  
Author(s):  
J. Bours ◽  
M.H.J. Ahrend ◽  
A. Wegener ◽  
O. Hockwin
Keyword(s):  
Molecular Weight ◽  
Light Scattering ◽  
High Molecular Weight ◽  
Scattering Pattern

scholarly journals The effect of acid mucopolysaccharides and acid mucopolysaccharide–proteins on fibril formation from collagen solutions

1968 ◽  
Vol 109 (4) ◽  
pp. 517-526 ◽  
Author(s):  
M B Mathews ◽  
L. Decker
Keyword(s):  
Molecular Weight ◽  
Light Scattering ◽  
High Molecular Weight ◽  
Chondroitin Sulphate ◽  
Fibril Formation ◽  
Acid Mucopolysaccharide ◽  
Acid Mucopolysaccharides ◽  
Electrostatic Binding ◽  
Fibril Aggregates ◽  
Chondroitin Sulphate A

1. The effects of acid mucopolysaccharides and acid mucopolysaccharide–proteins on the size and rate of formation of fibril aggregates from collagen solutions in pH7·6 buffers were studied by turbidimetric and light-scattering methods. 2. Serum albumin, orosomucoid, methylated cellulose, chondroitin sulphate A and chondroitin sulphate C of molecular weight less than 20000, and hyaluronate of molecular weight less than 40000 did not influence rates of fibril formation. Chondroitin sulphate A, chondroitin sulphate C and hyaluronate of high molecular weight retarded the rate of fibril formation. This effect of high-molecular-weight chondroitin sulphate C decreased with increasing ionic strength. Heparin, though of low molecular weight (13000), was highly effective, as was also heparitin sulphate. The chondroitin sulphate–proteins of very high molecular weight were highly effective, despite the fact that for some preparations the component chondroitin sulphate chains had molecular weights much less than 20000. 3. Agents that had delayed fibril formation were also effective in producing an increase in degree of aggregation of fibrillar collagen, as indicated by dissymmetry changes observed in light-scattering experiments at low collagen concentrations. Methylated cellulose and heparin at 2·5μg./ml. were unusual in decreasing aggregation, but heparin at 0·25μg./ml. increased aggregation. Electron microscopy of gels showed fibrils and fibril aggregates with ‘normal’ collagen spacing and dimensions consistent with the light-scattering results. 4. The rates of electrical transport of agents and of solvent (electro-osmosis) through collagen gels indicated a contribution of molecular entanglement that increased with increase in molecular size of the agents. Electrostatic binding of heparin to collagen was noted. Binding to collagen during fibril formation was also found for heparitin sulphate and a chondroitin sulphate with extra sulphate groups. 5. Electrostatic binding of acid mucopolysaccharide–proteins to collagen may be an important factor in the organization and functioning of connective tissues at all stages of growth and development. Excluded-volume (molecular-entanglement) effects may also be important. These factors operate simultaneously and interact mutually so that precise assessment of their relative importance is difficult.

Sign in / Sign up

Export Citation Format

Share Document