Back to Search
Start Over
The Solution Structure of Heparan Sulfate Differs from That of Heparin.
- Source :
-
Journal of Biological Chemistry . 7/15/2011, Vol. 286 Issue 28, p24842-24854. 13p. - Publication Year :
- 2011
-
Abstract
- The highly sulfated polysaccharides heparin and heparan sulfate (HS) play key roles in the regulation of physiological and pathophysiological processes. Despite its importance, no molecular structures of free HS have been reported up to now. By combining analytical ultracentrifugation, small angle x-ray scattering, and constrained scattering modeling recently used for heparin, we have analyzed the solution structures for eight purified HS fragments degree of polymerization 6-18 (dp6- dpl8) and dp24, corresponding to the predominantly unsulfated GIcA-GIcNAc domains of heparan sulfate. Unlike heparin, the sedimentation coefficient s20,w of HS dp6 - dp24 showed a small rotor speed dependence, where similar 520,w values of 0.82-1.26 S (absorbance optics) and 1.05-1.34 S (interference optics) were determined. The corresponding x-ray scattering measurements of HS dp6 - dp24 gave radius of gyration (RG) values from 1.03 to 2.82 nm, cross-sectional radius of gyration (RXS) values from 0.31 to 0.65 nm, and maximum lengths (L) from 3.0 to 10.0 nm. These data showed that HS has a longer and more bent structure than heparin. Constrained scattering modeling starting from 5000-8000 conformationally randomized HS structures gave best fit dp6 - dpl6 molecular structures that were longer and more bent than their equivalents in heparin. No fits were obtained for HS dpl8 or dp24, indicating their higher flexibility. We conclude that HS displays an extended bent conformation that is significantly distinct from that for heparin. The difference is attributed to the different predominant monosaccharide sequence and reduced sulfation of HS, indicating that HS may interact differently with proteins compared with heparin. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 00219258
- Volume :
- 286
- Issue :
- 28
- Database :
- Academic Search Index
- Journal :
- Journal of Biological Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 65093412
- Full Text :
- https://doi.org/10.1074/jbc.M111.226027