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1hpn

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(New page: 200px<br /><applet load="1hpn" size="450" color="white" frame="true" align="right" spinBox="true" caption="1hpn" /> '''N.M.R. AND MOLECULAR-MODELLING STUDIES OF TH...)
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'''N.M.R. AND MOLECULAR-MODELLING STUDIES OF THE SOLUTION CONFORMATION OF HEPARIN'''<br />
'''N.M.R. AND MOLECULAR-MODELLING STUDIES OF THE SOLUTION CONFORMATION OF HEPARIN'''<br />
==Overview==
==Overview==
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The solution conformations of heparin and de-N-sulphated, re-N-acetylated, heparin have been determined by a combination of n.m.r. spectroscopic and, molecular-modelling techniques. The 1H- and 13C-n.m.r. spectra of these, polysaccharides have been assigned. Observed 1H-1H nuclear Overhauser, enhancements (n.O.e.s) have been simulated using the program NOEMOL, [Forster, Jones and Mulloy (1989) J. Mol. Graph. 7, 196-201] for molecular, models derived from conformational-energy calculations; correlation times, for the simulations were chosen to fit experimentally determined 13C, spin-lattice relaxation times. In order to achieve good agreement between, calculated and observed 1H-1H n.O.e.s it was necessary to assume that the, reorientational motion of the polysaccharide molecules was not isotropic, but was that of a symmetric top. The resulting model of heparin in, solution is similar to that determined in the fibrous state by, X-ray-diffraction techniques [Nieduszynski, Gardner and Atkins (1977) Am., Chem. Soc. Symp. Ser. 48, 73-80].
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The solution conformations of heparin and de-N-sulphated, re-N-acetylated heparin have been determined by a combination of n.m.r. spectroscopic and molecular-modelling techniques. The 1H- and 13C-n.m.r. spectra of these polysaccharides have been assigned. Observed 1H-1H nuclear Overhauser enhancements (n.O.e.s) have been simulated using the program NOEMOL [Forster, Jones and Mulloy (1989) J. Mol. Graph. 7, 196-201] for molecular models derived from conformational-energy calculations; correlation times for the simulations were chosen to fit experimentally determined 13C spin-lattice relaxation times. In order to achieve good agreement between calculated and observed 1H-1H n.O.e.s it was necessary to assume that the reorientational motion of the polysaccharide molecules was not isotropic, but was that of a symmetric top. The resulting model of heparin in solution is similar to that determined in the fibrous state by X-ray-diffraction techniques [Nieduszynski, Gardner and Atkins (1977) Am. Chem. Soc. Symp. Ser. 48, 73-80].
==About this Structure==
==About this Structure==
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1HPN is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1HPN OCA].
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1HPN is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1HPN OCA].
==Reference==
==Reference==
N.m.r. and molecular-modelling studies of the solution conformation of heparin., Mulloy B, Forster MJ, Jones C, Davies DB, Biochem J. 1993 Aug 1;293 ( Pt 3):849-58. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=8352752 8352752]
N.m.r. and molecular-modelling studies of the solution conformation of heparin., Mulloy B, Forster MJ, Jones C, Davies DB, Biochem J. 1993 Aug 1;293 ( Pt 3):849-58. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=8352752 8352752]
[[Category: Protein complex]]
[[Category: Protein complex]]
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[[Category: Forster, M.J.]]
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[[Category: Forster, M J.]]
[[Category: Mulloy, B.]]
[[Category: Mulloy, B.]]
[[Category: glycosaminoglycan]]
[[Category: glycosaminoglycan]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sun Nov 25 02:53:35 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:03:34 2008''

Revision as of 11:03, 21 February 2008


1hpn

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N.M.R. AND MOLECULAR-MODELLING STUDIES OF THE SOLUTION CONFORMATION OF HEPARIN

Overview

The solution conformations of heparin and de-N-sulphated, re-N-acetylated heparin have been determined by a combination of n.m.r. spectroscopic and molecular-modelling techniques. The 1H- and 13C-n.m.r. spectra of these polysaccharides have been assigned. Observed 1H-1H nuclear Overhauser enhancements (n.O.e.s) have been simulated using the program NOEMOL [Forster, Jones and Mulloy (1989) J. Mol. Graph. 7, 196-201] for molecular models derived from conformational-energy calculations; correlation times for the simulations were chosen to fit experimentally determined 13C spin-lattice relaxation times. In order to achieve good agreement between calculated and observed 1H-1H n.O.e.s it was necessary to assume that the reorientational motion of the polysaccharide molecules was not isotropic, but was that of a symmetric top. The resulting model of heparin in solution is similar to that determined in the fibrous state by X-ray-diffraction techniques [Nieduszynski, Gardner and Atkins (1977) Am. Chem. Soc. Symp. Ser. 48, 73-80].

About this Structure

1HPN is a Protein complex structure of sequences from [1]. Full crystallographic information is available from OCA.

Reference

N.m.r. and molecular-modelling studies of the solution conformation of heparin., Mulloy B, Forster MJ, Jones C, Davies DB, Biochem J. 1993 Aug 1;293 ( Pt 3):849-58. PMID:8352752

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