Abstract
It was shown that sulfated pectin derivatives bind human serum low-density lipoproteins (LDLs) in vitro to a greater extent than native pectins. At the same time, the number of sulfate groups and the molecular weight of sulfated derivatives were crucial factors. The sulfated pectin derivatives with molecular weights more than 200 kDa containing 45 wt % sulfate groups had the greatest ability to bind LDLs, while the sulfated derivatives with molecular weights lower than 50 kDa containing 5% sulfate groups exhibited the lowest activity.
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Abbreviations
- BC:
-
Bergenia crassifolia pectin
- BCS1, BCS2, and BCS3:
-
sulfated derivatives of BC
- LM:
-
Lemna minor pectin
- LMS1, LMS2, and LMS3:
-
sulfated derivatives of LM
- PN:
-
Potamogeton natans pectin
- PNS1, PNS2, and PNS3:
-
sulfated derivatives of PN
- HDL:
-
high-density lipoprotein
- LDL:
-
low-density lipoprotein
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Original Russian Text © F.V. Vityazev, N.M. Paderin, V.V. Golovchenko, 2012, published in Bioorganicheskaya Khimiya, 2012, Vol. 38, No. 3, pp. 365–369.
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Vityazev, F.V., Paderin, N.M. & Golovchenko, V.V. In vitro binding of human serum low-density lipoproteins by sulfated pectin derivatives. Russ J Bioorg Chem 38, 319–323 (2012). https://doi.org/10.1134/S1068162012030156
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DOI: https://doi.org/10.1134/S1068162012030156