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. 2020 Sep;18(9):2422-2424.
doi: 10.1111/jth.14898. Epub 2020 Aug 27.

Heparin - An old drug with multiple potential targets in Covid-19 therapy

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Heparin - An old drug with multiple potential targets in Covid-19 therapy

Ulf Lindahl et al. J Thromb Haemost. 2020 Sep.
No abstract available

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Figures

Figure 1
Figure 1
The structural/functional relationship between heparin and heparan sulfate provides the following. (A) Conjectured heparin chain composed of alternating units of hexuronic acid (D‐glucuronic acid, GlcA, or L‐iduronic acid, IdoA) and D‐glucosamine (GlcN); sulfate groups are indicated by yellow circles. The AT‐binding pentasaccharide sequence carries a unique sulfate group at carbon 3 of the internal GlcN residue; this 3‐O‐sulfate group is present in HA‐ but not in LA‐heparin. (B) HS structure, composed of the same building blocks as heparin, but with more sparse distribution of IdoA and sulfate residues. These components are typically accumulated in more densely sulfated domains that vary in structure depending on cellular origin. The sulfated domains provide sites for interactions of varying specificity with a multitude of proteins. (C) Schematic illustration of two proteins with distinct requirements for binding structures on HS chains, yet both interacting with heparin. Rather than nonspecific, such interaction may depend on “hidden specificity,” the selective HS epitopes being expressed also in the heavily sulfated heparin chain, albeit masked by redundant sulfate groups.

Comment in

References

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