Your browser doesn't support javascript.
loading
Design and Synthesis of PEG-Oligoglycerol Sulfates as Multivalent Inhibitors for the Scavenger Receptor LOX-1.
Kumari, Shalini; Achazi, Katharina; Dey, Pradip; Haag, Rainer; Dernedde, Jens.
Affiliation
  • Kumari S; Institute for Chemistry and Biochemistry, Freie Universität Berlin , Takustr. 3 , 14195 Berlin , Germany.
  • Achazi K; Institute for Chemistry and Biochemistry, Freie Universität Berlin , Takustr. 3 , 14195 Berlin , Germany.
  • Dey P; Institute for Chemistry and Biochemistry, Freie Universität Berlin , Takustr. 3 , 14195 Berlin , Germany.
  • Haag R; Institute for Chemistry and Biochemistry, Freie Universität Berlin , Takustr. 3 , 14195 Berlin , Germany.
  • Dernedde J; Institute of Laboratory Medicine, Clinical Chemistry and Pathobiochemistry, Charité-Universitätsmedizin Berlin , Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Augustenburger Platz 1 , 13353 Berlin , Germany.
Biomacromolecules ; 20(3): 1157-1166, 2019 03 11.
Article in En | MEDLINE | ID: mdl-30642176
Lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1) is a cell surface scavenger receptor. The protein is involved in binding and internalization of oxidized low-density lipoprotein (oxLDL), which leads under pathophysiological circumstances to plaque formation in arteries and initiation of atherosclerosis. A structural feature of LOX-1 relevant to oxLDL binding is the "basic spine" motif consisting of linearly aligned arginine residues stretched over the dimer surface. Inhibition of LOX-1 can be done by blocking these positively charged motifs. Here we report on the design, synthesis, and evaluation of a series of novel LOX-1 inhibitors having different numbers of sulfates and polyethylene glycerol (PEG) spacer. Two molecules, compounds 6b and 6d, showed binding affinity in the low nM range, i.e. 45.8 and 47.4 nM, respectively. The in vitro biological studies reveal that these molecules were also able to block the interaction of LOX-1 with its cognate ligands oxLDL, aged RBC, and bacteria.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polyethylene Glycols / Sulfates / Drug Design / Scavenger Receptors, Class E / Glycerol Limits: Humans Language: En Journal: Biomacromolecules Journal subject: BIOLOGIA MOLECULAR Year: 2019 Document type: Article Affiliation country: Germany Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polyethylene Glycols / Sulfates / Drug Design / Scavenger Receptors, Class E / Glycerol Limits: Humans Language: En Journal: Biomacromolecules Journal subject: BIOLOGIA MOLECULAR Year: 2019 Document type: Article Affiliation country: Germany Country of publication: United States