TY - JOUR
T1 - Interactions between dendrimers and heparin and their implications for the anti-prion activity of dendrimers
AU - Klajnert, Barbara
AU - Cangiotti, Michela
AU - Calici, Sara
AU - Ionov, Maksim
AU - Majoral, Jean Pierre
AU - Caminade, Anne Marie
AU - Cladera, Josep
AU - Bryszewska, Maria
AU - Ottaviani, Maria Francesca
PY - 2009/12/1
Y1 - 2009/12/1
N2 - Heparin is involved in the pathogenesis of prion diseases, affecting the process of fibril formation. It has been shown that whether it accelerates or inhibits fibrilogenesis depends on its concentration: prion peptide PrP 185-208 aggregates in the presence of 0.04 mg ml-1 heparin, but concentrations ten times lower or higher cause no aggregation. Polyamidoamine, polypropyleneimine and phosphorus dendrimers that previously exhibited anti-prion activity have been shown to interact with heparin. The interactions between cationic dendrimers and anionic heparin are mainly electrostatic. The present study shows that these interactions are indirectly responsible for the inhibition or enhancement of fibril formation by dendrimers. © 2009 The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.
AB - Heparin is involved in the pathogenesis of prion diseases, affecting the process of fibril formation. It has been shown that whether it accelerates or inhibits fibrilogenesis depends on its concentration: prion peptide PrP 185-208 aggregates in the presence of 0.04 mg ml-1 heparin, but concentrations ten times lower or higher cause no aggregation. Polyamidoamine, polypropyleneimine and phosphorus dendrimers that previously exhibited anti-prion activity have been shown to interact with heparin. The interactions between cationic dendrimers and anionic heparin are mainly electrostatic. The present study shows that these interactions are indirectly responsible for the inhibition or enhancement of fibril formation by dendrimers. © 2009 The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.
U2 - 10.1039/b820632p
DO - 10.1039/b820632p
M3 - Article
VL - 33
SP - 1087
EP - 1093
IS - 5
ER -