Plasminogen (Pg), a pro-protease implicated in neuronal excitotoxicity, has recently been identified as binding to prion protein (PrP) from several species. Although the precise effect of the binding of PrP to plasminogen in the course of prion-caused diseases has not yet been demonstrated, the implications of this important finding for diagnostic applications are straightforward. In this paper we have investigated the possible modes of interaction of PrP with plasminogen, by means of molecular modelling and computational simulation techniques. To this goal, we first exploited the information available for the mK2(Pg)/VEK-30 complex in order to identify the PrP residues which satisfy the specific electronic and geometric requirements needed to interact with the kringle lysine binding site, we compared the relevant mK2(Pg)/VEK-30 and mK2(Pg)/PrP interactions obtained from the simulated protein-protein complexes and we assessed the docking hypothesis utilized for the mK2(Pg)/PrP complex by simulating the interaction of PrP with the multi-kringle angiostatin, a more realistic model of the physiological target. The results obtained will be instrumental for planning experiments tailored to clarify the role of the plasminogen activator system in prion-related diseases and, eventually, for mimicking dominant binding determinants through structure-based drug design.

Seeking for binding determinants of the prion protein to human plasminogen / Menziani, Maria Cristina; DE BENEDETTI, Pier Giuseppe; E., Langella; V., Barone. - In: MOLECULAR PHYSICS. - ISSN 0026-8976. - STAMPA. - 101:(2003), pp. 2763-2773.

Seeking for binding determinants of the prion protein to human plasminogen

MENZIANI, Maria Cristina;DE BENEDETTI, Pier Giuseppe;
2003-01-01

Abstract

Plasminogen (Pg), a pro-protease implicated in neuronal excitotoxicity, has recently been identified as binding to prion protein (PrP) from several species. Although the precise effect of the binding of PrP to plasminogen in the course of prion-caused diseases has not yet been demonstrated, the implications of this important finding for diagnostic applications are straightforward. In this paper we have investigated the possible modes of interaction of PrP with plasminogen, by means of molecular modelling and computational simulation techniques. To this goal, we first exploited the information available for the mK2(Pg)/VEK-30 complex in order to identify the PrP residues which satisfy the specific electronic and geometric requirements needed to interact with the kringle lysine binding site, we compared the relevant mK2(Pg)/VEK-30 and mK2(Pg)/PrP interactions obtained from the simulated protein-protein complexes and we assessed the docking hypothesis utilized for the mK2(Pg)/PrP complex by simulating the interaction of PrP with the multi-kringle angiostatin, a more realistic model of the physiological target. The results obtained will be instrumental for planning experiments tailored to clarify the role of the plasminogen activator system in prion-related diseases and, eventually, for mimicking dominant binding determinants through structure-based drug design.
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Seeking for binding determinants of the prion protein to human plasminogen / Menziani, Maria Cristina; DE BENEDETTI, Pier Giuseppe; E., Langella; V., Barone. - In: MOLECULAR PHYSICS. - ISSN 0026-8976. - STAMPA. - 101:(2003), pp. 2763-2773.
Menziani, Maria Cristina; DE BENEDETTI, Pier Giuseppe; E., Langella; V., Barone
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/308045
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