Selected article for: "active compound and inhibitory mechanism"

Author: Zhang, Huitu; Sang, Jingcheng; Li, Li; Jiang, Luying; Lu, Fuping; He, Shan; Cui, Wei; Zhang, Xiaoqing; Liu, Fufeng
Title: Molecular basis for the inhibitory effects of 5-hydroxycyclopenicillone on the conformational transition of Aβ40 monomer.
  • Cord-id: 67vlxxw5
  • Document date: 2020_7_29
  • ID: 67vlxxw5
    Snippet: Previous studies have indicated that 5-hydroxycyclopenicillone (HCP), an active compound derived from marine sponge, could inhibit oligomerization of amyloid β-protein (Aβ). However, the molecular basis for the interaction between HCP and Aβ remains unclear. Herein, all-atom molecular dynamics (MD) simulations were used to explore the conformational conversion of an Aβ40 monomer at different concentrations (0-40 mM) of HCP at the atomic level. It is confirmed that the conformational transiti
    Document: Previous studies have indicated that 5-hydroxycyclopenicillone (HCP), an active compound derived from marine sponge, could inhibit oligomerization of amyloid β-protein (Aβ). However, the molecular basis for the interaction between HCP and Aβ remains unclear. Herein, all-atom molecular dynamics (MD) simulations were used to explore the conformational conversion of an Aβ40 monomer at different concentrations (0-40 mM) of HCP at the atomic level. It is confirmed that the conformational transition of the Aβ40 monomer is prevented by HCP in a concentration-dependent manner in silico. In 40 mM HCP solution, the initial α-helix-rich conformation of Aβ40 monomer is kept under the action of HCP. The intra-peptide hydrophobic collapse and D23-K28 salt bridge are prevented by HCP. Moreover, it is indicated that the non-polar binding energy dominates the binding between HCP and Aβ40 monomer as evaluated by molecular mechanics Poisson-Boltzmann surface area method. And, the residues of F4, Y10, V12, L17 and L34 in Aβ40 might contribute to the binding energy in HCP-Aβ40 complex. All these results elucidate the molecular mechanism underlying the inhibitory effects of HCP against the conformational transformation of Aβ40, providing a support that HCP may be developed as a potential anti-Aβ compound for the treatment of Aβ-related diseases. Communicated by Ramaswamy H. Sarma.

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