Dynamic properties of pH-dependent structural organization of the amyloidogenic beta-protein (1-40)

Abstract

The structural organization of the amyloidogenic beta-protein containing 40 amino acid residues (Abeta40) was studied by the high temperature molecular dynamics simulations in the acidic (pH approximately 3) and basic (pH approximately 8) pH regions. The obtained data suggest that the central Ala21-Gly29 segment of Abeta40 can adopt folded and partially unfolded structures. At the basic pH, this segment forms folded structures stabilized by electrostatic interactions and hydrogen bonds. At the acidic pH, it forms partially unfolded structures. Two other segments flanking to the central segment exhibit the propensity to adopt unstable interconverting alpha-helical, 3(10)-helical and turn-like structures. One of these segments is comprised of the Ala30-Val36 residues at both of the considered pHs. The second segment is comprised of the Glu11-Phe20 at the basic pH and of the Glu11-Val24 residues at the acidic pHs. The revealed pH-dependent structuration of the Abeta40 allowed us to suggest a possible scenario for initial Abeta aggregation. According to this scenario, the occurrence of the partially unfolded states of the Ala21-Gly29 segment plays main role in the Abeta oligomerization process.

Figure 1

Dynamics behavior of the radii of gyration (Rg) of Aβ40 during MD simulations performed for (A and B) initial structures at both considered pHs. Notes: Plots of the radii of gyration calculated (in Angstrom) for backbone atoms (Cα, C, N) of Aβ40 at pH 8 and pH 3 are shown in the upper and lower parts of the figure, correspondingly. Colored curves correspond to the A (magenta) and B (blue) initial structures (see Methods).

Figure 2

Percentage (%) of involvement of the amino acid residues within the Aβ40 sequence in forming the secondary structural elements (structural propensity) during the last 10 ns of MD simulations at pH 8: (A and B) present secondary structure sets determined by the analyses of the RSA₈ and RSB₈ structural sets, correspondingly. Notes: The secondary structure elements were depicted by different colors: α-helix (green), 3₁₀-helix (blue), β-turn (yellow) and random coil (red).

Figure 3

The trace of the C_α-atoms of the average Ω-shaped structure formed by the Ala21-Gly29 segment in the stable state at pH 8.

Figure 4

A typical three-dimensional structure formed by the Glu22-Gly29 segment in the stable state at pH 8. Notes: Observed H-bonds between polar groups are shown by dash-lines. CD, CG, OG and NZ note the heavy atoms of the donor-acceptor groups of the interacting residues.

Figure 5

Schematic presentation of the major structural states of the Glu11-Val36 segment of the Aβ40 core domain considered at pH 8 and pH 3. The rectangular blocks along the sequence designate the flexible and fluctuating helix-like structural modes: Glu11-Phe20 (Helix 1′) at pH 8; Glu11-Val24 (Helix 1) at pH 3, and Ala30-Val36 (Helix 2) at both pHs. The Ala21-Gly29 residues at pH 8 form the Ω-shaped structure (comprised of about 84% of the MD generated structures). The Gly25-Gly29 residues at both pHs form a bend-shaped structure.

Figure 6

Helical net layout of the Glu11-Gly37 segment. Notes: The sequence is presented by the net diagram typical for two α-helices, formed by the Glu11-Val24 (Helix 1) and Ala30-Val36 (Helix 2) segments. The residues forming the continuous hydrophobic clusters are marked by dark circles. The residues forming the bend structures (Gly25-Gly29) are marked by the hexagons. The numbers present the positions of the corresponding amino acid residues in the Aβ40 sequence.