Jacopo D ' Ascenzi’s research while affiliated with University of Pisa and other places

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Publications (1)


Figure 6: Geometrical analysis of the L1-Lut/Chl a612 pair in LHCSR1. A. L1-Lut in a reference frame centered in Chl a612. The axes are shown in red (x) and green (y). A representative structure from CL2 is shown alongside a representative structure from CL5. The orange arrow underlines the sliding towards the stroma of L1-Lut in CL2. B. Scatter plot of the center of mass displacement of the L1-Lut isoprenic chain with respect to a reference system fixed onto the Mg 2+ ion of Chl a612. The mean of each cluster is indicated with a star. The covariance ellipse enclosing 40% of the data is also reported.
How the pH controls photoprotection in the light-harvesting complex of mosses
  • Preprint
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January 2023

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Jacopo D ' Ascenzi

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In response to varying light conditions, light-harvesting complexes (LHCs) switch from a light-harvesting to a quenched state to protect the photosynthetic organism from excessive light irradiation, in a strategy known as nonphotochemical quenching (NPQ). NPQ is activated by an acidification of the thylakoid lumen which is sensed directly or indirectly by the LHC, resulting in a conformational change of the complex that leads to the quenched state. The conformational changes responsible for NPQ activation and their connection to specific quenching mechanisms are still unknown. Here, we investigate the pH-triggered conformational changes in the light-harvesting complex stress-related (LHCSR) of mosses. By combining constant-pH molecular dynamics and enhanced sampling techniques, we find that the pH sensitivity of the complex is driven by the coupled protonation of three residues modulating the conformation of the short amphipathic helix placed at lumen side of the embedding membrane. Combining these results with quantum mechanics/molecular mechanics calculations, we show that the quenching mechanism sensitive to the pH goes through a charge-transfer between a carotenoid and an excited chlorophyll which is controlled by the protein conformation.

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