Light Harvesting Complex II Resists Non-bilayer Lipid-Induced Polymorphism in Plant Thylakoid Membranes via Lipid Redistribution

The plant thylakoid membrane hosting the light-harvesting complex (LHCII) is the site of oxygenic photosynthesis. Contrary to the earlier consensus of a protein-driven single lamellar phase of the thylakoid, despite containing 40% non-bilayer-forming lipids, recent experiments confirm the polymorphic state of the functional thylakoid. What, then, is the origin of this polymorphism and what factors control it? The current Letter addresses the question using a total of 617.8 μs long coarse-grained simulations of thylakoids with and without LHCII and varying concentrations of non-bilayer lipids using Martini-2.2 and -3.0 at 323 K. The LHCII redistributes the non-bilayer lipids into its annular region, increases the bending modulus and the stalk formation free energy, reduces the nonzero mean curvature propensity, and resists the polymorphism these lipids promote. The thermodynamic trade-off between non-bilayer lipids and LHCII dictates the degree of nanoscopic curvature leading to the polymorphism crucial for non-photochemical quenching under excess light conditions.

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Publication Details

Journal
The Journal of Physical Chemistry Letters
Published
2024-12-19
DOI
https://doi.org/10.1021/acs.jpclett.4c03300
Citations
3
Primary Topic
Photosynthetic Processes and Mechanisms
Type
article
Field-Weighted Citation Impact
0.70

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article

Light Harvesting Complex II Resists Non-bilayer Lipid-Induced Polymorphism in Plant Thylakoid Membranes via Lipid Redistribution

Avinash Garg, Ananya Debnath
3 citations
The Journal of Physical Chemistry Letters
Photosynthetic Processes and Mechanisms
0.70
article

Light Harvesting Complex II Resists Non-bilayer Lipid-Induced Polymorphism in Plant Thylakoid Membranes via Lipid Redistribution

Avinash Garg, Ananya Debnath
article en
3 citations

Abstract

The plant thylakoid membrane hosting the light-harvesting complex (LHCII) is the site of oxygenic photosynthesis. Contrary to the earlier consensus of a protein-driven single lamellar phase of the thylakoid, despite containing 40% non-bilayer-forming lipids, recent experiments confirm the polymorphic state of the functional thylakoid. What, then, is the origin of this polymorphism and what factors control it? The current Letter addresses the question using a total of 617.8 μs long coarse-grained simulations of thylakoids with and without LHCII and varying concentrations of non-bilayer lipids using Martini-2.2 and -3.0 at 323 K. The LHCII redistributes the non-bilayer lipids into its annular region, increases the bending modulus and the stalk formation free energy, reduces the nonzero mean curvature propensity, and resists the polymorphism these lipids promote. The thermodynamic trade-off between non-bilayer lipids and LHCII dictates the degree of nanoscopic curvature leading to the polymorphism crucial for non-photochemical quenching under excess light conditions.

The Journal of Physical Chemistry LettersVol. 16(1)
Indian Institute of Technology Jodhpur (IN)
Science and Engineering Research Board
Zero hunger
Openalex Percentile: Top 28%
Photosynthetic Processes and Mechanisms
0.70
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