4.7 Article

Improved Parameterization of Phosphatidylinositide Lipid Headgroups for the Martini 3 Coarse-Grain Force Field

Journal

JOURNAL OF CHEMICAL THEORY AND COMPUTATION
Volume 18, Issue 1, Pages 357-373

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jctc.1c00615

Keywords

-

Funding

  1. Medical Biochemistry and Biophysics Doctoral Program (M2B-PhD) [PD/BD/137492/2018]
  2. Fundacao para a Ciencia e a Tecnologia-Ministerio da Ciencia, Tecnologia e Ensino Superior (FCT-MCTES, Portugal) [PD/BD/137492/2018]
  3. FCT-MCTES [CEECIND/04124/2017]
  4. FCT [UIDB/04612/2020, UIDP/04612/2020]
  5. Fundação para a Ciência e a Tecnologia [PD/BD/137492/2018] Funding Source: FCT

Ask authors/readers for more resources

Phosphoinositides are crucial for membrane regulatory events and play a key role in molecular dynamics simulation studies, particularly using coarse-grain models. The recently published Martini 3 version refines biomolecular interactions and provides specific parameterization for phosphoinositides. These models improve conformational dynamics and stability in lipid membrane simulations, reproducing experimentally known behaviors.
Phosphoinositides are a family of membrane phospholipids that play crucial roles in membrane regulatory events. As such, these lipids are often a key part of molecular dynamics simulation studies of biological membranes, in particular of those employing coarse-grain models because of the potential long times and sizes of the involved membrane processes. Version 3 of the widely used Martini coarse-grain force field has been recently published, greatly refining many aspects of biomolecular interactions. In order to properly use it for lipid membrane simulations with phosphoinositides, we put forth the Martini 3-specific parameterization of inositol, phosphatidylinositol, and seven physiologically relevant phosphorylated derivatives of phosphatidylinositol. Compared to parameterizations for earlier Martini versions, focus was put on a more accurate reproduction of the behavior seen in both atomistic simulations and experimental studies, including the signaling-relevant phosphoinositide interaction with divalent cations. The models that we develop improve upon the conformational dynamics of phosphoinositides in the Martini force field and provide stable topologies at typical Martini time steps. They are able to reproduce experimentally known protein-binding poses as well as phosphoinositide aggregation tendencies. The latter was tested both in the presence and absence of calcium and included correct behavior of PI(4,5)P-2 calcium-induced clusters, which can be of relevance for regulation.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available