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Estimation of Liposome Penetration Barriers of Drug Molecules with All-Atom and Coarse-Grained Models

Artikel i vetenskaplig tidskrift
Författare Samuel Genheden
Leif A Eriksson
Publicerad i Journal of Chemical Theory and Computation
Volym 12
Nummer/häfte 9
Sidor 4651-4661
ISSN 1549-9618
Publiceringsår 2016
Publicerad vid Institutionen för kemi och molekylärbiologi
Sidor 4651-4661
Språk en
Länkar dx.doi.org/10.1021/acs.jctc.6b00557
Ämnesord free-energy calculations, martini force-field, partition-coefficients, 5-aminolevulinic acid, dynamics simulations, biomolecular simulations, photodynamic therapy, delivery, water, validation, Chemistry, Physics
Ämneskategorier Kemi

Sammanfattning

Liposomes are common carriers of drug molecules, providing enhanced delivery and accumulation of hydrophilic agents or larger biomolecules. Molecular simulations, can be used to estimate key features of the drug molecules upon interaction with the liposomes, such as penetration barriers and localization. Herein, we investigate several aspects of the computational estimation of penetration barriers, viz. the potential of Mean force (PMFs) along a vector spanning the membrane. First, we provide an: evaluation of the all-atom (AA) and coarse-grained (CG) parametrization of 5-aminolevulinic acid (5-ALA) and two of its alkyl esters by computing n-octanol/water partition :Coefficients. We find that the CG parametrization of the esters performs significantly better than the CG model of 5-ALA, highlighting the difficulty to coarse-grain small, polar molecules. However; the expected trend in partition coefficients is reproduced also with the CG models. Second, we compare PMFs in a small membrane slab described with either the AA or CG models. Here, we:are able to reproduce the all-atom PMF of 5-ALA with CG. However, for the alkyl esters it is unfortunately not possible to correctly reproduce both the depth and the penetration barrier of the PMF seen in the AA simulations with any of the tested CG models. We argue that it is more important to, choose a CG parametrization that reproduces the depth of the PMF. Third, we compare, using the CG model, PMFs in the membrane slab with PMFs in a large, realistic liposome. We find similar depths but slightly different penetration barriers most likely due to differences in the lipid density along the membrane axis. Finally, we compute PMFs in liposomes with three different lipid compositions. Unfortunately, differences in the PMFs could not be quantified, and it remains to be investigated to, what extent liposome simulations can fully reproduce experimental findings.

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