4.6 Article

Evidence for ATP Interaction with Phosphatidylcholine Bilayers

Journal

LANGMUIR
Volume 35, Issue 30, Pages 9944-9953

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.langmuir.9b01240

Keywords

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Funding

  1. UTS Chancellors Postdoctoral Research Fellowship Scheme
  2. Australian Research Council [DP-121003548, DP-150101112, DP170101732]
  3. Lundbeckfonden
  4. PRACE grant [2016153468]

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ATP is a fundamental intracellular molecule and is thought to diffuse freely throughout the cytosol. Evidence obtained from nucleotide-sensing sarcolemmal ion channels and red blood cells, however, suggest that ATP is compartmentalized or buffered, especially beneath the sarcolemma, but no definitive mechanism for restricted diffusion or potential buffering system has been postulated. In this study, we provide evidence from alterations to membrane dipole potential, membrane conductance, changes in enthalpy of phospholipid phase transition, and from free energy calculations that ATP associates with phospholipid bilayers. Furthermore, all-atom molecular dynamics simulations show that ATP can form aggregates in the aqueous phase at high concentrations. ATP interaction with membranes provides a new model to understand the diffusion of ATP through the cell. Coupled with previous reports of diffusion restriction in the subsarcolemmal space, these findings support the existence of compartmentalized or buffered pools of ATP.

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