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- W3174261968 abstract "The connexin family is a diverse group of highly regulated wide-pore channels permeable to biological signaling molecules. Despite the critical roles of connexins in mediating selective molecular signaling in health and disease, the basis of molecular permeation through these pores remains unclear. Here, we report the thermodynamics and kinetics of binding and transport of a second messenger, adenosine-3',5'-cyclophosphate (cAMP), through a connexin26 hemichannel (Cx26). First, inward and outward fluxes of cAMP molecules solvated in KCl solution were obtained from 4 μs of ± 200 mV simulations. These fluxes data yielded a single-channel permeability of cAMP and cAMP/K+ permeability ratio consistent with experimentally measured values. The results from voltage simulations were then compared with the potential of mean force (PMF) and the mean first passage times (MFPTs) of a single cAMP without voltage, obtained from a total of 16.5 μs of Voronoi-tessellated Markovian milestoning simulations. Both the voltage simulations and the milestoning simulations revealed two cAMP-binding sites, for which the binding constants KD and dissociation rates koff were computed from PMF and MFPTs. The protein dipole inside the pore produces an asymmetric PMF, reflected in unequal cAMP MFPTs in each direction once within the pore. The free energy profiles under opposite voltages were derived from the milestoning PMF and revealed the interplay between voltage and channel polarity on the total free energy. In addition, we show how these factors influence the cAMP dipole vector during permeation, and how cAMP affects the local and nonlocal pore diameter in a position-dependent manner." @default.
- W3174261968 created "2021-07-05" @default.
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- W3174261968 date "2021-08-01" @default.
- W3174261968 modified "2023-10-17" @default.
- W3174261968 title "Free energy and kinetics of cAMP permeation through connexin26 via applied voltage and milestoning" @default.
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- W3174261968 doi "https://doi.org/10.1016/j.bpj.2021.06.024" @default.
- W3174261968 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/8391066" @default.
- W3174261968 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/34214529" @default.
- W3174261968 hasPublicationYear "2021" @default.
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