Abstract
Small, hydrophilic molecules, including most important antibiotics in clinical use, cross the Gram-negative outer membrane through the water-filled channels provided by porins. We have determined the X-ray crystal structures of the principal general porins from three species of Enterobacteriaceae, namely Enterobacter aerogenes, Enterobacter cloacae, and Klebsiella pneumoniae, and determined their antibiotic permeabilities as well as those of the orthologues from Escherichia coli. Starting from the structure of the porins and molecules, we propose a physical mechanism underlying transport and condense it in a computationally efficient scoring function. The scoring function shows good agreement with in vitro penetration data and will enable the screening of virtual databases to identify molecules with optimal permeability through porins and help to guide the optimization of antibiotics with poor permeation.
| Original language | English |
|---|---|
| Pages (from-to) | 1487-1498 |
| Number of pages | 12 |
| Journal | ACS Infectious Diseases |
| Volume | 4 |
| Issue number | 10 |
| Early online date | 2 Jul 2018 |
| DOIs | |
| Publication status | Published - 12 Oct 2018 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- bacteria
- antibiotics
- rational design
- porins structure
- transport
- scoring function
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