Manipulation of charge distribution in the arginine and glutamate clusters of the OmpG pore alters sugar specificity and ion selectivity.

Autor: Schmitt C; Division of Biochemistry and Applied Protein Center Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, D-91058 Erlangen, Germany; Department Biology, Division of Plant Physiology, Philipps-University Marburg, D-35043 Marburg, Germany. Electronic address: christine.schmitt@fau.de., Bafna JA; Department of Life Sciences and Chemistry, Jacobs University Bremen, D-28719 Bremen, Germany. Electronic address: j.bafna@jacobs-university.de., Schmid B; Division of Biotechnology and Applied Protein Center Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, D-91058 Erlangen, Germany. Electronic address: benedikt.schmid@fau.de., Klingl S; Division of Biotechnology and Applied Protein Center Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, D-91058 Erlangen, Germany. Electronic address: sklingl@biologie.uni-erlangen.de., Baier S; Division of Biochemistry and Applied Protein Center Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, D-91058 Erlangen, Germany., Hemmis B; Department of Biology and Chemistry, University of Osnabrück, D-49069 Osnabrück, Germany., Wagner R; Department of Life Sciences and Chemistry, Jacobs University Bremen, D-28719 Bremen, Germany; Department of Biology and Chemistry, University of Osnabrück, D-49069 Osnabrück, Germany. Electronic address: ri.wagner@jacobs-university.de., Winterhalter M; Department of Life Sciences and Chemistry, Jacobs University Bremen, D-28719 Bremen, Germany. Electronic address: m.winterhalter@jacobs-university.de., Voll LM; Division of Biochemistry and Applied Protein Center Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, D-91058 Erlangen, Germany; Department Biology, Division of Plant Physiology, Philipps-University Marburg, D-35043 Marburg, Germany. Electronic address: lars.voll@biologie.uni-marburg.de.
Jazyk: angličtina
Zdroj: Biochimica et biophysica acta. Biomembranes [Biochim Biophys Acta Biomembr] 2019 Oct 01; Vol. 1861 (10), pp. 183021. Date of Electronic Publication: 2019 Jul 13.
DOI: 10.1016/j.bbamem.2019.07.009
Abstrakt: OmpG is a general diffusion pore in the E. coli outer membrane with a molecular architecture comprising a 14-stranded β-barrel scaffold and unique structural features. In contrast to other non-specific porins, OmpG lacks a central constriction zone and has an exceptionally wide pore diameter of about 13 Å. The equatorial plane of OmpG harbors an annulus of four alternating basic and acidic patches whose function is only poorly characterized. We have investigated the role of charge distribution for ion selectivity and sugar transport with the help of OmpG variants mutated in the annulus. Substituting the glutamate residues of the annulus for histidines or alanines led to a strong reduction in cation selectivity. Replacement of the glutamates in the annulus by histidine residues also disfavored the passage of pentoses and hexoses relative to disaccharides. Our results demonstrate that despite the wide pore diameter, an annulus only consisting of two opposing basic patches confers reduced cation and monosaccharide transport compared to OmpG wild type. Furthermore, randomization of charged residues in the annulus had the potential to abolish pH-dependency of sugar transport. Our results indicate that E 15 , E 31 , R 92 , R 111 and R 211 in the annulus form electrostatic interactions with R 228 , E 229 and D 232 in loop L6 that influence pH-dependency of sugar transport.
(Copyright © 2019. Published by Elsevier B.V.)
Databáze: MEDLINE
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