Literature DB >> 15299949

Channels in the gramicidin S-with-urea structure and their possible relation to transmembrane ion transport.

G N Tishchenko1, V I Andrianov, B K Vainstein, M M Woolfson, E Dodson.   

Abstract

The structure of membrane-active antibiotic cyclodecapeptide gramicidin S in the crystals of its complex with urea, C(60)H(92)N(12)0(10).0.(5)[(NH(2))(2)CO].7.94H(2)0, has been investigated with three-dimensional X-ray data by the automatic sequential approximation method. The crystals are trigonal, space group P3(1)21, a = 25.80(3), c= 21.49 (2) A, M(r) = 7968, calculated density = 1.088 mg m(-3), Z = 1. Conventional R factor: R1 = 0.0943, wR2 = 0.2478 [I> 2sigma(I)]. The molecule possesses an antiparallel twisted beta-structure, with turns involving the Phe-Pro peptides. The Orn side chains extend on one side of the sheet, while the non-polar Val and Leu side chains are located on the other face. One of the Orn residues (namely Orn2) is linked by an intermolecular hydrogen bond to the O atom of Phe4 residue, the other is free. The side chains of the Phe residues have trans orientation (chi(1) approximately 180 degrees ) and those of the Val, Orn, Leu residues, except those of Orn2, have the preferential gauche orientation with the chi(1) angle close to 60. Two side chains show statistical disorder and conformation of the Pro residues is C(s)-C(beta)-exo. There is half a urea molecule and also 7.94 water molecules distributed on 13 positions for each antibiotic molecule. A partially occupied and poorly ordered alcohol molecule had been identified. The gramicidin S molecules are arranged around the 3(1) axis in the form of a left-handed double spiral forming suggestive channels. The outer hydrophobic surface of the spiral is made of uncharged side radicals while the inside surface consists of the main-chain atoms, mainly O and N, and of ornithine side chains with N atoms at the ends. By changing the Orn side-chain conformation, the inner diameter of the channels may change from 3.4 to 6.3 A. Thus, ions and particles of rather large size may pass through the channel. The possibility of the creation of the gramicidin S channels in mitochondrial membranes has been noted by some biochemists. The channel complexes are close-packed in a hexagonal arrangement in the crystal. The CI(-) ions, present in abundance in the mother solution, are not found ordered in the crystals, which may indicate the absence of the charges in the terminal N atoms of the Orn residues.

Entities:  

Year:  1997        PMID: 15299949     DOI: 10.1107/S0907444995000916

Source DB:  PubMed          Journal:  Acta Crystallogr D Biol Crystallogr        ISSN: 0907-4449


  9 in total

1.  Interaction of gramicidin S and its aromatic amino-acid analog with phospholipid membranes.

Authors:  Masoud Jelokhani-Niaraki; Robert S Hodges; Joseph E Meissner; Una E Hassenstein; Laura Wheaton
Journal:  Biophys J       Date:  2008-07-11       Impact factor: 4.033

2.  Fermentation and Cost-Effective 13C/15N Labeling of the Nonribosomal Peptide Gramicidin S for Nuclear Magnetic Resonance Structure Analysis.

Authors:  Marina Berditsch; Sergii Afonin; Anna Steineker; Nataliia Orel; Igor Jakovkin; Christian Weber; Anne S Ulrich
Journal:  Appl Environ Microbiol       Date:  2015-03-20       Impact factor: 4.792

3.  On resin amino acid side chain attachment strategy for the head to tail synthesis of new glutamine containing gramicidin-S analogs and their antimicrobial activity.

Authors:  Safa Derbal; Mary Hensler; Weiqin Fang; Victor Nizet; Kamel Ghedira; Adel Nefzi
Journal:  Bioorg Med Chem Lett       Date:  2010-08-08       Impact factor: 2.823

4.  Sequence inversion and phenylalanine surrogates at the beta-turn enhance the antibiotic activity of gramicidin S.

Authors:  Concepción Solanas; Beatriz G de la Torre; María Fernández-Reyes; Clara M Santiveri; M Angeles Jiménez; Luis Rivas; Ana I Jiménez; David Andreu; Carlos Cativiela
Journal:  J Med Chem       Date:  2010-05-27       Impact factor: 7.446

5.  Ion mobility-mass spectrometry applied to cyclic peptide analysis: conformational preferences of gramicidin S and linear analogs in the gas phase.

Authors:  Brandon T Ruotolo; Colby C Tate; David H Russell
Journal:  J Am Soc Mass Spectrom       Date:  2004-06       Impact factor: 3.109

6.  Macrocyclic design strategies for small, stable parallel beta-sheet scaffolds.

Authors:  Felix Freire; Samuel H Gellman
Journal:  J Am Chem Soc       Date:  2009-06-17       Impact factor: 15.419

7.  Therapeutic index of gramicidin S is strongly modulated by D-phenylalanine analogues at the beta-turn.

Authors:  Concepción Solanas; Beatriz G de la Torre; María Fernández-Reyes; Clara M Santiveri; M Angeles Jiménez; Luis Rivas; Ana I Jiménez; David Andreu; Carlos Cativiela
Journal:  J Med Chem       Date:  2009-02-12       Impact factor: 7.446

8.  The high resolution structure of tyrocidine A reveals an amphipathic dimer.

Authors:  Patrick J Loll; Elizabeth C Upton; Virginie Nahoum; Nicoleta J Economou; Simon Cocklin
Journal:  Biochim Biophys Acta       Date:  2014-02-11

9.  Design, crystal structure and atomic force microscopy study of thioether ligated d,l-cyclic antimicrobial peptides against multidrug resistant Pseudomonas aeruginosa.

Authors:  Runze He; Ivan Di Bonaventura; Ricardo Visini; Bee-Ha Gan; Yongchun Fu; Daniel Probst; Alexandre Lüscher; Thilo Köhler; Christian van Delden; Achim Stocker; Wenjing Hong; Tamis Darbre; Jean-Louis Reymond
Journal:  Chem Sci       Date:  2017-09-04       Impact factor: 9.825

  9 in total

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