Crystal structure and surface characteristics of the human dermcidin channel. (A) X-ray structure of the hexameric DCD channel shown in cartoon representation from the side and top (Middle and Right), and as surface representation (Left). The different orientations of the individual peptides relative to the membrane normal are marked in orange and dark blue, and termini are marked (NT, N terminus; CT, C terminus). Arrows combined with tilt angle and axes give the relative orientation. Residues involved in Zn binding are shown in stick representation and Zn ions are marked in gray. The symmetry axis of the channel is marked with C2 (for the side view) and C3 (for the top view). Two interfaces of different surface area are formed after trimerization and named IF1 and IF2. (B) Close-up into the Zn-binding site S1. Four residues (Glu5 and Asp11 from one peptide and Asp41 and His38 from the second) form each Zn-binding site. The distance between the Zn ions is marked by arrows. (C) Electrostatic surface representation of the channel with two monomers marked in ribbon representation. The channel comprises five alternating patches of elongated negative (red) and ring-like positive (blue) charge. (D) Side view of DCD (hydrophobic residues in magenta). (E) Ribbon model of DCD. The pore diameter is represented by spheres. The lateral entry points are marked with circles. (F) Hydrophilic residues on the trimeric interface (negatively charged residues in red, positively charged residues in blue, polar residues in green). Nonpolar residues are shown in white. (G) The hydrophilic channel interior. For clarity, the front dimer is omitted; colors as in F. (H) Channel radius along the pore axis. Copyright © PNAS, doi:10.1073/pnas.1214739110 Frogs skin gives researchers the hop on bacteria (Phys.org) —While the natural world is replete with compounds that form the basis of many disease-fighting pharmaceuticals, it is also the case that humans and other mammals produce their own host-defense peptide-derived broad-spectrum antibiotics to combat bacterial and fungal infections. By attacking microbial cell membranes, these peptides prevent bacteria from developing rapid antibiotic resistance. While over 1,700 of these peptides are known, the structural and mechanical aspects of their functional activity have remained an unanswered question. Recently, however, scientists at Max Planck Institute for Biophysical Chemistry, Max Planck Institute for Developmental Biology, The University of Edinburgh, and other instiutions1 determined the X-ray crystal structure as well as solid-state nuclear magnetic resonance (NMR) spectroscopy, electrophysiology, and molecular dynamic (MD) simulations of human dermcidin (DCD), revealing its mechanism at atomic scale. The researchers conclude that their results may lead to the peptide structure-based design of second-generation antibiotics. PausePlay% buffered00:0000:00UnmuteMuteDisable captionsEnable captionsSettingsCaptionsDisabledQuality0SpeedNormalCaptionsGo back to previous menuQualityGo back to previous menuSpeedGo back to previous menu0.5×0.75×Normal1.25×1.5×1.75×2×Exit fullscreenEnter fullscreen , Nature Prof. Kornelius Zeth spoke with Phys.org about the challenges that he, Dr. Ulrich Zachariae, Dr. Chen Song, Dr. Bert de Groot, and his other colleagues encountered in conducted their research. “For crystallography it was very difficult to find a proper peptide source. In fact, we had to use five different peptides from different companies until we found a company, Peptide 2.0 Inc., which produced the peptide in the correct way,” Zeth recalls. “However, I can’t say they’ve modified their process – and luck also a factor, as are and several parameters which are influential aside from the peptide, such as who conducts the robotic screening, local climate and so on.”Moreover, the simulations that revealed the antibiotic mechanism of human dermcidin had their own complications. “Simulations require time and experience in order to capture the correct lipidic environment,” Zeth adds. “Also, the choice of the proper MD method was critical to tracing the mechanism by which ions passed through the channel.” The simulations went on for many months, he illustrates, depending on the system studied, to get a complete picture of the membrane channels. More specifically, Song notes that the production simulations took more than a year – roughly 650 days – in real time using 48 CPUs.”Several consistency checks were carried out to ensure the validity of the MD simulations,” de Groot points out. “First, the simulation parameters and setup were carefully selected to mimic the bacterial conditions as closely as possible. Second, to ensure convergence the simulations were carried out multiple times, from different starting conditions. Third, the conductance derived from the electrophysiology simulations were directly compared to measured values, showing quantitative agreement.”Another challenge, Zeth says, was conducting electrophysiology experiments in which the scientists characterized the activity of dermcidin in membranes under various conditions. “Methods applied to solve this problem are typically based on recent developments in electrophysiology. One general problem of DCD is that the peptide is very soluble in water and does not easily enter artificial membranes.” in fact, this finding has also caused NMR problems when trying to verify the tilting of the channel in membranes as predicted by MD simulations. These studies were hampered by the small portion of the peptide that was observable in an integral membrane conformation. More information: Crystal structure and functional mechanism of a human antimicrobial membrane channel, PNAS March 19, 2013 vol. 110 no. 12 4586-4591, doi:10.1073/pnas.1214739110Related: 1Georg August University – Göttingen, University of Strasbourg, Centre National de la Recherche Scientifique, Freiburg University, University of Basque Country, Spanish Science Research Council 2Editor’s Summary: Trigger for psoriasis, Nature 4 October 2007 Discussing how their findings articulate the comprehensive mechanism for the membrane-disruptive action of this mammalian host-defense peptide at atomistic level, Zeth notes that their findings are based on the combination of several techniques. “Starting from the crystal structure,” he explains, “we modeled the ion flux, later deciding to verify the theoretical calculations and values by experimental data. We’ve also tried to model the tilting behavior seen in MD simulation by solid state NMR techniques, but this approach failed. Nevertheless, the overall picture, while incomplete, leads to many follow-up experiments and stimulates the AMP community regarding the development of new mechanistic views.” As for the conductance calculated by MD, however, researchers we were able to reproduce these values using planar lipid membrane techniques in an error range of only 20%. While their paper states that their results may form a foundation for the structure-based design of peptide antibiotics, Zeth says that this is rather difficult to judge. “In fact, he says, the German company BRAIN is trying to introduce DCD into pharmaceutical studies. However, if you look closer into the general applications of peptides as AMPs, it’s rather frustrating. To my knowledge,” Zeth acknowledges, “there are no AMP peptides sold as pharmaceuticals at the moment, although the general market of peptides – against cancer and other diseases – is still growing. The problem is the size and stability of the peptides if given orally or into the bloodstream as proteases, but. DCD is active on skin – so might be easier if it was to be introduced into creams.”Zeth then described medical properties and potential of host-defense antimicrobial peptides for comparison with traditional small-molecule antibiotics.Specificity: Rather unspecific. Gram-positives and negatives are concerned while with traditional antibiotics either Gram+/Gram- are treated.Efficacy: likely to be more efficient due to inherent molecular antibacterial propertiesSafety: Not yet determined but as these molecules come from humans they should not be toxicPost-xenotransplantation immune response: Currently unknown. The problem with antimicrobial peptides is protease-based instability in the bloodstream and stomach.Autoimmune diseases: Some peptides, such including LL-37, have severe implications in autoimmunity. In fact, the overproduction of these peptides generates a number of skin diseases, such as psoriasis. More specifically, in the case of psoriasis it seems that LL-37 overproduction can cause autoimmune diseases,2 the unresolved issue being whether the peptides are produced inside or outside the cell.In terms of next steps in their research, Zeth mentions studies of mutations in the membrane-exposed side of the channel; changing properties, such as conductivity or membrane integration, inside the membrane to; peptide translocation via membranes; and mentions post-xenotransplantation immune response as “an idea for future applications.”Zeth notes that other areas of research might benefit from their research. “Generally our study will influence the current view of peptide channels in membranes – an important field, in particular for researchers trying to enhance this domain of knowledge to improve current peptide drugs. Also, our channel study benefits MD for further use in a variety of studies on mutations and different approaches to better characterize the channel. The channel is thereby a tool,” Zeth concludes, “for testing methods and answer questions which were, so far, difficult to answer due to missing structural models.” Journal information: Proceedings of the National Academy of Sciences Citation: Antibiotics 2.0: The atomic structure and mechanism of mammalian host-defense peptides (2013, April 30) retrieved 18 August 2019 from https://phys.org/news/2013-04-antibiotics-atomic-mechanism-mammalian-host-defense.html Play Multiion permeation mechanism across DCD driven by transmembrane electric fields present across bacterial membranes. Ions enter sideways into the pore across the lateral openings that occur at the trimeric interfaces. Anion transfer across the inner pore usually involves single ion “hopping” steps. Near the channel exit, anions accumulate to form a cluster of three to four ions. Ions exiting the channel are often observed to be translocated by multiion “knockon” effects, by which anions are transferred to the bulk solution. Copyright © PNAS, doi:10.1073/pnas.1214739110 “Peptide solubility or membrane affinity can be influenced by several parameters, such as mutations or changing membrane systems,” Zeth continues. “For NMR we’ve seen essentially all of the peptide associated with the membrane in a horizontal manner. However, we were more interested in the peptide complex inserted in the membrane, but that only occurred ten percent or less of the time.” Zeth outlines the key insights and discoveries that helped the team address these challenges. “One important factor was that this was the first structure of an anti-microbial peptide in a channel conformation,” he explains. “Another was that this peptide activity seems to be zinc-dependent – although it is not really clear what activity zinc actually causes. Also,” Zeth adds, “our model, based on the molecular dynamics of ion flow through the channel, is new and unexpected, in that lateral pore openings seem to play a more important role than do terminals.”Zeth points out that their study solved the crystal structure of an AMP (antimicrobial peptide) channel for the first time in a putative channel conformation. “This result allowed a number of follow-up experiments, in particular MD simulations without assembling a rather artificial membrane pore,” he explains. “In my opinion, our AMP structure is the first to be assembled on the basis of direct X-ray data. All other AMPs used for MD are assembled based on indirect data, and while these assemblies may be correct, their structural information cannot be compared to the quality of X-ray data. This allowed us to use a system that reflects the closest membrane-bound state.” © 2013 Phys.org. All rights reserved. Explore further Model system used in the MD simulations. (A) The initial simulation system, which contains the X-ray structure of DCD (orange and deep blue cartoon helices), the POPE/POPG (3:1) lipids bilayer (gray sticks), water box (light blue surface), Na+ (blue spheres), and Cl− (red spheres) ions. (B) The MD conformation after 100-ns simulation, which was then duplicated in the membrane normal direction to form the double-patch simulation system for the computational electrophysiology simulations (C). Copyright © PNAS, doi:10.1073/pnas.1214739110 This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.