openQCM – Powered by Novaetech S.r.l
Publications citing the applications of openQCM (by Novaetech S.r.l.) instruments and accessories in scientific research.
The list of scientific papers published on the most important journals showing the usage of openQCM in several scientific fields, such as thin film deposition, chemical sensors, biological research and biosensors.
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Censor, Semion; Martin, Jorge Vega; Silberbush, Ohad; Reddy, Samala Murali Mohan; Zalk, Ran; Friedlander, Lonia; Trabada, Daniel G.; Mendieta, Jesús; Saux, Guillaume Le; Moreno, Jesús Ignacio Mendieta; Zotti, Linda Angela; Mateo, José Ortega; Ashkenasy, Nurit
Long-Range Proton Channels Constructed via Hierarchical Peptide Self-Assembly Journal Article
In: Advanced Materials, vol. n/a, no. n/a, pp. 2409248, 2024.
Abstract | Links | BibTeX | Tags: Dissipation, molecular dynamic simulations, openQCM Q-1, peptides, proton channels, proton transport, QCM-D, Quartz Crystal Microbalance, self-assembly
@article{https://doi.org/10.1002/adma.202409248,
title = {Long-Range Proton Channels Constructed via Hierarchical Peptide Self-Assembly},
author = {Semion Censor and Jorge Vega Martin and Ohad Silberbush and Samala Murali Mohan Reddy and Ran Zalk and Lonia Friedlander and Daniel G. Trabada and Jesús Mendieta and Guillaume Le Saux and Jesús Ignacio Mendieta Moreno and Linda Angela Zotti and José Ortega Mateo and Nurit Ashkenasy},
url = {https://onlinelibrary.wiley.com/doi/abs/10.1002/adma.202409248},
doi = {https://doi.org/10.1002/adma.202409248},
year = {2024},
date = {2024-11-12},
journal = {Advanced Materials},
volume = {n/a},
number = {n/a},
pages = {2409248},
abstract = {Abstract The quest to understand and mimic proton translocation mechanisms in natural channels has driven the development of peptide-based artificial channels facilitating efficient proton transport across nanometric membranes. It is demonstrated here that hierarchical peptide self-assembly can form micrometers-long proton nanochannels. The fourfold symmetrical peptide design leverages intermolecular aromatic interactions to align self-assembled cyclic peptide nanotubes, creating hydrophilic nanochannels between them. Titratable amino acid sidechains are positioned adjacent to each other within the channels, enabling the formation of hydrogen-bonded chains upon hydration, and facilitating efficient proton transport. Moreover, these chains are enriched with protons and water molecules by interacting with immobile counter ions introduced into the channels, increasing proton flow density and rate. This system maintains proton transfer rates closely resembling those in natural protein channels over micrometer distances. The functional behavior of these inherently recyclable and biocompatible systems opens the door for their exploitation in diverse applications in energy storage and conversion, biomedicine, and bioelectronics.},
keywords = {Dissipation, molecular dynamic simulations, openQCM Q-1, peptides, proton channels, proton transport, QCM-D, Quartz Crystal Microbalance, self-assembly},
pubstate = {published},
tppubtype = {article}
}
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