Mechanosensitive Gold Colloidal Membranes Mediated by Supramolecular Interfacial Self-Assembly

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Coelho, João Paulo and Mayoral, María José and Camacho, Luis and Martín-Romero, María T. and Tardajos Rodríguez, Gloria and López-Montero, Iván and Sanz García, Eduardo and Ávila Brande, David and Giner-Casares, Juan José and Fernández, Gustavo and Guerrero Martínez, Andrés (2017) Mechanosensitive Gold Colloidal Membranes Mediated by Supramolecular Interfacial Self-Assembly. Journal of the American Chemical Society, 139 (3). pp. 1120-1128. ISSN 0002-7863

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Official URL: https://doi.org/10.1021/jacs.6b09485



Abstract

The ability to respond toward mechanical stimuli is a fundamental property of biological organisms at both the macroscopic and cellular levels, yet it has been considerably less observed in artificial supramolecular and colloidal homologues. An archetypal example in this regard is cellular mechanosensation, a process by which mechanical forces applied on the cell membrane are converted into biochemical or electrical signals through nanometer-scale changes in molecular conformations. In this article, we report an artificial gold nanoparticle (Au NP)−discrete π-conjugated molecule hybrid system that mimics the mechanical behavior of biological membranes and is able to self-assemble into colloidal gold nanoclusters or membranes in a controlled and reversible fashion by changing the concentration or the mechanical force (pressure) applied. This has been achieved by rational design of a small π-conjugated thiolated molecule that controls, to a great extent, the hierarchy levels involved in Au NP clustering by enabling reversible, cooperative non-covalent (π−π, solvophobic, and hydrogen bonding) interactions. In addition, the Au NP membranes have the ability to entrap and release aromatic guest molecules reversibly (Kb = 5.0 × 105 M−1 ) for several cycles when subjected to compression−expansion experiments, in close analogy to the behavior of cellular mechanosensitive channels. Not only does our hybrid system represent the first example of a reversible colloidal membrane, but it also can be controlled by a dynamic mechanical stimulus using a new supramolecular surface-pressure-controlled strategy. This approach holds great potential for the development of multiple colloidal assemblies within different research fields.


Item Type:Article
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The research leading to these results has received funding from the European Research Council under the European Union's Seventh Framework Programme (ERC grant agreement n° 338133)

Subjects:Sciences > Chemistry > Materials
Sciences > Chemistry > Chemistry, Physical and theoretical
ID Code:60111
Deposited On:23 Apr 2020 08:44
Last Modified:23 Apr 2020 08:44

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