Metal nanoclusters assembled using short peptides as templates exhibit significant potential for development and application in the fields of catalysis and biomedicine, owing to their distinctive electronic structure, favorable optical properties, and biocompatibility. Among them, tripeptides exhibit a simpler structure and greater flexibility, enabling them to readily co-assemble with other functional components to create novel materials with significant application value. They can be assembled with copper ions to synthesize highly efficient luminescent nanoclusters, which can serve as an effective fluorescent probe. Here, we report a method for the synthesis of copper nanoclusters (Cu NCs) using tripeptides as templates, which also act as stabilizers and reducing agents. The synthesis conditions and properties were explored and optimized. Under optimal conditions, the Cu NCs exhibit excellent stability and are strongly fluorescent. The Cu NCs can detect 0.1–1.0 μmol/L of ascorbic acid with a low detection limit of 0.075 μmol/L, demonstrating high sensitivity and offering significant application potential for the trace of ascorbic acid in various substances. It also provides new ideas for the assembly of metal nanoclusters and the construction of fluorescent probe sensing platforms.

Tannic acid contains a high density of catechol groups, which enable strong interactions with metal ions for the formation of adhesive assembly films. The metal-polyphenol structure formed by tannic acid with metal ions has the advantages of green environmental protection and strong adhesion. In this work, a tannic acid-iron film modified electrode was prepared by a one-step self-assembly method in which ferric chloride hexahydrate and tannic acid were used as reactants. Ultraviolet-visible absorption spectroscopy, scanning electron microscopy, X-ray photoelectron spectroscopy, and infrared spectroscopy were used to characterize the structure and morphology of the tannic acid-iron films. Differential pulse voltammetry was used to evaluate the electrochemical sensing performance of the tannic acid-iron film modified electrode towards dopamine. In the range of 450 μM-4 mM, the response current of the modified electrode has a good linear relationship with the dopamine concentration. An anti-interference test of the modified electrode was performed in an electrolyte containing ascorbic acid and uric acid. The electrode has good anti-interference performance. The successful construction of this sensor provides new insights into the research and design of dopamine electrochemical sensors.

Flexible and stretchable strain sensors can be applied for human health monitoring and disease diagnoses via the output of multiple biophysical signals. However, it is still a challenge to fabricate short-peptide-based strain sensors. Here, we prepared a novel polymer-dipeptide double-network hydrogel with excellent stretchability, responsiveness, and stability. The poly(acrylic acid) (PAA) gel, by cross-linking, maintains mechanical and flexible properties, and the fluorenyl methoxycarbonyl-diphenylalanine (Fmoc-FF) network, by non-covalent interactions, is helpful for energy dissipation. With increasing tensile or compression strains, the PAA/Fmoc-FF hydrogel exhibited a high mechanical strength and fast recovery. Moreover, as the presence of KCl improves the electronic conductivity, the hybrid gel exhibited a cyclic strain-stress performance, which is the foundation of a strain sensor. Based on that, its application as a motion sensor was demonstrated by monitoring the movements of human joints, such as the forefinger, wrist, elbow, and knee. Consequently, the hybrid polymer-peptide gel could be an ideal candidate for wearable sensors in the future.

Understanding the influence of surfactants on the assembly of peptides has a considerable practical motivation. In this paper, we systematically study the anionic surfactant-assisted assembly of diphenylalanine (FF). FF forms broom-like structures in a concentration of sodium cholate (NaC) around the CMC, and assembles into linear and unidirectional rods in the presence of low and high surfactant concentrations. FF’s improved hydrogen bonding and controlled assembly rates are appropriate for other anionic surfactants. At this stage, the use of FF as the simplest protein consequence can be helpful in the investigation of further protein–surfactant interactions.