The present review focuses on the proteins and peptides at the interfaces of nanostructured metals and semiconductors as a result of their use in synthesis in-situ and functionalization of nanostructures. We start the review with an introduction about the peculiar properties of nanostructured materials and their applications. In the following, the chemical and structural properties of peptides and proteins that allow their use as reducing, stabilizing, and functionalization agents are discussed. Proteins and peptides have not only the chemical groups for the metal ion reducing but also provide templates for directing the crystalline growing of nanostructures to the desired shapes and sizes. Proteins and peptides are also used mainly for the stabilization and functionalization of a diversity of nanostructured materials providing properties such as biocompatibility, plasmon-enhanced catalysis, sensing, micro/nanomotors, spin filters, and others. Nanostructured materials of metal oxides have mainly been functionalized with proteins and peptides to gain specific properties such as light harvesting and spin filters. Herein, we described the synthesis and functionalization of some types of nanostructured materials by using peptides and proteins. In the last part of the review, it is discussed the perspectives and challenges for the use of proteins and peptides in Nanotechnology.

Liposomes containing magnetic nanoparticles (magnetoliposomes) have been extensively explored for targeted drug delivery. However, the magnetic effect of nanoparticles movement is also an attractive choice for the conduction of signals in communication systems at the nanoscale level because of the simple manipulation and efficient control. Here, we propose a model for the transmission of electrical and luminous signals taking advantage of magnetophoresis. The study involved three steps. Firstly, magnetite was synthesized and incorporated into fusogenic large unilamellar vesicles (LUVs) previously associated with a fluorescent label. Secondly, the fluorescent magnetite-containing LUVs delivered their contents to the giant unilamellar vesicles (GUVs), which were corroborated by magnetophoresis and fluorescence microscopy. In the third step, magnetophoresis of magnetic vesicles was used for the conduction of the luminous signal from a capillary to an optical fibre connected to a fluorescence detector. Also, the magnetophoresis effects on subsequent transmission of the electrochemical signal were demonstrated using magnetite associated with CTAB micelles modified with ferrocene. We glimpse that these magnetic supramolecular systems can be applied in micro- and nanoscale communication systems.

Ciprofloxacin hydrochloride (CIPRO) is considered an emerging pollutant in aquatic environments with the capacity to disseminate antibiotic resistance. Considering the pro-oxidant potential of ZnO and Cu-doped ZnO (Cu-ZnO) wurtzite crystals, the potential Ciprofloxacin photodegradation by these materials was investigated. CIPRO titration with ZnO and Cu-ZnO promoted the formation of zinc complexes and ~4% antibiotic adsorption. The carboxylic groups of CIPRO can complex Zn 2+ by promoting the nanoetching of ZnO and Cu-ZnO crystallite surfaces. The alkaline interfaces provided by ZnO create a microenvironment favorable for Zn 2+ chelation by CIPRO carboxylates. The photodegradation degree was similar for CIPRO and CIPRO-Zn under UV light, as revealed by UV-visible spectroscopy and FTIR. Therefore, the ZnO and Cu-ZnO crystals contributed to the formation of CIPRO-Zn rather than the photo-oxidative degradation of the antibiotic. Considering that CIPRO-Zn chelates disfavor bacterial selection for resistance, the treatment of CIPRO-contaminated effluents with ZnO and Cu-ZnO can facilitate desirable metal chelation without impairing photodegradation.

Graphic abstract Bioluminescent gold nanoparticles (AuNPs) were synthesized in situ using dithiol-terminated polyethylene glycol (PEG(SH) 2 ) as reducer and stabilizing agents. Hybrid Au/F 3 O 4 nanoparticles were also produced in a variation of synthesis, and both types of nanostructures had the polymer capping replaced by l -cysteine (Cys). The four types of nanoparticles, PEG(SH) 2 AuNPs, PEG(SH) 2 Au/F 3 O 4 NPs, CysAuNPs, and CysAu/F 3 O 4 NPs were associated with purified recombinant Pyrearinus termitilluminans green emitting click beetle luciferase (PyLuc) and Phrixotrix hirtus (RELuc) red-emitting railroad worm luciferase. Enzyme association with PEG(SH) 2 was also investigated as a control. Luciferases were chosen because they catalyze bioluminescent reactions used in a wide range of bioanalytical applications, including ATP assays, gene reporting, high-throughput screening, bioluminescence imaging, biosensors and other bioluminescence-based assays. The immobilization of PyLuc and RELuc promoted partial suppression of the enzyme luminescence activity in a functionalization-dependent way. Association of PyLuc and RELuc with AuNPs increased the enzyme operational stability in relation to the free enzyme, as evidenced by the luminescence intensity from 0 to 7 h after substrate addition. The stability of the immobilized enzymes was also functionalization-dependent and the association with CysAuNPs was the condition that combined more sustained luminescent activity with a low degree of luminescence quenching. The higher enzymatic stability and sustained luminescence of luciferases associated with nanoparticles may improve the applicability of bioluminescence for bioimaging and biosensing purposes. Supplementary Information The online version contains supplementary material available at 10.1007/s43630-021-00111-0.