Mingxi Zhang

Chiral effect at protein/graphene interface: a bioinspired perspective to understand amyloid formation.

Protein misfolding to form amyloid aggregates is the main cause of neurodegenerative diseases. While it has been widely acknowledged that amyloid formation in vivo is highly associated with molecular surfaces, particularly biological membranes, how their intrinsic features, for example, chirality, influence this process still remains unclear. Here we use cysteine enantiomer modified graphene oxide (GO) as a model to show that surface chirality strongly influences this process. We report that R-cysteine modification suppresses the adsorption, nucleation, and fiber elongation processes of Aβ(1-40) and thus largely inhibits amyloid fibril formation on the surface, while S-modification promotes these processes. And surface chirality also greatly influences the conformational transition of Aβ(1-40) from α-helix to β-sheet. More interestingly, we find that this effect is highly related to the distance between chiral moieties and GO surface, and inserting a spacer group of about 1-2 nm between them prevents the adsorption of Aβ(1-40) oligomers, which eliminates the chiral effect. Detailed study stresses the crucial roles of GO surface. It brings novel insights for better understanding the amyloidosis process on surface from a biomimetic perspective.

Dual-Responsive Gold Nanoparticles for Colorimetric Recognition and Testing of Carbohydrates with a Dispersion-Dominated Chromogenic Process.

A dispersion-dominated colorimetric approach for the recognition of carbohydrates based on biomolecule-responsive AuNPs is presented. Taking advantage of the unique dual-responsiveness of smart copolymers, the aggregation and dispersion of AuNPs can be modulated by both temperature and different kinds of carbohydrates, giving rise to a novel chromogenic mechanism for the recognition and testing of carbohydrates in aqueous media.

Dynamic Biointerfaces: From Recognition to Function

The transformation of recognition signals into regulating macroscopic behaviors of biological entities (e.g., biomolecules and cells) is an extraordinarily challenging task in engineering interfacial properties of artificial materials. Recently, there has been extensive research for dynamic biointerfaces driven by biomimetic techniques. Weak interactions and chirality are two crucial routes that nature uses to achieve its functions, including protein folding, the DNA double helix, phospholipid membranes, photosystems, and shell and tooth growths. Learning from nature inspires us to design dynamic biointerfaces, which usually take advantage of highly selective weak interactions (e.g., synergetic chiral H-bonding interactions) to tailor their molecular assemblies on external stimuli. Biomolecules can induce the conformational transitions of dynamic biointerfaces, then drive a switching of surface characteristics (topographic structure, wettability, etc.), and eventually achieve macroscopic functions. The emerging progresses of dynamic biointerfaces are reviewed and its role from molecular recognitions to biological functions highlighted. Finally, a discussion is presented of the integration of dynamic biointerfaces with the basic biochemical processes, possibly solving the big challenges in life science.

Synthesis of sub-5 nm Au–Ag alloy nanoparticles using bio-reducing agent in aqueous solution

Bio-reducing agent NADPH with relatively weak reducibility and favourable structure simultaneously reduced Au and Ag ions into sub-5 nm alloy nanoparticles in aqueous solution at room temperature.

Intermediate-dominated controllable biomimetic synthesis of gold nanoparticles in a quasi-biological system

A new biomimetic strategy of creating a quasi-biological system (an aqueous solution containing electrolytes, peptide, enzyme and coenzyme) for the preparation of gold nanoparticles with uniform and tunable sizes has been put forward and validated, adopting environmentally-friendly reducing agents and a biocompatible capping ligand in aqueous solution at room temperature. The biomimetic synthetic route has the characteristics for good stability of the resulting AuNPs capped with glutathione via strong Au-S bond in aqueous solution, an appropriate composition of the intermediate with a redox potential favorable for the biomimetic reduction under mild conditions, suitable pH values to adjust the rate of the reduction, and the addition of enzyme catalyzing the reduction. By only adjusting the concentration of the reducing agent NADPH, a series of AuNPs with narrow size-distribution could be controllably synthesized. This method of rational utilization of biological processes could provide a new way for the sustainable development of nanotechnology.

Chiral polymer-based biointerface materials

Chirality is a unique phenomenon in nature. Chiral interactions play an important role in biological and physiological processes, which provides much inspiration for scientists to develop chiral materials. As a breakthrough from traditional materials, biointerface materials based on chiral polymers have attracted increasing interest over the past few years. Such materials elegantly combine the advantages of chiral surfaces and traditional polymers, and provide a novel solution not only for the investigation of chiral interaction mechanisms but also for the design of biomaterials with diverse applications, such as in tissue engineering and biocompatible materials, bioregulation, chiral separation and chiral sensors. Herein, we summarize recent advances in the study of chiral effects and applications of chiral polymer-based biointerface materials, and also present some challenges and perspectives.