Cell-Mimic Directional Cargo Transportation in a Visible-Light-Activated Colloidal Motor/Lipid Tube System.

Active tether and transportation of cargoes on cytoskeletal highway enabled by molecular motors is key for accurate delivery of vesicles and organelles in the complex intracellular environment. Here, a hybrid system composed of colloidal motors and self-assembled lipid tubes is designed to mimic the subcellular traffic system in living cells. The colloidal motors, composed of gold-coated hematite, display light-activated self-propulsion tunable by the light intensity and the concentration of hydrogen peroxide fuel. Importantly, the motors show light-switchable binding with lipid cargoes and attachment to the lipid tubes, whereby the latter act as the motor highways. Upon assembly, the colloidal motor/lipid tube system demonstrates directional delivery of lipid vesicles, emulating intracellular transportation. The assembly and function of the hybrid system are rationalized by a cooperative action of light-triggered electrophoretic and hydrodynamic effects, supported by finite element analysis. A synthetic analog of the biological protein motor/cytoskeletal filament system is realized for the manipulation and delivery of different matter at the microscale, which is expected to be a promising platform for various applications in materials science, nanotechnology, microfluidics, and synthetic biology.

Inorganic-Organic Hybrid Copolymeric Colloids as Multicolor Emission, Fuel-Free, UV- and Visible-Light-Actuated Micropumps.

Light-actuated micromachines are of enormous interest due to their ability to harvest light for triggering catalytic reactions to acquire free energy for mechanical work. This work presents an inorganic-organic hybrid copolymeric poly(cyclotriphosphazene-co-barbituric acid) colloid, which displays multiwavelength excited emission and catalytic activities, exploiting the unique structural, chemical, and optical features of inorganic heterocyclic ring hexachlorocyclotriphosphazene and organic co-monomer barbituric acid. Specifically, this work reveals particle-resolved unusual multicolor emission under excitation with the same or different wavelengths of light using fluorescence microscopy. The result is rationalized by density functional theory studies. In this work, the authors find that emission is coincident with fluorometric measurements, and the photocatalytic properties are anticipated from the overall band structure. This work also demonstrates the use of these colloids as micropumps, which can be remotely activated by UV, blue, and green lights under fuel-free conditions, and ascribe the behavior to ionic diffusiophoresis arising from light-triggered generation of H+ and other charged species. This work offers a new class of polymeric colloids with multiple-wavelength excited emission and catalytic activities, which is expected to open new opportunities in the design of fuel-free, photo-actuated micromachines and active systems.

Micrometer-size double-helical structures from phospholipid-modified carbon nanotubes.

Biomolecular self-assembly plays a key role in the life system. Herein, double-helical phospholipid-modified carbon nanotube structures were constructed via the self-assembly of phospholipids on carbon nanotubes. These micrometer size spring structures may find potential applications in biocompatible microrobots.

Corrigendum: Self Organization of Binary Colloidal Mixtures via Diffusiohporesis.

[This corrects the article DOI: 10.3389/fchem.2022.803906.].

Self-Organization of Binary Colloidal Mixtures via Diffusiophoresis.

Catalytic activity of the colloids and chemotactic response to gradients of the chemicals in the solution leads to effective interaction between catalytic colloids. In this paper, we simulate mixtures of active and passive colloids via a Brownian dynamics algorithm. These particles interact via phoretic interactions, which are determined by two independent parameters, surface activity and surface mobility. We find rich dynamic structures by tuning passive colloids' surface mobility, size, and area fractions, which include schools of active colloids with exclusion zone, yolk/shell cluster, and stable active-passive alloys to motile clusters. Dynamical cluster can also be formed due to the nonreciprocity of the phoretic interaction. Increasing the size ratio of passive colloids to active colloids favors the phase separation of active and passive colloids, resulting in yolk/shell structure. Increasing the area fraction of active colloids tends to transfer from dynamical clusters into stable alloys. The simulated binary active colloid systems exhibit intriguing nonequilibrium phenomena that mimic the dynamic organizations of active/passive systems.

Prediction of the size of electroformed giant unilamellar vesicle using response surface methodology.

The production of giant unilamellar vesicles (GUVs) with specific size and structure has been a challenge on the design of quantitative biological assays in cell-mimetic micro-compartments. In this study, the effect of electroformation parameters (electric potential, frequency, and temperature) on the size of GUVs was investigated. Using response surface methodology based on Box-Behnken design, GUVs from neutral, positive and negative charges were formulated. The average diameter of GUVs was determined for each formulation. The acquired data of these GUVs were successfully fitted with quadratic regression models. These models were applied to visualize the parameters for ideal GUVs with wanted diameters by the obtained phase diagrams. These results show that response surface methodology can be used to estimate the electroformation parameters for specifically sized GUVs.

Electroformation of double vesicles using an amplitude modulated electric field.

Double vesicles are a promising model to mimic eukaryotic cells, yet effective preparation methods with high yields and stable double vesicles are scarce. Previously reported electroformation methods were mainly based on sinusoidal AC fields. Using a combination of sinusoidal and amplitude modulated (AM) electric fields lipid double vesicles could be produced for the first time by a simple electroformation process. First lipid domes formed in a sinusoidal AC field. The domes grew into tubes during the subsequent application of an AM field. These tubes deformed into double vesicles to minimize their free energy in accordance with the area-difference-elasticity model. Two forces are involved to explain the mechanism behind tube formation. The pulling force (F) is responsible to drag the domes into tubular vesicles, but has to overcome a critical force (Fc). The most important parameters of the electrical field were explored systematically. In our work, a maximum yield for double vesicles of 63% was achieved. These vesicles proved to be stable for one week at least. Hence our method could provide a way to fabricate novel cell models.