Yongli Zheng

Cytomimetic Large-Scale Vesicle Aggregation and Fusion Based on Host–Guest Interaction

Herein, we have shown a large-scale cell-mimetic (cytomimetic) aggregation process by using cell-sized polymer vesicles as the building blocks and intervesicular host-guest molecular recognition interactions as the driving force. We first prepared the hyperbranched polymer vesicles named branched polymersomes (BPs) around 5-10 μm through the aqueous self-assembly of a hyperbranched multiarm copolymer of HBPO-star-PEO [HBPO = hyperbranched poly(3-ethyl-3-oxetanemethanol); PEO = poly(ethylene oxide)]. Subsequently, adamantane-functionalized BPs (Ada-BPs) or β-cyclodextrin-functionalized BPs (CD-BPs) were prepared through the coassembly of HBPO-star-PEO and Ada-modified HBPO-star-PEO (HBPO-star-PEO-Ada), or of HBPO-star-PEO and CD-modified HBPO-star-PEO (HBPO-star-PEO-CD), respectively. Macroscopic vesicle aggregates were obtained by mixing CD-BPs and Ada-BPs. The intervesicular host-guest recognition interactions between β-CD units in CD-BPs and Ada units in Ada-BPs, which were proved by (1)H nuclear Overhauser effect spectroscopy (NOESY) spectrum and the fluorescence probe method, are responsible for the vesicle aggregation. Additionally, the vesicle fusion events happened frequently in the process of vesicle aggregation, which were certified by double-labeling fluorescent assay, real-time observation, content mixing assay, and component mixing assay.

Protein-Framed Multi-Porphyrin Micelles for a Hybrid Natural-Artificial Light-Harvesting Nanosystem.

A micelle-like hybrid natural-artificial light-harvesting nanosystem was prepared through protein-framed electrostatic self-assembly of phycocyanin and a four-armed porphyrin star polymer. The nanosystem has a special structure of pomegranate-like unimolecular micelle aggregate with one phycocyanin acceptor in the center and multiple porphyrin donors in the shell. It can inhibit donor self-quenching effectively and display efficient transfer of excitation energy (about 80.1 %) in water. Furthermore, the number of donors contributing to a single acceptor could reach as high as about 179 in this nanosystem.

Construction of Macroscopic Cytomimetic Vesicle Aggregates Based on Click Chemistry: Controllable Vesicle Fusion and Phase Separation

Vesicle-vesicle aggregation to mimic cell-cell aggregation has attracted much attention. Here, hyperbranched polymer vesicles (branched-polymersomes, BPs) with a cell-like size were selected as model membranes, and the vesicle aggregation process, triggered by click chemistry of the copper-catalysed azide-alkyne cycloaddition reaction, was systematically studied. For this purpose, azide and alkynyl groups were loaded on the membranes of BPs through the co-assembly method to obtain N(3)-BPs and Alk-BPs, respectively. Subsequently, macroscopic vesicle aggregates were obtained when these two kinds of functional BPs were mixed together with the ratio of azide to alkynyl groups of about 1:1. Both the vesicle fusion events and lateral phase separation on the vesicle membrane occurred during such a vesicle aggregation process, and the fusion rate and phase-separation degree could be controlled by adjusting the clickable group content. The vesicle aggregation process with N(3) -micelles as desmosome mimics to connect with Alk-BPs through click-chemistry reaction was also studied, and large-scale vesicle aggregates without vesicle fusion were obtained in this process. The present work has extended the controllable cytomimetic vesicle aggregation process with the use of covalent bonds, instead of noncovalent bonds, as the driving force.

Hyperbranched Multiarm Copolymers with a UCST Phase Transition: Topological Effect and the Mechanism

A novel thermoresponsive hyperbranched multiarm copolymer with a hydrophobic hyperbranched poly[3-ethyl-3-(hydroxymethyl)oxetane] core and many poly(acrylamide- co-acrylonitrile) (P(AAm- co-AN)) arms was for the first time synthesized through a reversible addition-fragmentation chain-transfer polymerization. These copolymers show reversible, sharp, and controlled temperature-responsive phase transitions at the upper critical solution temperature (UCST) in water and electrolyte solution. It is the first report on the hyperbranched copolymers with a UCST transition. Two series copolymers with variable AN content (series A) and variable arm length (series B) were synthesized to study the influence of molecular structure on the UCST transition. It was found that the UCST of copolymers could be raised by increasing the AN content or decreasing the arm length. Most interestingly, the amplification effect of the hyperbranched topological structure leads to a broad change of the UCST from 33.2 to 65.2 °C with the little change of AN content (5.9%). On the basis of variable temperature nuclear magnetic resonance, dynamic light scattering, and transmission electron microscopy, a UCST transition mechanism, in combination with hydrophilic/hydrophobic balance and multimicelle aggregate (MMA), was proposed. This work enriches the UCST copolymer topology and may extend the knowledge on the structure-activity relationship as well as the mechanism of the UCST polymers.

Construction of Light‐Harvesting Polymeric Vesicles in Aqueous Solution with Spatially Separated Donors and Acceptors

This communication describes polymer vesicles self-assembled from hyperbranched polymers (branched polymersomes (BPs)) as scaffolds, conceptually mimicking the natural light-harvesting system in aqueous solution. The system is constructed with hydrophobic 4-chloro-7-nitro-2,1,3-benzoxadiazole (NBD-Cl) as donors encapsulated in the hydrophobic hyperbranched cores of the vesicles and the hydrophilic Rhodamine B (RB) as acceptors incorporated on the surface of the vesicles through the cyclodextrin (CD)/RB host-guest interactions, through which the donors and acceptors are spatially separated to effectively avoid the self-quenching between donors. This vesicular light harvesting system has presented good energy transfer efficiency of about 80% in water, and can be used as the ink to write multiclolor letters. In addition, due to the giant dimension of BPs, the real-time fluorescent images of the vesicles under an optical microscope can be observed to prove the light-harvesting process. It is supposed that such a vesicular light-harvesting antenna can be used to construct artificial photosynthesis systems in the future.