A constitutional isomeric library synthesized by a modular approach has been used to discover six amphiphilic Janus dendrimer primary structures, which self-assemble into uniform onion-like vesicles with predictable dimensions and number of internal bilayers. These vesicles, denoted onion-like dendrimersomes, are assembled by simple injection of a solution of Janus dendrimer in a water-miscible solvent into water or buffer. These dendrimersomes provide mimics of double-bilayer and multibilayer biological membranes with dimensions and number of bilayers predicted by the Janus compound concentration in water. The simple injection method of preparation is accessible without any special equipment, generating uniform vesicles, and thus provides a promising tool for fundamental studies as well as technological applications in nanomedicine and other fields.synthetic membranes | biomembrane mimics | multibilayer vesicles M ost living organisms contain single-bilayer membranes composed of lipids, glycolipids, cholesterol, transmembrane proteins, and glycoproteins (1). Gram-negative bacteria (2, 3) and the cell nucleus (4), however, exhibit a strikingly special envelope that consists of a concentric double-bilayer membrane. More complex membranes are also encountered in cells and their various organelles, such as multivesicular structures of eukaryotic cells (5) and endosomes (6), and multibilayer structures of endoplasmic reticulum (7,8), myelin (9, 10), and multilamellar bodies (11,12). This diversity of biological membranes inspired corresponding biological mimics. Liposomes ( Fig. 1) self-assembled from phospholipids are the first mimics of singlebilayer biological membranes (13-16), but they are polydisperse, unstable, and permeable (14). Stealth liposomes coassembled from phospholipids, cholesterol, and phospholipids conjugated with poly(ethylene glycol) exhibit improved stability, permeability, and mechanical properties (17)(18)(19)(20). Polymersomes (21-24) assembled from amphiphilic block copolymers exhibit better mechanical properties and permeability, but are not always biocompatible and are polydisperse. Dendrimersomes (25-28) self-assembled from amphiphilic Janus dendrimers and minidendrimers (26-28) have also been elaborated to mimic single-bilayer biological membranes. Amphiphilic Janus dendrimers take advantage of multivalency both in their hydrophobic and hydrophilic parts (23,(29)(30)(31)(32). Dendrimersomes are assembled by simple injection (33) of a solution of an amphiphilic Janus dendrimer (26) in a water-soluble solvent into water or buffer and produce uniform (34), impermeable, and stable vesicles with excellent mechanical properties. In addition, their size and properties can be predicted by their primary structure (27). Amphiphilic Janus glycodendrimers self-assemble into glycodendrimersomes that mimic the glycan ligands of biological membranes (35). They have been demonstrated to be bioactive toward biomedically relevant bacterial, plant, and human lectins, and could have numerous applications i...

An accelerated modular synthesis produced 18 amphiphilic Janus glycodendrimers with three different topologies formed from either two or one carbohydrate head groups or a mixed constellation with a noncarbohydrate hydrophilic arm. By simple injection of their THF solutions into water or buffer, all of the Janus compounds self-assembled into uniform, stable, and soft unilamellar vesicles, denoted glycodendrimersomes. The mixed constellation topology glycodendrimersomes were demonstrated to be most efficient in binding plant, bacterial, and human lectins. This evidence with biomedically relevant receptors offers a promising perspective for the application of such glycodendrimersomes in targeted drug delivery, vaccines, and other areas of nanomedicine.

A library of eight amphiphilic Janus glycodendrimers (GDs) with D-mannose (Man) headgroups, a known routing signal for lectinmediated transport processes, was constructed via an iterative modular methodology. Sequence-defined variations of the Janus GD modulate the surface density and sequence of Man after selfassembly into multilamellar glycodendrimersomes (GDSs). The spatial mode of Man presentation is decisive for formation of either unilamellar or onion-like GDS vesicles. Man presentation and Janus GD concentration determine GDS size and number of bilayers. Beyond vesicle architecture, Man topological display affects kinetics and plateau level of GDS aggregation by a tetravalent model lectin: the leguminous agglutinin Con A, which is structurally related to endogenous cargo transporters. The agglutination process was rapid, efficient, and readily reversible for onion-like GDSs, demonstrating their value as versatile tools to explore the nature of physiologically relevant glycan/lectin pairing.self-assembly | synthetic multilamellar vesicles | glycolipid mimics S upramolecular chemistry has enormous potential to help resolve fundamental questions in the realm of cell biology. One of the key challenges is the design of programmable models for vesicles and cells and their surfaces as a means of establishing a chemical platform that mimics natural features in size and shape, and also allows customized implementation of bioactive epitopes, in structural and topological terms. Natural complexity can conveniently be reduced to simple systems, whose degree of diversity can then be rationally reconstituted in a stepwise process. Focusing on surface properties, the recently gained access to uniform populations of stable glycodendrimersomes (GDSs) by a simple injection method using a solution of amphiphilic Janus glycodendrimers (GDs) as building blocks for self-assembly in a water-soluble aprotic solvent (1-3), has afforded a promising opportunity to realize this concept. Interestingly, the resulting GDSs, which have tunable surface features, can cover the size range of naturally occurring vesicles such as endo-and exosomes.

Despite the growing interest of quantum dots (QDs) in biological applications, there are many concerns regarding the potential accumulation and toxic effects of Cd-containg QDs in animals and humans. Zinc oxide QDs are promising alternatives for diagnosis and imaging but their aqueous instability has markedly limited their use. Generations 1, 2 and 3 (noted G1, G2, and G3, respectively) of new poly(amidoamine) (PAMAM) dendrons bearing a siloxane group at the focal point were prepared from 3-aminopropyltrimethoxysilane. Using tetramethylammonium hydroxide as cross-linking agent, hydrophobic oleate-capped ZnO QDs were functionalized with G1 or G2 dendrons, as evidenced by FT-IR, UV-visible and XPS analyses, and were successfully transferred in aqueous solution. AFM and TEM images show that ZnO@G1 and ZnO@G2 QDs have a spherical shape with average crystalline sizes of 5.3 and 5.1 nm, respectively. Immediately after dispersion in water, ZnO@G1 and ZnO@G2 QDs exhibit a broad and strong visible emission peak centered at 550 nm with a quantum yield of ca. 18%. A strong increase of photoluminescence quantum yields was observed over time and values up to 59% could be reached after ca. 20 days of storage in water at room temperature. The good quantum yields and the stabilities of PAMAMdendron capped ZnO QDs ensured their potential applications in cell imaging. ZnO@G2 were successfully used for the labelling of the Gram + bacterium Staphylococcus aureus. The biocompatibility of these QDs is markedly improved compared to Cd-based ones as growth inhibition tests showed that ZnO@G2 QDs could be used with concentrations up to 1 mM without altering the cell growth of the Escherichia coli bacterium while most Cd-containing QDs exhibit cytotoxicity already at the nM level. .

Surface-presented glycans (complex carbohydrates) are docking sites for adhesion/growth-regulatory galectins within cell-cell/ matrix interactions. Alteration of the linker length in human galectin-8 and single-site mutation (F19Y) are used herein to illustrate the potential of glycodendrimersomes with programmable glycan displays as a model system to reveal the functional impact of natural sequence variations in trans recognition. Extension of the linker length slightly reduces lectin capacity as agglutinin and slows down aggregate formation at low ligand surface density. The mutant protein is considerably less active as agglutinin and less sensitive to low-level ligand presentation. The present results suggest that mimicking glycan complexity and microdomain occurrence on the glycodendrimersome surface can provide key insights into mechanisms to accomplish natural selectivity and specificity of lectins in structural and topological terms.adhesion | agglutination | glycobiology | membrane mimic | self-assembly