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Mass production at the nanoscale requires molecular machines that can control, with high fidelity, the spatial orientation of other reactive species. The demonstration of a synthetic system in which a molecular robotic arm can be used to manipulate the position of a chemical cargo is a significant step towards achieving this goal.
Incorporation of a π-clamp—a four-residue sequence (Phe-Cys-Pro-Phe)—into a protein enables the site-specific modification of the π-clamp cysteine side-chain. The π-clamp can be genetically encoded and does not require protecting-groups or catalysts to provide selective conjugation.
The selective conversion of abundant and inexpensive alkane feedstocks into value-added speciality chemicals is a significant and challenging goal, and methods for catalytically converting alkanes into useful linear alkylsilanes are unknown, to date. Now, a strategy combining alkane dehydrogenation with regioselective olefin isomerization–hydrosilylation to produce linear alkylsilanes is described.
Factory assembly lines often feature robots that pick up, reposition and connect components in a programmed manner. Now, it has been shown that a molecular machine is able to pick up a cargo, reposition it, set it down and release it at a site approximately 2 nm away from the starting position.
Intracellular bodies called liquid organelles are rich in nucleic acids and proteins, and are thought to occur by liquid–liquid phase coexistence. Now, enzymatic control over the phosphorylation state of a simple cationic peptide, thereby altering its electrostatic interaction with RNA, has been shown to drive formation and dissolution of droplets that mimic these intracellular liquid bodies.
The encapsulation and stabilization of an oxygen tolerant [NiFe]-hydrogenase, sequestered within the bacteriophage P22 capsid, has now been achieved through a directed self-assembly process. Probing the catalytic activity and infrared spectroscopic signatures of the bio-inspired assembly shows that the capsid provides stability and protection to the hydrogenase cargo.
Supramolecular processes are attractive for the generation of functional materials, but managing multiple, competing self-assembly pathways has remained challenging. Now, the self-assembly of a platinum compound into three different aggregates has been elucidated, visualized in real time, and controlled.
Fullerene-based dendritic structures coated with 120 sugars can be made in high yields in a relatively short sequence of reactions. The mannosylated compound is shown to inhibit Ebola infection in cells more efficiently than monofullerene-based glycoclusters.
γ-Butyrolactone is a biomass-derived cyclic ester that is commonly thought to be non-polymerizable. Now, exploiting the thermodynamics of polymer formation and careful control of the reaction conditions has made this possible leading to high-molecular-weight products and control of polymer topology.
Little is known about how the identity of a leaving group affects the dynamics of a bimolecular nucleophilic substitution reaction. A study of the reaction of F− with CH3Cl, and comparison to its reaction with CH3I, now reveals key insights into such effects, with reactant orientation considered a key factor in understanding the behaviour observed.
A wide range of different aqueous chemistries for the site-selective modification of proteins have been described over the past decade. This Perspective discusses the scope and potential of chemical site-selective protein-modification methods in the context of their biological and therapeutic applications.
Doping mesoporous materials is an attractive way to tune their properties, but typically disrupts the host materials’ structures. Ultrasmall graphitic pencil nanodots have now been prepared, doped with heteroatoms, and inserted in a well-dispersed manner within the ordered structure of mesoporous materials including TiO2, carbon and silica, by a co-assembly approach.
The catalytic activity of a rotaxane incorporating a gold(I) centre can be switched on by the addition of a guest ion that can bind inside the macrocyclic cavity of the system. The nature of the guest can also influence the selectivity of the catalyst, reminiscent of allosteric modulation in enzymes.
A synthetic receptor has been designed to form pseudorotaxanes and polypseudorotaxanes with oligo/polysaccharides in water. Target substrates have all-equatorial substitution patterns, and include cellulose, cellodextrins and the cationic polysaccharide chitosan. The results suggest an approach to dissolving these polysaccharides under mild conditions and could prove useful for processing these abundant renewable resources.
Glycosyl cations are universally accepted as key intermediates in the mechanism of glycosylation—the reaction that covalently links carbohydrates to other molecules—but their high reactivity makes them difficult to characterize. Using HF/SbF5 superacid, two glucosyl cations have been generated and stabilized, then characterized by NMR spectroscopy aided by computation and their conformation elucidated.
Bio-derived γ-butyrolactone (γ-BL) is commonly referred to as ‘non-polymerizable’ due to its low strain energy. Now it has been shown that ring-opening polymerization of γ-BL can in fact proceed to high conversions under ambient pressure with a suitable catalyst, producing high-molecular-weight polymers with controlled topologies and complete recyclability.
