Thursday, November 22, 2018

Nature Chemistry Contents December 2018 Volume 10 Number 12

Nature Chemistry

TABLE OF CONTENTS

December 2018 Volume 10, Issue 12

News & Views
Articles
Amendments & Corrections
In Your Element

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News & Views

Exploiting evolution    p1173
Kathryn Ashe
doi:10.1038/s41557-018-0183-8

Redox activity goes organic    pp1173 - 1175
Diane E. Cabelli
doi:10.1038/s41557-018-0180-y

The wetter the better    pp1175 - 1177
Tanmay Banerjee & Bettina V. Lotsch
doi:10.1038/s41557-018-0176-7

Magnetic control of a reaction path    pp1177 - 1179
Astrid Bergeat & Christian Naulin
doi:10.1038/s41557-018-0177-6

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Articles

Sulfone-containing covalent organic frameworks for photocatalytic hydrogen evolution from water    pp1180 - 1189
Xiaoyan Wang, Linjiang Chen, Samantha Y. Chong, Marc A. Little, Yongzhen Wu et al.
doi:10.1038/s41557-018-0141-5

The inherent synthetic tuneability of organic materials makes them attractive in photocatalysis, but they tend to have low quantum efficiencies for water splitting. A crystalline covalent organic framework featuring a benzo-bis(benzothiophene sulfone) moiety has now been shown to exhibit high activity for photochemical hydrogen evolution from water.

Quantum-state-controlled channel branching in cold Ne(3P2)+Ar chemi-ionization    pp1190 - 1195
Sean D. S. Gordon, Juan J. Omiste, Junwen Zou, Silvia Tanteri, Paul Brumer et al.
doi:10.1038/s41557-018-0152-2

Steric effects in a fundamental energy-transfer reaction at collision energies from over 1,000 K down to 20 mK have now been studied. At high energies a pronounced dependence of the reactivity on the reactant orientation is observed, but this effect is not present at the lowest energies because of dynamic reorientation.

A crystalline monosubstituted carbene    pp1196 - 1200
Ryo Nakano, Rodolphe Jazzar & Guy Bertrand
doi:10.1038/s41557-018-0153-1

So far, monosubstituted carbenes have only been spectroscopically characterized at very low temperatures. Now, it has been shown that a bulky, chemically inert, amino substituent is enough to tame the intrinsic tendency of carbenes towards dimerization, enabling their isolation at room temperature.

A genetically encoded photosensitizer protein facilitates the rational design of a miniature photocatalytic CO2-reducing enzyme    pp1201 - 1206
Xiaohong Liu, Fuying Kang, Cheng Hu, Li Wang, Zhen Xu et al.
doi:10.1038/s41557-018-0150-4

A 27 kDa photosensitizer protein (PSP) has now been developed and used to design a miniature photocatalytic CO2-reducing enzyme. Visible light drives the PSP efficiently to the long-lived triplet excited state (PSP*), and then to a super-reducing radical (PSP), which is strong enough to reduce many CO2-reducing catalysts. The 3D structure of PSP at 1.8 Å resolution was determined by X-ray crystallography.

Superoxide dismutase activity enabled by a redox-active ligand rather than metal    pp1207 - 1212
Meghan B. Ward, Andreas Scheitler, Meng Yu, Laura Senft, Annika S. Zillmann et al.
doi:10.1038/s41557-018-0137-1

Catalytic superoxide dismutase mimics typically involve manganese centres. Now, a complex based on redox-inactive zinc(ii) and a redox-active quinol ligand is found to catalytically degrade superoxide. The reaction, proposed to occur through oxidation of the ligand to a quinoxyl radical, is hastened rather than inhibited by the presence of phosphate.

Inhibiting amyloid-β cytotoxicity through its interaction with the cell surface receptor LilrB2 by structure-based design    pp1213 - 1221
Qin Cao, Woo Shik Shin, Henry Chan, Celine K. Vuong, Bethany Dubois et al.
doi:10.1038/s41557-018-0147-z

Inhibiting the interaction between amyloid-β (Aβ) and a neuronal cell surface receptor, LilrB2, could offer a potential route for treating Alzheimer's disease. Now, binding sites between Aβ and LilrB2 have been discovered and computational selection has identified inhibitors that block this binding site. Cell-penetrating inhibitors were found to block the Aβ–LilrB2 interaction and limit Aβ-induced cytotoxicity.

Carbohydrate stabilization extends the kinetic limits of chemical polysaccharide depolymerization    pp1222 - 1228
Ydna M. Questell-Santiago, Raquel Zambrano-Varela, Masoud Talebi Amiri & Jeremy S. Luterbacher
doi:10.1038/s41557-018-0134-4

Chemically depolymerizing biomass polysaccharides to simple sugars is often controlled by the balance between depolymerization and degradation kinetics, which has limited the concentration of solutions that can be obtained and overall yields. The reversible stabilization of carbohydrates by acetal formation pushes back these limits and creates stabilized sugars that have advantageous properties for further upgrading.

Catalytic dehydrogenative decarboxyolefination of carboxylic acids    pp1229 - 1233
Xiang Sun, Junting Chen & Tobias Ritter
doi:10.1038/s41557-018-0142-4

A direct conversion of carboxylic acids to alpha-olefins without the need for a stoichiometric additive has now been reported. The transformation is enabled by a dual cobalt/iridium proton-reduction–photoredox catalyst system, and can proceed on abundant fatty acids as well as on complex carboxylic acids.

Mining the cellular inventory of pyridoxal phosphate-dependent enzymes with functionalized cofactor mimics    pp1234 - 1245
Annabelle Hoegl, Matthew B. Nodwell, Volker C. Kirsch, Nina C. Bach, Martin Pfanzelt et al.
doi:10.1038/s41557-018-0144-2

A chemical proteomic strategy has now been developed for profiling pyridoxal-phosphate dependent enzymes (PLP-DEs) in cells. Pyridoxal-based probes are phosphorylated in situ and bind to cellular PLP-DEs as cofactor mimics. The method accessed 73% of the Staphylococcus aureus PLP-dependent proteome and annotated uncharacterized proteins as novel PLP-DEs.

Spontaneous doping of the basal plane of MoS2 single layers through oxygen substitution under ambient conditions    pp1246 - 1251
János Pető, Tamás Ollár, Péter Vancsó, Zakhar I. Popov, Gábor Zsolt Magda et al.
doi:10.1038/s41557-018-0136-2

MoS2 single layers spontaneously undergo a slow oxygen substitution reaction under ambient conditions giving rise to solid-solution-type 2D molybdenum oxy-sulfide crystals. The oxygen substitution sites of the 2D MoS2xOx crystals act as efficient single-atom catalytic centres for the hydrogen evolution reaction.

Cavitation energies can outperform dispersion interactions    pp1252 - 1257
Suhang He, Frank Biedermann, Nina Vankova, Lyuben Zhechkov, Thomas Heine et al.
doi:10.1038/s41557-018-0146-0

Binding interactions, whether between a biological receptor and ligand or between a synthetic host and guest, are frequently stronger for larger molecules than for smaller ones. This is commonly believed to arise from increased dispersion interactions, but it has now been shown that cavitation energies—always required to dissolve molecules in solution—can be more important.

5-Formylcytosine organizes nucleosomes and forms Schiff base interactions with histones in mouse embryonic stem cells    pp1258 - 1266
Eun-Ang Raiber, Guillem Portella, Sergio Martínez Cuesta, Robyn Hardisty, Pierre Murat et al.
doi:10.1038/s41557-018-0149-x

A series of in vitro and in vivo studies has now shown that 5fC is linked to increased nucleosome occupancy and stability. Moreover, there is evidence that Schiff base formation between histones and 5fC impacts RNA polymerase II transcription activity in mouse embryonic stem cells.

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Amendments & Corrections

Author Correction: Inhibiting amyloid-β cytotoxicity through its interaction with the cell surface receptor LilrB2 by structure-based design    p1267
Qin Cao, Woo Shik Shin, Henry Chan, Celine K. Vuong, Bethany Dubois et al.
doi:10.1038/s41557-018-0182-9

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In Your Element

Promethium puzzles    p1270
Stuart Cantrill
doi:10.1038/s41557-018-0179-4

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