The causative agent of the COVID-19 pandemic, SARS-CoV-2, is steadily mutating during continuous transmission among humans. Such mutations can occur in the spike (S) protein that binds to the ACE2 receptor and is cleaved by TMPRSS2. However, whether S mutations affect SARS-CoV-2 cell entry remains unknown. Here, we show that naturally occurring S mutations can reduce or enhance cell entry via ACE2 and TMPRSS2. A SARS-CoV-2 S-pseudotyped lentivirus exhibits substantially lower entry than that of SARS-CoV S. Among S variants, the D614G mutant shows the highest cell entry, as supported by structural and binding analyses. Nevertheless, the D614G mutation does not affect neutralization by antisera against prototypic viruses. Taken together, we conclude that the D614G mutation increases cell entry by acquiring higher affinity to ACE2 while maintaining neutralization susceptibility. Based on these findings, further worldwide surveillance is required to understand SARS-CoV-2 transmissibility among humans.

Photocatalytic CO2 reduction is an effective means to generate renewable energy. It involves redox reactions, reduction of CO2 and oxidation of water, that leads to the production of solar fuel. Significant research effort has therefore been made to develop inexpensive and practically sustainable semiconductor‐based photocatalysts. The exploration of atomic‐level active sites on the surface of semiconductors can result in an improved understanding of the mechanism of CO2 photoreduction. This can be applied to the design and synthesis of efficient photocatalysts. In this review, atomic‐level reactive sites are classified into four types: vacancies, single atoms, surface functional groups, and frustrated Lewis pairs (FLPs). These different photocatalytic reactive sites are shown to have varied affinity to reactants, intermediates, and products. This changes pathways for CO2 reduction and significantly impacts catalytic activity and selectivity. The design of a photocatalyst from an atomic‐level perspective can therefore be used to maximize atomic utilization efficiency and lead to a high selectivity. The prospects for fabrication of effective photocatalysts based on an in‐depth understanding are highlighted.

Membrane-associated RING-CH 8 (MARCH8) is one of 11 members of the recently discovered MARCH family of RING (really interesting new gene)-finger E3 ubiquitin ligases. MARCH8 downregulates several host transmembrane proteins, including major histocompatibility complex (MHC)-II, CD86, interleukin (IL)-1 receptor accessory protein, TNF-related apoptosis-inducing ligand (TRAIL) receptor 1 and the transferrin receptor. However, its physiological roles remain largely unknown. Here we identify MARCH8 as a novel antiviral factor. The ectopic expression of MARCH8 in virus-producing cells does not affect levels of lentivirus production, but it does markedly reduce viral infectivity. MARCH8 blocks the incorporation of HIV-1 envelope glycoprotein into virus particles by downregulating it from the cell surface, probably through their interaction, resulting in a substantial reduction in the efficiency of viral entry. The inhibitory effect of MARCH8 on vesicular stomatitis virus G-glycoprotein is even more remarkable, suggesting a broad-spectrum inhibition of enveloped viruses by MARCH8. Notably, the endogenous expression of MARCH8 is high in monocyte-derived macrophages and dendritic cells, and MARCH8 knockdown or knockout in macrophages significantly increases the infectivity of virions produced by these cells. Our findings thus indicate that MARCH8 is highly expressed in terminally differentiated myeloid cells, and that it is a potent antiviral protein that targets viral envelope glycoproteins and reduces their incorporation into virions.

The electrochemical nitrogen reduction reaction (NRR) is a promising alternative to the energy‐intensive Haber–Bosch process for ammonia synthesis. Among the possible electrocatalysts, bismuth‐based materials have shown unique NRR properties due to their electronic structures and poor hydrogen evolution activity. However, identification of the active sites and reaction mechanism is still difficult due to structural and chemical changes under reaction potentials. Herein, in situ Raman spectroscopy, complemented by electron microscopy, is employed to investigate the structural and chemical transformation of the Bi species during the NRR. Nanorod‐like bismuth‐based metal–organic frameworks are reduced in situ and fragment into densely contacted Bi0 nanoparticles under the applied potentials. The fragmented Bi0 nanoparticles exhibit excellent NRR performance in both neutral and acidic electrolytes, with an ammonia yield of 3.25 ± 0 .08 µg cm−2 h−1 at −0.7 V versus reversible hydrogen electrode and a Faradaic efficiency of 12.11 ± 0.84% at −0.6 V in 0.10 m Na2SO4. Online differential electrochemical mass spectrometry detects the production of NH3 and N2H2 during NRR, suggesting a possible pathway through two‐step reduction and decomposition. This work highlights the importance of monitoring and optimizing the electronic and geometric structures of the electrocatalysts under NRR conditions.

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The conversion of water into clean hydrogen fuel using renewable solar energy can potentially be used to address global energy and environmental issues. However, semiconductorbased photocatalytic H 2 evolution from pure water splitting has low efficiency and poor stability. Hole scavengers are therefore added to boost separation efficiency of photo-excited electron-hole pairs and improve stability by consuming the strongly oxidative photo-excited holes. The drawbacks of this approach are an increased cost and production of waste. Recently, researchers have reported the use of abundantly available hole scavengers, including biomass, biomass-derived intermediates, plastic wastes, and a range of alcohols for H 2 evolution, coupled with value-added chemicals production using semiconductor-based photocatalysts. It is timely, therefore, to comprehensively summarize the properties, performances, and mechanisms of these photocatalysts, and critically review recent advances, challenges and opportunities in this emerging area. Herein, this paper: 1) outlines fundamental reaction mechanisms of photocatalysts for H 2 evolution coupled with selective oxidation, C-H activation and CC coupling, together with non-selective oxidation, using holescavengers; 2) introduces equations to compute conversion/selectivity of selective oxidation; 3) summarizes and critically compares recently reported photocatalysts with particular emphasis on correlation between physicochemical characteristics and performances, together with photocatalytic mechanisms, and; 4) appraises current advances and challenges.

Single-atom photocatalysts have demonstrated an enormous potential in producing value-added chemicals and/or fuels using sustainable and clean solar light to replace fossil fuels causing global energy and environmental issues. These photocatalysts not only exhibit outstanding activities, selectivity, and stabilities due to their distinct electronic structures and unsaturated coordination centers but also tremendously reduce the consumption of catalytic metals owing to the atomic dispersion of catalytic species. Besides, the single-atom active sites facilitate the elucidation of reaction mechanisms and understanding of the structure-performance relationships. Presently, apart from the well-known reactions (H2 production, N2 fixation, and CO2 conversion), various novel reactions are successfully catalyzed by single-atom photocatalysts possessing high efficiency, selectivity, and stability. In this contribution, we summarize and discuss the design and fabrication of single-atom photocatalysts for three different kinds of emerging reactions (i.e., reduction reactions, oxidation reactions, as well as redox reactions) to generate desirable chemicals and/or fuels. The relationships between the composition/structure of single-atom photocatalysts and their activity/selectivity/stability are explained in detail. Additionally, the insightful reaction mechanisms of single-atom photocatalysts are also introduced. Finally, we propose the possible opportunities in this area for the design and fabrication of brand-new high-performance single-atom photocatalysts.

1The causative agent of the coronavirus disease 2019 (COVID-19) pandemic, severe 2 acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is steadily mutating during continuous 3 transmission among humans. Such mutations can occur in the spike (S) protein that binds to the 4 angiotensin-converting enzyme-2 (ACE2) receptor and is cleaved by transmembrane protease 5 serine 2 (TMPRSS2). However, whether S mutations affect SARS-CoV-2 infectivity remains 6 unknown. Here, we show that naturally occurring S mutations can reduce or enhance cell entry 7 via ACE2 and TMPRSS2. A SARS-CoV-2 S-pseudotyped lentivirus exhibits substantially lower 8 entry than SARS-CoV S. Among S variants, the D614G mutant shows the highest viral entry, as 9 supported by structural observations. Nevertheless, the D614G mutant remains susceptible to 10 neutralization by antisera against prototypic viruses. Taken together, these data indicate that the 11 D614G mutation enhances viral infectivity while maintaining neutralization susceptibility. 12 13 3