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Rotavirus double-layered particles (DLPs) are studied in the gas phase with a high-resolution differential mobility analyzer (DMA). DLPs were transferred to 10 mM aqueous ammonium acetate, electrosprayed into the gas phase, converted into primarily singly charged particles, and DMA-analyzed. Up to seven slightly different conformations were resolved, whose apparently random, fast (minutes), and reversible interconversions were followed in real time. They sometimes evolved into just two distinct structures, with periods of one dominating over the other and vice versa. Differences between the DLP structures in solution and in the gas phase are clearly revealed by the smaller DLP diameter found here (60 versus 70 nm). Nevertheless, we argue that the multiple gas-phase conformers observed originate in as many conformations pre-existing in solution. We further hypothesize that these conformers correspond to incomplete DLPs having lost some of the VP6 trimer quintets surrounding each of the 12 5-fold axes. Instances of this peculiar loss have been previously documented by cryoelectron microscopy for the rotavirus Wa strain, as well as via charge detection mass spectrometry for five other rotavirus strains included in the RotaTec vaccine. Evidence of this loss systematically found for all 7 rotavirus types so far studied in aqueous ammonium acetate may be a special feature of this electrolyte.
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http://dx.doi.org/10.1021/acs.analchem.3c01994 | DOI Listing |
J Am Chem Soc
September 2025
National Engineering Research Center of Lower-Carbon Catalysis Technology, Dalian National Laboratory for Clean Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
Zeolite-confined Rh-based catalysts have emerged as promising heterogeneous candidates for olefin hydroformylation. However, they face challenges of reactant- and product-induced Rh leaching and aggregation. Herein, zeolite framework-anchored Rh-(O-Zn) sites were designed and are shown to have remarkable activity and stability for gas-phase ethylene hydroformylation.
View Article and Find Full Text PDFPhys Rev Lett
August 2025
Linac Coherent Light Source, SLAC National Accelerator Laboratory, Menlo Park, California 94025, USA.
We have observed the signatures of valence electron rearrangement in photoexcited ammonia using ultrafast hard x-ray scattering. Time-resolved x-ray scattering is a powerful tool for imaging structural dynamics in molecules because of the strong scattering from the core electrons localized near each nucleus. Such core-electron contributions generally dominate the differential scattering signal, masking any signatures of rearrangement in the chemically important valence electrons.
View Article and Find Full Text PDFSoft Robot
September 2025
Bioinspired Soft Robotics Laboratory, Istituto Italiano di Tecnologia, Genoa, Italy.
Animal diaphragm-lung systems are soft organs that generate a controllable vacuum. Elephants, as rare land animals, can manipulate all three states of matter using their lung-generated vacuum. In soft robotics, however, current vacuum generation relies on rigid components, and no single soft device effectively handles all states of matter.
View Article and Find Full Text PDFPhys Chem Chem Phys
September 2025
Department of Chemistry, University of Victoria, Victoria, BC V8W 2Y2, Canada.
The adsorption of amino acids on coinage metal surfaces is of interest for a range of biological applications. Central to advancing these applications is understanding the structure of the adsorbed molecules and the state they are present in. Cysteine, the focus of this work, has been studied extensively, both experimentally and theoretically.
View Article and Find Full Text PDFPhys Chem Chem Phys
September 2025
School of Chemical Sciences, Indian Association for the Cultivation of Science, 2A Raja S C Mullick Road, Jadavpur, Kolkata 700032, India.
This work presents a gas-phase experimental study on the reduction of NO (nitrogen dioxide) to HONO (nitrous acid) by two atmospherically significant volatile organic compounds (VOCs), namely, glycolaldehyde (Gla) and hydroxyacetone (HAc), under a simulated tropospheric condition. FTIR spectroscopic probing reveals that HONO is the only gaseous reduced product of NO in each reaction. The measured data indicate that the reactions in both cases occur in a 2 : 1 stoichiometry with respect to NO and Gla/HAc.
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