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Albumin molecules are extensively used as biocompatible coatings, and poly(ethylene glycol) (PEG) materials are widely used for antifouling. PEG materials have excellent antifouling property because of their strong surface hydration. Our previous research indicates that hydration at the PEG/bovine serum albumin solution interface is stronger than that at the PEG/water interface. This research shows that this observation is general for different types of albumin molecules. Different albumins including bovine, porcine, rat, rabbit, and sheep serum albumins were studied in this research. It was found that the hydration at the PEG methacrylate (pOEGMA)/albumin solution interface is always stronger than that at the pOEGMA/water interface. Here, we define "strong interfacial hydration" as "ordered strongly hydrogen-bonded interfacial water". We believe that such a strong hydration is because of the strong hydration on the albumin surface, leading to its biocompatible property. All of the albumin molecules demonstrated stronger hydration on the pOEGMA surface compared to other protein molecules such as lysozyme and fibrinogen. The strong hydration on albumin molecules is related to the high surface coverage of glutamic acid and lysine with similar amounts.
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http://dx.doi.org/10.1021/acs.langmuir.9b03680 | DOI Listing |
Proc Natl Acad Sci U S A
September 2025
Department of Materials Science and Engineering, City University of Hong Kong, Kowloon, Hong Kong 999077, China.
Solid-state electrolytes (SSEs) are being extensively researched as replacements for liquid electrolytes in future batteries. Despite significant advancements, there are still challenges in using SSEs, particularly in extreme conditions. This study presents a hydrated metal-organic ionic cocrystal (HMIC) solid-state ion conductor with a solvent-assisted ion transport mechanism suitable for extreme operating conditions.
View Article and Find Full Text PDFACS Omega
September 2025
Australian Nuclear Science and Technology Organisation, Locked Bag 2001, Kirrawee DC, NSW 2232, Australia.
We report the hydrothermal syntheses and structural and spectroscopic characterization of two new uranium oxide hydrate frameworks (UOHFs) with either Pr or Nd ions, Pr(HO)[(UO)UO(OH)] () or Nd(HO)[(UO)UO(OH)] (). Both UOHFs crystallize in the orthorhombic 222 space group and display needle crystal morphologies. Their crystal structures are composed of β-UO-type layers connected by double uranium polyhedra to form the frameworks, with disordered Pr/Nd ions within the framework channels, as revealed by synchrotron single-crystal XRD.
View Article and Find Full Text PDFSerpentinites, hydrated ultramafic rocks that produce [hyper]alkaline, reducing, H2-rich groundwaters, host subsurface microbial ecosystems. Though in the presence of enormous reducing power, life in serpentinizing systems is limited by oxidant and carbon availability. The forms of carbon that support the serpentinite-hosted microbiome, and their rates of biological assimilation, remain poorly understood.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
Department of Materials Science and Engineering, University of Washington, Seattle, WA 98195, USA. Electronic address:
Pre-intercalation has emerged as a highly effective strategy to enhance structural integrity and ion transport kinetics in cathodes for aqueous Zn-ion batteries. Here, we report a zinc-ion pre-intercalated hydrate vanadium oxide cathode, in which the initial insertion of Zn induces a significant expansion of the interplanar spacing, followed by contraction at higher Zn concentrations owing to strong electrostatic interactions with the VO framework. Such competing expansion and contraction of interplanar spacing enhances the overall electrochemical properties.
View Article and Find Full Text PDFJ Phys Chem B
September 2025
Hubei Key Laboratory of Drug Synthesis and Optimization, Jingchu University of Technology, Jingmen, Hubei 448000, China.
Phosphoric acid (PA) retention is essential for the efficient and stable operation of PA-doped proton exchange membranes (PEMs) in fuel cells. The strength of the interactions between polymer functional groups and PA is a key determinant of PA retention. In this work, we systematically investigate the interactions between zwitterionic sulfobetaines (SBs) with varying carbon spacer lengths (CSLs) and PA under both anhydrous and hydrated conditions using density functional theory calculations and molecular dynamics (MD) simulations.
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