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The accumulation of manganese ions is crucial for scavenging reactive oxygen species and protecting the proteome of Deinococcus radiodurans (Dr). However, metal homeostasis still needs to be tightly regulated to avoid toxicity. DR2539, a dimeric transcription regulator, plays a key role in Dr manganese homeostasis. Despite comprising three well-conserved domains - a DNA-binding domain, a dimerisation domain, and an ancillary domain - the mechanisms underlying both, metal ion activation and DNA recognition remain elusive. In this study, we present biophysical analyses and the structure of the dimerisation and DNA-binding domains of DR2539 in its holo-form and in complex with the 21 base pair pseudo-palindromic repeat of the dr1709 promoter region, shedding light on these activation and recognition mechanisms. The dimer presents eight manganese binding sites that induce structural conformations essential for DNA binding. The analysis of the protein-DNA interfaces elucidates the significance of Tyr59 and helix α3 sequence in the interaction with the DNA. Finally, the structure in solution as determined by small-angle X-ray scattering experiments and supported by AlphaFold modeling provides a model illustrating the conformational changes induced upon metal binding.
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http://dx.doi.org/10.1111/febs.17140 | DOI Listing |
Inorg Chem
September 2025
State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002, P. R. China.
The photocatalytic reduction of carbon dioxide (CO) to chemicals holds significant importance for mitigating the current energy crisis. Rational design of catalytic centers within well-defined structures can effectively enhance the reaction activity and selectivity. In this study, we constructed interrupted zeolitic boron imidazolate frameworks (BIFs) featuring unsaturated coordination at the central Co ion.
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September 2025
Key Laboratory of Electrochemical Power Sources of Hubei Province, College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, 430072, China.
Hybrid artificial layer based on inorganic/polymer composite endows superior toughness and mechanical strength, which can achieve high stability of lithium metal anode. However, the large particle size and uneven distribution of inorganic fillers hinder the uniform flow of lithium ions across the membrane, making it difficult to achieve smooth lithium metal deposition/stripping. In this work, a chemical lithiation-induced defluorination strategy is proposed to engineer poly(vinylidene difluoride) (PVDF)-based artificial layers, enabling in situ incorporation of highly dispersed LiF nanofiller within the polymer matrix and precise control over the LiF content.
View Article and Find Full Text PDFJ Agric Food Chem
September 2025
Key Laboratory of Geriatric Nutrition and Health, Beijing Technology and Business University, Haidian 100080, China.
Metal ions play a vital role in the health of the modern human body, but deficiencies in mineral elements have created health risks worldwide. However, mineral supplements currently available on the market are very limited due to poor solubility, low bioavailability, and the possibility of adverse effects on the gastrointestinal tract. In contrast, protein-derived metal-chelating peptides have received a lot of attention because of their stability, safety, and very high bioavailability.
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September 2025
Department of Chemistry, Jadavpur University, Kolkata, 700032, India.
The design of a rare combination of interpenetrated and catenated 3D+2D→3D MOF {[Cd(dim)(dht)(HO)](Sol)} (1), with a unique network and extreme pH stability, has been developed for exceptional ionic conduction across a wide range of temperature and humidity conditions. The bare pore derivative of 1 (1') features remarkable structural flexibility and large pores accessible to encapsulate molecules such as NH, HCl, and KOH, enabling it to function as an efficient conductor for both proton and hydroxide ions. 1' demonstrates substantial thermal-influenced proton conductivity of 4.
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September 2025
School of Energy and Chemical Engineering, UNIST, Ulsan, 44919, South Korea.
All-solid-state batteries (ASSBs), equipped with highly ion-conductive sulfide solid electrolytes and utilizing lithium plating/stripping as anode electrochemistry, suffer from 1) chemical vulnerability of the electrolytes with lithium and 2) physical growth of lithium to penetrate the electrolytes. By employing an ordered mesoporous graphitic carbon (OMGC) framework between a sulfide electrolyte layer and a copper current collector in ASSB, the concerns by are addressed 1) minimizing the chemically vulnerable interface (CVI) between electric conductor and solid electrolyte, and 2) allowing lithium ingrowth toward the porous structure via Coble creep, a diffusional deformation mechanism of lithium metal along the lithium-carbon interface. The void volume of the framework is fully filled with lithium metal, despite ionic pathways not being provided separately, even without additional lithiophiles, when an enough amount of lithium is allowed to be plated.
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