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Carbohydrate-binding proteins from pathogenic bacteria and fungi have been shown to be implicated in various pathological processes, where they interact with glycans present on the surface of the host cells. These interactions are part of the initial processes of infection of the host and are very important to study at the atomic level. Here, we report the room temperature neutron structures of PLL lectin from Photorhabdus laumondii in its apo form and in complex with deuterated L-fucose, which is, to our knowledge, the first neutron structure of a carbohydrate-binding protein in complex with a fully deuterated carbohydrate ligand. A detailed structural analysis of the lectin-carbohydrate interactions provides information on the hydrogen bond network, the role of water molecules, and the extent of the CH-π stacking interactions between fucose and the aromatic amino acids in the binding site.
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http://dx.doi.org/10.1016/j.str.2021.03.003 | DOI Listing |
ACS Omega
September 2025
Chongqing Key Laboratory of Green Synthesis and Applications, College of Chemistry, Chongqing Normal University, Chongqing 401331, China.
Nanozymes, which possess inherent catalytic properties that are akin to those of natural enzymes, have emerged as promising candidates for biomedical innovation. In this work, we successfully synthesize a Co Cu S nanoflower by the solvothermal and soaking method. Fortunately, through cobalt doping and microstructure design, its morphological structure and active sites have been optimized and adjusted, thus bestowing the Co Cu S nanoflower enhanced peroxidase-mimetic activity.
View Article and Find Full Text PDFFEBS J
September 2025
Neutron Scattering Division, Oak Ridge National Laboratory, USA.
Serine hydroxymethyltransferase (SHMT) is a critical enzyme in the one-carbon (1C) metabolism pathway catalyzing the reversible conversion of L-Ser into Gly and concurrent transfer of 1C unit to tetrahydrofolate (THF) to give 5,10-methylene-THF (5,10-MTHF), which is used in the downstream syntheses of biomolecules critical for cell proliferation. The cellular 1C metabolism is hijacked by many cancer types to support cancer cell proliferation, making SHMT a promising target for the design and development of novel small-molecule antimetabolite chemotherapies. To advance structure-assisted drug design, knowledge of SHMT catalysis is crucial, but can only be fully realized when the atomic details of each reaction step governed by the acid-base catalysis are elucidated by visualizing active site hydrogen atoms.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
School of Chemical Engineering and Technology, Hebei University of Technology, XiPing Dao 5340, Beichen District, Tianjin 300401, P. R. China.
Perfluorooctanoic acid (PFOA) is a persistent organic pollutant with a global presence in water, air, and soil resources. Herein, a water-stable amine-functionalized lanthanide metal-organic framework () is utilized for ratiometric luminescence detection of PFOA. In the presence of PFOA, there is an increase in the emission intensity of the organic ligand, while the characteristic luminescence intensity of Eu ions decreases, accompanied by a distinct emission color change from red to blue.
View Article and Find Full Text PDFInt J Cosmet Sci
September 2025
Centre of High Field NMR Spectroscopy and Imaging, Nanyang Technological University, Singapore, Singapore.
Objective: Small molecules, like panthenol have been shown to penetrate hair. However, their interactions with the protein structures of hair have not been well studied. In this study, the penetration of panthenol into protein structures of hair was confirmed, and NMR methods were utilized to understand the protein-panthenol interaction.
View Article and Find Full Text PDFMedicine (Baltimore)
August 2025
Clinical Laboratory, Sichuan Province Orthopedic Hospital, Chengdu, Sichuan, China.
This study aims to explore the mechanism of artemisinin in treating osteoarthritis (OA) through bioinformatics and network pharmacology. The targets of artemisinin were obtained from databases such as TCMSP, and the disease targets of OA were screened from OMIM, TTD, DisGeNET, and GEO databases. The predicted targets of artemisinin were intersected with OA disease targets to obtain drug-disease common targets, which were visualized using a Venn diagram.
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