The effective distribution of affinities (Conditional Affinity Spectrum, CAS) seen by a metal ion binding to a humic substance under natural water conditions is derived and discussed within the NICA-Donnan model. Analytical expressions for the average affinity of these distributions in general multi-ion mixtures are reported here for the first time. These expressions enable a simple evaluation of the effect of all interfering cations on the affinity distribution of a given one. We illustrate this methodology by plotting the affinity spectra of a generic fulvic acid for 14 different cations in the presence of major inorganic ions and trace metals at pH and concentration values representative of a river water. The distribution of occupied sites and their average affinity at the typical freshwater conditions are also reported for each ion. The CAS allows usto distinguish three groups of cations: (a) Al, H, Pb, Hg, and Cr, which are preferentially bound to the phenolic sites of the fulvic ligand; (b) Ca, Mg, Cd, Fe(II), and Mn, which display a greater effective affinity for carboxylic sites, in contrast to what would be expected from their individual complexation parameters; and (c) Fe(III), Cu, Zn, and Ni, for which phenolic and carboxylic distributions are overlapped.
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http://dx.doi.org/10.1021/es803006p | DOI Listing |
Eur J Nucl Med Mol Imaging
December 2024
Department of Nuclear Medicine, Peking University First Hospital, No. 8 Xishiku Str., Xicheng Dist, Beijing, 100034, China.
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View Article and Find Full Text PDFJ Am Chem Soc
December 2024
Department of Chemical Sciences and Center for Advanced Functional Materials, Indian Institute of Science Education and Research (IISER) Kolkata, Mohanpur 741246, West Bengal, India.
Triple-negative breast cancer (TNBC) poses significant treatment challenges due to its high metastasis, heterogeneity, and poor biomarker expression. The N-terminus of an octapeptide NAPVSIPQ () was covalently coupled to a carboxylic acid derivative of Ru(2,2'-bipy) () to synthesize an N-stapled short peptide-Rubpy conjugate (). This photosensitizer (PS) was utilized to treat TNBC through microtubule (MT) targeted chemotherapy and photodynamic therapy (PDT).
View Article and Find Full Text PDFBiochim Biophys Acta Gen Subj
December 2024
Department of Biochemistry, Faculty of Life Sciences, Aligarh Muslim University, Aligarh 202002, India. Electronic address:
The interaction of drugs with DNA is crucial for understanding their mechanism of action, particularly in the context of gene expression regulation. Erdafitinib (EDB), a pan-FGFR (fibroblast growth factor receptor) inhibitor approved by the FDA, is a potent anticancer agent used primarily in the treatment of urothelial carcinoma. In this study, the binding interaction between EDB and calf thymus DNA (ctDNA) was assessed using molecular docking, UV-absorption spectroscopy, fluorescence spectroscopy, and circular dichroism (CD) spectroscopy.
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Department of Obstetrics, Key Laboratory of Birth Defects and Related Disease of Women and Children of MOE, State Key Laboratory of Biotherapy, West China Second Hospital, Sichuan University, Chengdu 610041, China; NHC key Laboratory of Chronobiology, Sichuan University, Chengdu 610041, China. Electronic address:
Malaria caused by Plasmodium infection poses a serious hazard to human health. P. falciparum equilibrative nucleoside transporter 1 (PfENT1), which mediates nucleoside uptake, is essential for the growth and proliferation of Plasmodium parasites, suggesting that PfENT1 is a potential antimalarial target.
View Article and Find Full Text PDFJ Inorg Biochem
December 2024
Faculty of Chemistry (UPV/EHU), Manuel Lardizabal 3, Donostia-San Sebastian 20018, Spain; DIPC, Manuel Lardizabal 4, Donostia-San Sebastian 20018, Spain. Electronic address:
Mimosine, a non-essential amino acid derived from plants, has a strong affinity for binding divalent and trivalent metal cations, including Zn, Ni, Fe, and Al. This ability endows mimosine with significant antimicrobial and anti-cancer properties, making it a promising candidate for therapeutic applications. Previous research has demonstrated the effectiveness of mimosine-containing peptides as metal chelators, offering a safer alternative to conventional chelation agents.
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