By an analysis of PDB crystal structures, the mean conformations of protein strands bound in serine protease active sites are shown to contain extensively aligned atomic orbitals. The active-serine-bearing segment of each enzyme (subtilisin BPN' and beta-trypsin) also contains such alignments. The participating orbitals are almost identical in each system. All of the alignments converge on the targeted linkage. They suggest that a kind of through-strand polarizability is being optimized by evolution, presumably due to corresponding benefits in proteolysis rate. Such polarizability would help to explain the high values of kcat seen for long oligopeptide substrates. The idea predicts long substrates to be relatively reactive even under non-enzymatic conditions, which in fact they are.
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http://dx.doi.org/10.1016/j.bmc.2004.02.044 | DOI Listing |
Angew Chem Int Ed Engl
January 2025
Nanjing University, School of Chemistry and Chemical Engineering, Nanjing University, 163 Xianlin Avenue, 210023, Nanjing, CHINA.
Ultra-narrowband and highly modifiable multiple resonance thermally activated delayed fluorescence (MR-TADF) materials are crucial for realizing high-performance wide-color-gamut display applications. Despite progress, most MR-TADF emitters remain confined to blue and green wavelengths, with difficulties extending into longer wavelengths without significant spectral broadening, which compromises color purity in full-color organic light-emitting diode (OLED) displays. In this work, we present a novel tetraazacyclophane-based architecture embedding dual boron atoms to remarkedly enhance intramolecular charge transfer through the strategic positioning of boron and nitrogen atoms.
View Article and Find Full Text PDFChemistry
December 2024
Technological University Dublin, Institute of Polymers, Kevin Street, Dublin 8, Dublin, IRELAND.
Donor-acceptor BODIPY dyads, functionalized at the 2 and 6 positions with benzyl ester (BDP-DE) or carboxylic acid (BDP-DA) groups, were synthesized and characterized for their optoelectronic properties. The introduction of carbonyl groups increased the reduction potential of the BODIPY core by 0.15-0.
View Article and Find Full Text PDFRSC Adv
December 2024
Laboratory of Computational Chemistry and Modelling (LCCM), Quy Nhon University 170 An Duong Vuong Street Quy Nhon City 590000 Vietnam
Forty-eight stable structures of complexes formed between XCHZ and RCZOH (with X = H, F; R = H, F, Cl, Br, CH, NH; Z = O, S, Se, Te) were comprehensively investigated. It was found that the HZ-RZ complexes were more stable than the FZ-RZ ones, and their stability tendency decreased in the following order of Z: O > S > Se > Te. A predominant role of the electrostatic component was observed in XO-RO, while an outstanding contribution of the induction term was estimated in XS-RS, XSe-RSe, and XTe-RTe.
View Article and Find Full Text PDFChemistry
December 2024
University of Trieste, Department of Chemical and Pharmaceutical Sciences, Via Licio Giorgieri, 1, 34127, Trieste, ITALY.
In this work, we elucidate the electronic charge redistributions that occur within the cyanuric acid (CA) and melamine (M) molecules upon formation of the triple H-bond between the imide group of CA and the diaminopyridine group of M. To achieve this, we investigated 2D H-bonded assemblies of M, CA and CA*M grown on the Au(111) surface, using X-ray photoemission (XPS) and near edge X-ray absorption fine structure (NEXAFS) spectroscopies. Compared to the homomolecular networks, the spectra of the mixed sample reveal core level shifts in opposite directions for CA and M, indicating a nearly complementary charge accumulation on the CA molecule and a charge depletion on the M molecule.
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