Recent use of hetero-dimerization to improve the affinity of peptide ligands has made peptides an attractive alternative to small molecules and proteins. Using this strategy, we have developed peptides with affinities comparable to antibodies and specificities often better than small molecules or antibodies. These peptides can be used as a delivery vehicle for drugs or diagnostics, especially in the case of tumor targeting cytotoxic drugs or targeted diagnostics. We describe here an assay to identify an ideal pair of peptides suitable for heterovalent ligands.
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http://dx.doi.org/10.1007/978-1-62703-673-3_7 | DOI Listing |
ACS Appl Mater Interfaces
January 2025
School of Chemical Engineering, University of Science and Technology Liaoning, Anshan 114051, China.
Vanadium-based materials, which offer multiple oxidation states and rich redox reactions in zinc-ion batteries (ZIBs), have gained substantial attention. However, achieving green and efficient preparation of vanadium oxides-based materials featured with a controlled content of different heterovalent vanadium remains a significant challenge. Herein, a vanadium-supramolecular flower-shaped material (VSF) with heterovalent vanadium was prepared using NHVO as vanadium metal center and hexamethylenetetramine as organic ligand in aqueous solution.
View Article and Find Full Text PDFChem Sci
September 2022
Lehrstuhl für Anorganische Koordinationschemie, Institut für Anorganische Chemie, Universität Stuttgart Pfaffenwaldring 55 70569 Stuttgart Germany.
Diamidobenzene ligands are a prominent class of redox-active ligands owing to their electron reservoir behaviour, as well as the possibility of tuning the steric and the electronic properties of such ligands through the substituents on the N-atoms of the ligands. In this contribution, we present Rh(iii) complexes with four differently substituted diamidobenzene ligands. By using a combination of crystallography, NMR spectroscopy, electrochemistry, UV-vis-NIR/EPR spectroelectrochemistry, and quantum chemical calculations we show that the substituents on the ligands have a profound influence on the bonding, donor, electrochemical and spectroscopic properties of the Rh complexes.
View Article and Find Full Text PDFSpectrochim Acta A Mol Biomol Spectrosc
October 2022
Department of Chemistry, Central University of Haryana, Mahendergarh 123031, India. Electronic address:
Bridged dinuclear metal complexes have fascinated scientists worldwide, and remarkable success has been achieved to unravel the electronic structures, structure-function relationship, coordination environments, and fine mechanistic details of the enzymes owing to the repercussion of biomimetic studies carried out on dinuclear model systems. Molecular level study of these systems integrated with spectroscopic study helps in gaining deep insights about structural and electronic aspects of natural enzymatic systems. Considering the same, here first time we report DFT study on bridged non-heme metal complexes based on N-Et-HPTB ligand system containing homovalent (MM); {[(Mn)(OCCH)(N-Et-HPTB)]; Species I), [(Fe)(OCCH)(N-Et-HPTB)]; Species II), [(Co)(OCCH)(N-Et-HPTB)]; Species III)} and heterovalent (MM): {[(Mn)(Mn)(O)(N-Et-HPTB)]; Species Ia) [(Fe)(Fe)(O)(N-Et-HPTB)]; Species IIa) and [(Co)(Co)(O)(N-Et-HPTB)]; Species IIIa)} dinuclear metal centres.
View Article and Find Full Text PDFChempluschem
December 2021
Univ. Grenoble Alpes, CNRS, DCM UMR 5250, 38000, Grenoble, France.
Click chemistry gives access to unlimited set of multivalent glycoconjugates to explore carbohydrate-protein interactions and discover high affinity ligands. In this study, we have created supramolecular systems based on a carrier protein that was grafted by Cu(I)-catalyzed azide-alkyne cycloaddition with tetravalent glycodendrons presenting αGal, βGal and/or αFuc. Binding studies of the homo- (4 a-c) and heterovalent (5) neoglycoproteins (neoGPs) with the LecA and LecB lectins from P.
View Article and Find Full Text PDFJ Phys Chem Lett
April 2021
Beijing Key Laboratory of Construction Tailorable Advanced Functional Materials and Green Applications, School of Materials Science and Engineering, Beijing Institute of Technology, Beijing 100081, P. R. China.
Doping-related point defect engineering in low-dimensional semiconductor nanostructures is important to regulate their optical and electronic properties. The substitutional or interstitial location of heterovalent dopants is critical and has not been controlled effectively yet. Herein, we carefully control the kinetics of reverse cation exchange between CuS 2D nanosheets and ligand-coordinated Cd cations to control the Cu doping sites in CdS nanosheets (NSs).
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