Results 41 to 50 of about 3,018,689 (332)

Real-time reliable determination of binding kinetics of DNA hybridization using a multi-channel graphene biosensor

open access: yesNature Communications, 2017
Reliable determination of binding kinetics and affinity of DNA hybridization and single-base mismatches plays an essential role in systems biology, personalized and precision medicine.
Shicai Xu   +10 more
semanticscholar   +1 more source

Ligand-receptor binding kinetics in drug design [PDF]

open access: yesBiomeditsinskaya Khimiya, 2020
Traditionally, the thermodynamic values of affinity are considered as the main criterion for the development of new drugs. Usually, these values for drugs are measured in vitro at steady concentrations of the receptor and ligand, which are differed from in vivo environment.
D V, Borisov, A V, Veselovsky
openaire   +2 more sources

A live cell NanoBRET binding assay allows the study of ligand-binding kinetics to the adenosine A3 receptor

open access: yesPurinergic Signalling Purinergic Signalling, 2019
There is a growing interest in understanding the binding kinetics of compounds that bind to G protein-coupled receptors prior to progressing a lead compound into clinical trials.
Mónica Bouzo-Lorenzo   +6 more
semanticscholar   +1 more source

Microtubule binding kinetics of membrane-bound kinesin-1 predicts high motor copy numbers on intracellular cargo

open access: yesProceedings of the National Academy of Sciences of the United States of America, 2019
Significance Long-distance transport of membrane-coated vesicles involves coordination of multiple motors such that at least one motor is bound to the microtubule at all times. Microtubule attachment of a membrane-bound motor comprises 2 steps: diffusing
Rui Jiang   +5 more
semanticscholar   +1 more source

Harmonic oscillator model of the insulin and IGF1 receptors’ allosteric binding and activation

open access: yesMolecular Systems Biology, 2009
The insulin and insulin‐like growth factor 1 receptors activate overlapping signalling pathways that are critical for growth, metabolism, survival and longevity.
Vladislav V Kiselyov   +3 more
doaj   +1 more source

A RAGE-Targeted Antibody-Drug Conjugate: Surface Plasmon Resonance as a Platform for Accelerating Effective ADC Design and Development

open access: yesAntibodies, 2019
Antibodies, antibody-like molecules, and therapeutics incorporating antibodies as a targeting moiety, such as antibody-drug conjugates, offer significant potential for the development of highly efficacious drugs against a wide range of disorders. Despite
Gareth D. Healey   +4 more
doaj   +1 more source

Real-time tracking of drug binding to influenza A M2 reveals a high energy barrier

open access: yesJournal of Structural Biology: X, 2023
The drug Rimantadine binds to two different sites in the M2 protein from influenza A, a peripheral site and a pore site that is the primary site of efficacy.
Kumar Tekwani Movellan   +5 more
doaj   +1 more source

Multi-scale modeling of drug binding kinetics to predict drug efficacy

open access: yesCellular and Molecular Life Sciences, 2019
Optimizing drug therapies for any disease requires a solid understanding of pharmacokinetics (the drug concentration at a given time point in different body compartments) and pharmacodynamics (the effect a drug has at a given concentration). Mathematical
F. Clarelli   +4 more
semanticscholar   +1 more source

Kinetics of calcium binding to calbindin mutants [PDF]

open access: yesEuropean Journal of Biochemistry, 1988
The kinetics of calcium dissociation from wild‐type bovine calbindin D9k (the smallest protein known with a pair of EF‐hand calcium‐binding sites) and five mutants with single amino‐acid substitutions and/or deletions has been studied by stopped‐flow fluorescence methods, using the calcium chelator Quin 2.
S, Forsén   +7 more
openaire   +2 more sources

Probe dependency in the determination of ligand binding kinetics at a prototypical G protein-coupled receptor

open access: yesScientific Reports, 2019
Drug-target binding kinetics are suggested to be important parameters for the prediction of in vivo drug-efficacy. For G protein-coupled receptors (GPCRs), the binding kinetics of ligands are typically determined using association binding experiments in ...
R. Bosma   +12 more
semanticscholar   +1 more source

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