نتایج جستجو برای: affinity ligands

تعداد نتایج: 180734  

Journal: :Chemistry: A European Journal 2021

Targeting the interface between DNA quadruplex and duplex regions by small molecules holds significant promise in both therapeutics nanotechnology. Herein, a new pharmacophore is reported, which selectively binds with high affinity to quadruplex–duplex junctions, while presenting poorer for G-quadruplex or alone. Ligands complying reported exhibit selectivity including one observed HIV-1 LTR-II...

2016
M. P. TORASKAR

Objective: The present study was carried out to study the binding interactions of different N’-(substituted phenyl sulfonyl)-pyridine-2carbohydrazide derivatives and N’-(substituted phenyl sulfonyl)-thiophene-2-carbohydrazide derivatives which were synthesized by senior students from research laboratory, with objective to explore the suitability of selected ligands for their binding affinity fo...

2009
Dong Long Yuguang Mu Daiwen Yang

The mechanisms of how ligands enter and leave the binding cavity of fatty acid binding proteins (FABPs) have been a puzzling question over decades. Liver fatty acid binding protein (LFABP) is a unique family member which accommodates two molecules of fatty acids in its cavity and exhibits the capability of interacting with a variety of ligands with different chemical structures and properties. ...

2011
Jillian G. Baker Luke A. Adams Karolina Salchow Shailesh N. Mistry Richard J. Middleton Stephen J. Hill Barrie Kellam

The growing practice of exploiting noninvasive fluorescence-based techniques to study G protein-coupled receptor pharmacology at the single cell and single molecule level demands the availability of high-quality fluorescent ligands. To this end, this study evaluated a new series of red-emitting ligands for the human β-adrenoceptor family. Upon the basis of the orthosteric ligands propranolol, a...

Journal: :Journal of virology 2012
Elena Lorente Susana Infantes Eilon Barnea Ilan Beer Ruth García Fátima Lasala Mercedes Jiménez Carlos Vilches François A Lemonnier Arie Admon Daniel López

The transporter associated with antigen processing (TAP) delivers the viral proteolytic products generated by the proteasome in the cytosol to the endoplasmic reticulum lumen that are subsequently recognized by cytotoxic T lymphocytes (CTLs). However, several viral epitopes have been identified in TAP-deficient models. Using mass spectrometry to analyze complex human leukocyte antigen (HLA)-bou...

Journal: :The Journal of biological chemistry 1998
C S Breivogel D E Selley S R Childers

The relationship between GDP and cannabinoid-stimulated [35S]guanosine-5'-O-(3-thiotriphosphate) ([35S]GTPgammaS) binding was investigated in rat cerebellar membranes. Kinetic analyses showed that [35S]GTPgammaS binding reached steady-state levels and that the association rate was increased by the agonist WIN 55212-2 proportional to the concentration of GDP. Dissociation of [35S]GTPgammaS occur...

Journal: :Journal of Immunology 2021

Abstract Germinal center reactions are established during a thymus-dependent immune response. (GC) B cells rapidly proliferating and undergo somatic hypermutation in Ab genes. This results the production of high-affinity Abs establishment long-lived memory cells. GC show lower BCR-induced signaling when compared with naive cells, but functional relevance is not clear. CD22 member Siglec family ...

Journal: :The Journal of biological chemistry 2010
Haina Qin Roberta Noberini Xuelu Huan Jiahai Shi Elena B Pasquale Jianxing Song

EphA and EphB receptors preferentially bind ephrin-A and ephrin-B ligands, respectively, but EphA4 is exceptional for its ability to bind all ephrins. Here, we report the crystal structure of the EphA4 ligand-binding domain in complex with ephrin-B2, which represents the first structure of an EphA-ephrin-B interclass complex. A loose fit of the ephrin-B2 G-H loop in the EphA4 ligand-binding cha...

Journal: :The Journal of biological chemistry 2015
Francieli Colussi Trine H Sørensen Kadri Alasepp Jeppe Kari Nicolaj Cruys-Bagger Michael S Windahl Johan P Olsen Kim Borch Peter Westh

Cellobiohydrolases break down cellulose sequentially by sliding along the crystal surface with a single cellulose strand threaded through the catalytic tunnel of the enzyme. This so-called processive mechanism relies on a complex pattern of enzyme-substrate interactions, which need to be addressed in molecular descriptions of processivity and its driving forces. Here, we have used titration cal...

Journal: :Chemistry 2016
Philipp Rohse Valentin Wittmann

Multivalent carbohydrate-protein interactions are frequently involved in essential biological recognition processes. Accordingly, multivalency is often also exploited for the design of high-affinity lectin ligands aimed at the inhibition of such processes. In a previous study (D. Schwefel et al., J. Am. Chem. Soc. 2010, 132, 8704-8719) we identified a tetravalent cyclopeptide-based ligand with ...

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