Dependence of avidity on linker length for a bivalent ligand-bivalent receptor model system.
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In situ click chemistry: from small molecule discovery to synthetic antibodiesStructural Basis for Kinesin-1:Cargo RecognitionDesigning cell-targeted therapeutic proteins reveals the interplay between domain connectivity and cell bindingA general strategy to endow natural fusion-protein-derived peptides with potent antiviral activityPolybivalency and disordered proteins in ordering macromolecular assemblies.Development and validation of an UPLC-MS/MS method for the quantification of ethoxzolamide in blood, brain tissue, and bioequivalent buffers: applications to absorption, brain distribution, and pharmacokinetic studies.An efficient strategy to enhance binding affinity and specificity of a known isozyme inhibitorStereodivergent synthesis of right- and left-handed iminoxylitol heterodimers and monomers. Study of their impact on β-glucocerebrosidase activity.In Vivo Efficacy of Measles Virus Fusion Protein-Derived Peptides Is Modulated by the Properties of Self-Assembly and Membrane Residence.Multivalent inhibitors for carbohydrate-processing enzymes: beyond the "lock-and-key" concept.Cholesterol-conjugated peptide antivirals: a path to a rapid response to emerging viral diseases.Emerging trends in enzyme inhibition by multivalent nanoconstructs.Fluorescent Silica Nanoparticles with Multivalent Inhibitory Effects towards Carbonic Anhydrases.Designing nanomolar antagonists of DC-SIGN-mediated HIV infection: ligand presentation using molecular rods.Development of a high affinity, non-covalent biologic to add functionality to Fabs.Mix and match backbones for the formation of H-bonded duplexes.Influence of length and flexibility of spacers on the binding affinity of divalent ligands.A general model for predicting the binding affinity of reversibly and irreversibly dimerized ligands.Multimeric xanthates as carbonic anhydrase inhibitors.Mechanistic Insight into Heptosyltransferase Inhibition by using Kdo Multivalent Glycoclusters.Pyruvate-Kinase-Coupled Glycosyltransferase Assays: Limitations, Struggles and Problem Resolution.Deconstructing behavioral neuropharmacology with cellular specificity.Optimizing divalent inhibitors of Pseudomonas aeruginosa lectin LecA by using a rigid spacer.Cooperative duplex formation by synthetic H-bonding oligomers.Reversible blocking of antibodies using bivalent peptide–DNA conjugates allows protease-activatable targeting
P2860
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P2860
Dependence of avidity on linker length for a bivalent ligand-bivalent receptor model system.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Dependence of avidity on linke ...... ivalent receptor model system.
@en
type
label
Dependence of avidity on linke ...... ivalent receptor model system.
@en
prefLabel
Dependence of avidity on linke ...... ivalent receptor model system.
@en
P2093
P2860
P356
P1476
Dependence of avidity on linke ...... ivalent receptor model system.
@en
P2093
Başar Bilgiçer
Demetri T Moustakas
Eric T Mack
George M Whitesides
Phillip W Snyder
Raquel Perez-Castillejos
P2860
P304
P356
10.1021/JA2073033
P407
P577
2011-12-21T00:00:00Z