Aggregation-induced emission (AIE)-active fluorescent probes with multiple binding sites toward ATP sensing and live cell imaging

2017 ◽  
Vol 5 (43) ◽  
pp. 8525-8531 ◽  
Author(s):  
Hengchang Ma ◽  
Manyi Yang ◽  
Caili Zhang ◽  
Yucheng Ma ◽  
Yanfang Qin ◽  
...  
Keyword(s):  
Boric Acid ◽  
Fluorescent Probes ◽  
Binding Sites ◽  
Live Cell Imaging ◽  
Cell Imaging ◽  
Cell Organelles ◽  
Aggregation Induced Emission ◽  
Multiple Binding Sites ◽  
Multiple Binding ◽  
Atp Sensing

Herein, we report a set of novel AIE-active fluorescent probes containing pyridiniums and boric acid groups with the applications of ATP recognition and specific tracking of different cell organelles.

A systematic series of fluorescence chemosensors with multiple binding sites for Hg(ii) based on pyrenyl-functionalized cyclotriphosphazenes and their application in live cell imaging

2018 ◽  
Vol 42 (17) ◽  
pp. 14219-14228 ◽  
Author(s):  
Süreyya Oğuz Tümay ◽  
Aylin Uslu ◽  
Hüsniye Ardıç Alidağı ◽  
Hasan Hüseyin Kazan ◽  
Cansu Bayraktar ◽  
...  
Keyword(s):  
Metal Ions ◽  
Binding Sites ◽  
Live Cell Imaging ◽  
Cell Imaging ◽  
Live Cell ◽  
Multiple Binding Sites ◽  
Multiple Binding

A systematic series of fluorescence chemosensors based on cyclotriphosphazene derivatives were designed, synthesized, and evaluated for their sensing behaviors toward metal ions.

scholarly journals Fluorescent Probes with Multiple Binding Sites for the Discrimination of Cys, Hcy, and GSH

2017 ◽  
Vol 56 (43) ◽  
pp. 13188-13198 ◽  
Author(s):  
Cai-Xia Yin ◽  
Kang-Ming Xiong ◽  
Fang-Jun Huo ◽  
James C. Salamanca ◽  
Robert M. Strongin
Keyword(s):  
Fluorescent Probes ◽  
Binding Sites ◽  
Multiple Binding Sites ◽  
Multiple Binding

NMDAR PAMs: Multiple Chemotypes for Multiple Binding Sites

2019 ◽  
Vol 19 (24) ◽  
pp. 2239-2253 ◽  
Author(s):  
Paul J. Goldsmith
Keyword(s):  
Binding Sites ◽  
Receptor Activation ◽  
Research Area ◽  
Allosteric Modulators ◽  
Nonselective Cation Channels ◽  
Multiple Binding Sites ◽  
Multiple Binding ◽  
Excitatory Neurotransmission ◽  
Psychiatric Conditions ◽  
High Level

The N-methyl-D-aspartate receptor (NMDAR) is a member of the ionotropic glutamate receptor (iGluR) family that plays a crucial role in brain signalling and development. NMDARs are nonselective cation channels that are involved with the propagation of excitatory neurotransmission signals with important effects on synaptic plasticity. NMDARs are functionally and structurally complex receptors, they exist as a family of subtypes each with its own unique pharmacological properties. Their implication in a variety of neurological and psychiatric conditions means they have been a focus of research for many decades. Disruption of NMDAR-related signalling is known to adversely affect higherorder cognitive functions (e.g. learning and memory) and the search for molecules that can recover (or even enhance) receptor output is a current strategy for CNS drug discovery. A number of positive allosteric modulators (PAMs) that specifically attempt to overcome NMDAR hypofunction have been discovered. They include various chemotypes that have been found to bind to several different binding sites within the receptor. The heterogeneity of chemotype, binding site and NMDAR subtype provide a broad landscape of ongoing opportunities to uncover new features of NMDAR pharmacology. Research on NMDARs continues to provide novel mechanistic insights into receptor activation and this review will provide a high-level overview of the research area and discuss the various chemical classes of PAMs discovered so far.

Effects of Multiple Binding Sites on Studies of Hydrogen Bonding between Nitroxide Radicals and Solvent Molecules

1993 ◽  
Vol 58 (1) ◽  
pp. 47-52 ◽  
Author(s):  
Imad Al-Bala'a ◽  
Richard D. Bates
Keyword(s):  
Hydrogen Bonding ◽  
Magnetic Resonance ◽  
Binding Site ◽  
Binding Sites ◽  
Hyperfine Coupling Constant ◽  
Hydrogen Donor ◽  
Complex Formation Constants ◽  
Multiple Binding Sites ◽  
Multiple Binding ◽  
Solvent Molecules

The role of more than one binding site on a nitroxide free radical in magnetic resonance determinations of the properties of the complex formed with a hydrogen donor is examined. The expression that relates observed hyperfine couplings in EPR spectra to complex formation constants and concentrations of each species in solution becomes much more complex when multiple binding sites are present, but reduces to a simpler form when binding at the two sites occurs independently and the binding at the non-nitroxide site does not produce significant differences in the hyperfine coupling constant in the complexed radical. Effects on studies of hydrogen bonding between multiple binding site nitroxides and hydrogen donor solvent molecules by other magnetic resonance methods are potentially more extreme.

Creating BHb-imprinted magnetic nanoparticles with multiple binding sites

The Analyst ◽  
2017 ◽  
Vol 142 (2) ◽  
pp. 302-309 ◽  
Author(s):  
Yanxia Li ◽  
Yiting Chen ◽  
Lu Huang ◽  
BenYong Lou ◽  
Guonan Chen
Keyword(s):  
Magnetic Nanoparticles ◽  
Binding Sites ◽  
Multifunctional Nanoparticles ◽  
Multiple Binding Sites ◽  
Multiple Binding

A kind of protein imprinted over magnetic Fe3O4@Au multifunctional nanoparticles (NPs) with multiple binding sites was synthesized and investigated.

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