4.6 Article

Triarylborane-Click Fluorescent Tag for Orthogonal Amino Acid Labelling, Interactions with DNA, Protein, and Cyclodextrins

Related references

Note: Only part of the references are listed.
Article Spectroscopy

Spectroscopic analysis to identify the binding site for Rifampicin on Bovine Serum Albumin

Sudhanshu Sharma et al.

Summary: This study reported the interaction of rifampicin with Bovine Serum Albumin (BSA) by monitoring the fluorescence properties of tryptophan residue in BSA. The fluorescence intensity of BSA was significantly quenched by rifampicin, specifically affecting the Trp-213 residue. Molecular docking studies confirmed the proximity of rifampicin to the Trp-213 residue in the drug-protein complex.

SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY (2022)

Article Chemistry, Multidisciplinary

Bis(phenylethynyl)arene Linkers in Tetracationic Bis-triarylborane Chromophores Control Fluorimetric and Raman Sensing of Various DNAs and RNAs

Matthias Ferger et al.

Summary: The new luminescent tetracationic bis-triarylborane DNA and RNA sensors exhibit high binding affinities, with substituted bis(2,6-dimethylphenyl-4-ethynyl)arene linkers serving as efficient dual Raman and fluorescence chromophores. The linker length and flexibility significantly affect the binding affinities, with triple bonds playing a crucial role in Raman activity. The insertion of aromatic moieties between two carbon-carbon triple bonds offers an alternative design for dual Raman and fluorescence chromophores in biological imaging applications.

CHEMISTRY-A EUROPEAN JOURNAL (2021)

Article Chemistry, Multidisciplinary

Bithiophene-Cored, mono-, bis-, and tris-(Trimethylammonium)-Substituted, bis-Triarylborane Chromophores: Effect of the Number and Position of Charges on Cell Imaging and DNA/RNA Sensing

Sarina M. Berger et al.

Summary: This study presents the synthesis, photophysical, and electrochemical properties of selectively mono-, bis- and tris-dimethylamino- and trimethylammonium-substituted bis-triarylborane bithiophene chromophores, as well as the water solubility and singlet oxygen sensitizing efficiency of cationic compounds. The research highlights the significant influence of the bridging unit on the properties of bis-triarylboranes, especially the cationic compounds, and investigates their interactions with DNA, RNA, and DNApore in buffered solutions. Additionally, the study explores the compounds' ability to enter and localize within organelles of human lung carcinoma and normal lung cells, showing that both the number and distribution of charges on the chromophore affect interactions and staining properties.

CHEMISTRY-A EUROPEAN JOURNAL (2021)

Article Biochemistry & Molecular Biology

Triarylborane Dyes as a Novel Non-Covalent and Non-Inhibitive Fluorimetric Markers for DPP III Enzyme

Zeljka Ban et al.

Summary: Novel dyes were prepared by simple click CuAAC attachment, which interact specifically with proteins while their affinity to DNA/RNA is completely abolished. These dyes exhibit strong fluorescence enhancement upon binding to proteins, and the triarylborane-pyrene conjugate retains FRET effect when binding to the hDPP III enzyme.

MOLECULES (2021)

Review Chemistry, Organic

Polarization spectroscopy methods in the determination of interactions of small molecules with nucleic acids - tutorial

Tamara Smidlehner et al.

BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY (2018)

Review Food Science & Technology

Cyclodextrins in Food Technology and Human Nutrition: Benefits and Limitations

E. Fenyvesi et al.

CRITICAL REVIEWS IN FOOD SCIENCE AND NUTRITION (2016)

Article Chemistry, Multidisciplinary

Water-Soluble Triarylborane Chromophores for One- and Two-Photon Excited Fluorescence Imaging of Mitochondria in Cells

Stefanie Griesbeck et al.

CHEMISTRY-A EUROPEAN JOURNAL (2016)

Article Chemistry, Multidisciplinary

Strained Cyclooctyne as a Molecular Platform for Construction of Multimodal Imaging Probes

Yao Sun et al.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2015)

Review Chemistry, Multidisciplinary

Illuminating biological processes through site-specific protein labeling

Gong Zhang et al.

CHEMICAL SOCIETY REVIEWS (2015)

Article Chemistry, Physical

FRET-based probe for fluoride based on a phosphorescent iridium(III) complex containing triarylboron groups

Wenjuan Xu et al.

JOURNAL OF MATERIALS CHEMISTRY (2011)

Article Chemistry, Multidisciplinary

Rapid Cu-Free Click Chemistry with Readily Synthesized Biarylazacyclooctynones

John C. Jewett et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2010)

Review Chemistry, Multidisciplinary

Click Chemistry beyond Metal-Catalyzed Cycloaddition

C. Remzi Becer et al.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2009)

Article Pharmacology & Pharmacy

Sugammadex A Review of its Use in Anaesthetic Practice

Lily P. H. Yang et al.

DRUGS (2009)

Review Microscopy

A guided tour into subcellular colocalization analysis in light microscopy

S. Bolte et al.

JOURNAL OF MICROSCOPY (2006)

Article Chemistry, Multidisciplinary

A strain-promoted [3+2] azide-alkyne cycloaddition for covalent modification of blomolecules in living systems

NJ Agard et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2004)

Review Biochemistry & Molecular Biology

Analysis of thermal melting curves

JL Mergny et al.

OLIGONUCLEOTIDES (2003)

Article Chemistry, Analytical

Monofunctionalized β-cyclodextrins as sensor elements for the detection of small molecules

A Janshoff et al.

SENSORS AND ACTUATORS B-CHEMICAL (2000)