Related Experiment Video
Updated: May 26, 2025

Preparation of a Corannulene-functionalized Hexahelicene by CopperI-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
Published on: September 18, 2016
Calixarenes meet (TG4T)4 G-quadruplex: Exploring reciprocal interactions to develop innovative biotechnological
Andrea Patrizia Falanga1, Maria Cremonini2, Alessio Bartocci3
1Department of Pharmacy, University of Naples Federico II, Via Domenico Montesano 49, 80131 Naples, Italy.
Calixarene ligands interact with G-quadruplex (GQ) DNA, crucial for gene regulation and telomere maintenance. Ligand structure dictates binding sites, offering potential for therapeutic applications targeting DNA structures.
Area of Science:
- Biochemistry
- Molecular Biology
- Medicinal Chemistry
Background:
- G-quadruplex (GQ) DNA structures are vital in regulating gene expression, telomere maintenance, genome stability, and DNA repair.
- Understanding interactions with GQ DNA is crucial for developing novel therapeutic and biotechnological tools.
Purpose of the Study:
- To investigate the interaction between calixarene ligands and G-quadruplex (GQ) DNA assemblies for the first time.
- To analyze how different functional groups on calixarene ligands affect their binding affinity and specificity towards GQ DNA.
Main Methods:
- Circular dichroism (CD) spectroscopy
- Nuclear Magnetic Resonance (NMR) spectroscopy
- Molecular dynamics (MD) simulations
Main Results:
- Both cationic and zwitterionic calixarene derivatives showed favorable interactions with a model GQ DNA.
- Calixarene ligands induced GQ DNA aggregation at higher concentrations.
- Ligand-GQ interaction specificity varied based on functional groups: proline-rich calixarene favored GQ termini, while guanidinium-functionalized calixarene preferred phosphate groups.
Conclusions:
- Calixarene ligands can recognize and bind to specific structural features of G-quadruplex DNA.
- The functional groups on calixarene upper rims determine their binding selectivity.
- These findings support the development of calixarenes as targeted GQ ligands for therapeutic and biotechnological applications.
Related Concept Videos
Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group...
Electrophilic Addition to Alkynes: Halogenation
Halogenation is another class of electrophilic addition reactions where a halogen molecule gets added across a π bond. In alkynes, the presence of two π bonds allows for the addition of two equivalents of halogens (bromine or chlorine). The addition of the first halogen molecule forms a trans-dihaloalkene as the major product and the cis isomer as the minor product. Subsequent addition of the second equivalent yields the tetrahalide.
Radicals: Electronic Structure and Geometry
Accordingly, the structure of a trivalent radical lies between the geometries of carbocations and carbanions. An sp2-hybridized carbocation is trigonal planar, while an sp3-hybridized carbanion is trigonal pyramidal. Here, the difference in geometry is...
Thermal and Photochemical Electrocyclic Reactions: Overview
Chair Conformation of Cyclohexane
The hydrogen atoms linked to carbons are arranged in two different axial and equatorial orientations to achieve this...
Cycloalkanes
The IUPAC nomenclature of cycloalkanes follows similar rules that apply to...

