Solution NMR Structure of a Ligand/Hybrid-2-G-Quadruplex Complex Reveals Rearrangements that Affect Ligand Binding.

Angew Chem Int Ed Engl

Institute for Organic Chemistry and Chemical Biology, Center of Biomolecular Magnetic Resonance (BMRZ), Goethe University Frankfurt/Main, Max-von-Laue-Strasse 7, 60439, Frankfurt, Germany.

Published: June 2017


Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Telomeric G-quadruplexes have recently emerged as drug targets in cancer research. Herein, we present the first NMR structure of a telomeric DNA G-quadruplex that adopts the biologically relevant hybrid-2 conformation in a ligand-bound state. We solved the complex with a metalorganic gold(III) ligand that stabilizes G-quadruplexes. Analysis of the free and bound structures reveals structural changes in the capping region of the G-quadruplex. The ligand is sandwiched between one terminal G-tetrad and a flanking nucleotide. This complex structure involves a major structural rearrangement compared to the free G-quadruplex structure as observed for other G-quadruplexes in different conformations, invalidating simple docking approaches to ligand-G-quadruplex structure determination.

Download full-text PDF

Source
http://dx.doi.org/10.1002/anie.201702135DOI Listing

Publication Analysis

Top Keywords

nmr structure
8
structure
5
solution nmr
4
structure ligand/hybrid-2-g-quadruplex
4
ligand/hybrid-2-g-quadruplex complex
4
complex reveals
4
reveals rearrangements
4
rearrangements affect
4
affect ligand
4
ligand binding
4

Similar Publications

Importance: Cannabis is the most commonly used illicit drug, with 10% to 30% of regular users developing cannabis use disorder (CUD), a condition linked to altered hippocampal integrity. Evidence suggests high-intensity interval training (HIIT) enhances hippocampal structure and function, with this form of physical exercise potentially mitigating CUD-related cognitive and mental health impairments.

Objective: To determine the impact of a 12-week HIIT intervention on hippocampal integrity (ie, structure, connectivity, biochemistry) compared with 12 weeks of strength and resistance (SR) training in CUD.

View Article and Find Full Text PDF

What are we missing? What are we assuming? The need to foster feature discovery tools to improve statistical models.

Cereb Cortex

August 2025

Section on Functional Imaging Methods & Functional MRI Core Facility, National Institute of Mental Health, 10 Center Drive, Rm 1D80, Bethesda, MD 20892, United States.

Statistical Parametric Mapping (SPM) has been profoundly influential to neuroimaging as it has fostered rigorous, statistically grounded structure for model-based inferences that have led to mechanistic insights about the human brain over the past 30 years. The statistical constructs shared with the world through SPM have been instrumental for deriving meaning from neuroimaging data; however, they require simplifying assumptions which can provide results that, while statistically sound, may not accurately reflect the mechanisms of brain function. A platform that fosters the exploration of the rich and varying neuronal and physiologic underpinnings of the measured signals and their associations to behavior and physiologic measures needs a different set of tools.

View Article and Find Full Text PDF

The anterior commissure (AC) has an anterior and posterior limb. Despite comprehensive information about the posterior limb, there is limited and conflicting information about the anterior limb in the literature. We aimed to show the anatomical relationships of the AC with neighboring structures by using white matter microdissection and magnetic resonance (MR) tractography, primarily on the anterior limb of the AC.

View Article and Find Full Text PDF

We have established a new route for boron-rich ruthenaborane clusters utilizing [BH·THF] and a ruthenium precursor featuring chelating ligands. Salt elimination reactions between [K(CHNE)], (E = S; Se) and [RuCl(PPh)], afforded -[Ru(κ--CHNE)(PPh)], -- (-: E = S and -: E = Se). Following the ligand exchange reaction with the 1,2-bis (diphenylphosphino)ethane (dppe) ligand yielded -[Ru(κ--CHNE)(dppe)] (-: E = S; -: E = Se).

View Article and Find Full Text PDF