DNA G-quadruplexes (G4s) are key structures for the development of targeted anticancer therapies. In this context, ligands selectively interacting with G4s can represent valuable anticancer drugs. Aiming at speeding up the identification of G4-targeting synthetic or natural compounds, we developed an affinity chromatography-based assay, named G-quadruplex on Oligo Affinity Support (G4-OAS), by synthesizing G4-forming sequences on commercially available polystyrene OAS. Then, due to unspecific binding of several hydrophobic ligands on nude OAS, we moved to Controlled Pore Glass (CPG). We thus conceived an ad hoc functionalized, universal support on which both the on-support elongation and deprotection of the G4-forming oligonucleotides can be performed, along with the successive affinity chromatography-based assay, renamed as G-quadruplex on Controlled Pore Glass (G4-CPG) assay. Here we describe these assays and their applications to the screening of several libraries of chemically different putative G4 ligands. Finally, ongoing studies and outlook of our G4-CPG assay are reported.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9127747PMC
http://dx.doi.org/10.1002/open.202200090DOI Listing

Publication Analysis

Top Keywords

affinity chromatography-based
12
chromatography-based assay
8
controlled pore
8
pore glass
8
g4-cpg assay
8
affinity
4
chromatography-based assays
4
assays screening
4
screening potential
4
ligands
4

Similar Publications

Non-immunoglobin scaffold binders as efficient affinity ligands for purification of broad-spectrum serum albumins.

Talanta

November 2024

Division of Abdominal Tumor Multimodality Treatment, Cancer Center, NHC Key Lab of Transplant Engineering and Immunology, Regenerative Medicine Research Center, West China Hospital, Sichuan University, Chengdu, 610041, China; Sichuan Provincial Engineering Laboratory of Pathology in Clinical Application, West China Hospital, Sichuan University, Chengdu, 610041, China; Institutes for Systems Genetics, Frontiers Science Center for Disease-Related Molecular Network, West China Hospital, Sichuan University, Chengdu, 610041, China. Electronic address:

Although non-immunoglobin scaffold binders with high affinity and broad spectrum for albumin are attractive for lab-scale albumin purification, affinity chromatography based on these binders has not been developed. Here, the albumin-binding capabilities of representative binders, including protein G-derived albumin binding domain (ABD), albumin binding nanofitins (ABNF), and human serum albumin affimer 31 (HSA31) were predicted by interaction structure analysis and verified by experimental assays. Interaction structure prediction suggested that ABD possessed great potential to bind human (HSA), rhesus monkey (RhSA), mouse (MSA), and rat serum albumin (RSA), whereas ABNF might only bind HSA and bovine serum albumin (BSA), and HSA31 might not bind any of the tested albumins.

View Article and Find Full Text PDF

Rapid analysis of amatoxins in human urine by means of affinity column chromatography and liquid chromatography-high-resolution tandem mass spectrometry.

Sci Rep

September 2024

Department of Experimental and Clinical Toxicology, Institute of Experimental and Clinical Pharmacology and Toxicology, Center for Molecular Signaling (PZMS), Saarland University, Kirrberger Str., Building 46, 66421, Homburg, Germany.

Article Synopsis
  • Amatoxins, which are cyclic peptides, are responsible for a significant number of fatalities each year, making their analysis crucial for public health.
  • The study introduces a novel analytical method using affinity column chromatography with a specific monoclonal antibody and high-resolution mass spectrometry to detect low levels of amatoxins in human urine samples, achieving a sensitivity of 1 ng/mL.
  • The new procedure has been validated for specific amatoxins and can determine acute intoxications within 90 minutes, suggesting that similar techniques could be applied to analyze other toxic peptides effectively.
View Article and Find Full Text PDF

CeO nanocages with tetra-enzyme mimetic activities for dual-channel ratiometric colorimetric detection of microcystins-LR.

Anal Chim Acta

June 2024

School of Chemistry and Environmental Engineering, Wuhan Institute of Technology, Wuhan, 430205, PR China. Electronic address:

Background: Microcystin-leucine-arginine (MC-LR) produced by various cyanobacteria during harmful algal bloom poses serious threats to drinking water safety and human health. Conventional chromatography-based detection methods require expensive instruments and complicated sample pretreatment, limiting their application for on-site detection. Colorimetric aptasensors are simple and rapid, and are amenable to fast detection.

View Article and Find Full Text PDF

Insights into nucleoside hydrolase from Leishmania donovani inhibition: A new bioaffinity chromatography-based screening assay and docking studies.

Bioorg Chem

May 2024

BioCrom, Laboratório de Cromatografia de Bioafinidade e Química Ambiental, Departamento de Química Orgânica, Instituto de Química, Universidade Federal Fluminense (UFF), Niterói, Brazil. Electronic address:

Article Synopsis
  • Leishmaniasis is a serious health issue, particularly visceral leishmaniasis, and targeting nucleoside hydrolase (NH) could lead to new treatments.
  • Researchers developed immobilized enzyme reactors (IMERs) using LdNH to monitor enzyme activity in real-time during liquid chromatography, successfully separating the substrate and product.
  • The study identified new inhibitors, with one compound showing promising effectiveness and provided insights for designing better inhibitors through molecular modeling techniques.
View Article and Find Full Text PDF

Background: Today, numerous antimicrobial and anticancer properties have been reported for plant lectins due to their ability to bind to carbohydrates. The agglutinin (UDA lectin) is a monomeric, small, and low molecular weight glycoprotein. It has attracted the attention of many researchers for identification, treatment, and other clinical purposes.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!