Scalabrin Matteo, Palumbo Manlio, Richter Sara N
Department of Molecular Medicine, University of Padua , via Gabelli 63, 35121 Padua, Italy.
Department of Pharmaceutical and Pharmacological Sciences, University of Padua , via Marzolo 5, 35131 Padua, Italy.
Anal Chem. 2017 Sep 5;89(17):8632-8637. doi: 10.1021/acs.analchem.7b01282. Epub 2017 Aug 24.
G-quadruplexes are nucleic acids structures stabilized by physiological concentration of potassium ions. Because low stability G-quadruplexes are hardly detectable by mass spectrometry, we optimized solvent conditions: isopropanol in a triethylamine/hexafluoroisopropanol mixture highly increased G-quadruplex sensitivity with no modification of the physiological G-quadruplex conformation. G-quadruplexes/G-quadruplex-ligand complexes were also correctly detected at concentration as low as 40 nM. Detection of the physiological conformation of G4s and their complexes opens up the possibility to perform high-throughput screening of G-quadruplex ligands for the development of drug molecules effective against critical human diseases.
G-四链体是由生理浓度的钾离子稳定的核酸结构。由于低稳定性的G-四链体很难通过质谱检测到,我们优化了溶剂条件:在三乙胺/六氟异丙醇混合物中加入异丙醇,可显著提高G-四链体的灵敏度,且不会改变其生理构象。G-四链体/G-四链体配体复合物在低至40 nM的浓度下也能被正确检测到。对G4及其复合物的生理构象进行检测,为高通量筛选G-四链体配体以开发治疗重大人类疾病的有效药物分子开辟了可能性。