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Interactions of Protonated Guanidine and Guanidine Derivatives with Multiply Deprotonated RNA Probed by Electrospray Ionization and Collisionally Activated Dissociation

机译:电喷雾电离和碰撞活化解离探测质子化的胍和胍衍生物与多重去质子化的RNA的相互作用。

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Abstract Interactions of ribonucleic acid (RNA) with guanidine and guanidine derivatives are important features in RNA?¢????protein and RNA?¢????drug binding. Here we have investigated noncovalently bound complexes of an 8-nucleotide RNA and six different ligands, all of which have a guanidinium moiety, by using electrospray ionization (ESI) and collisionally activated dissociation (CAD) mass spectrometry (MS). The order of complex stability correlated almost linearly with the number of ligand atoms that can potentially be involved in hydrogen-bond or salt-bridge interactions with the RNA, but not with the proton affinity of the ligands. However, ligand dissociation of the complex ions in CAD was generally accompanied by proton transfer from ligand to RNA, which indicated conversion of salt-bridge into hydrogen-bond interactions. The relative stabilities and dissociation pathways of [RNA+ m L?¢???? n H] n ?¢???? complexes with different stoichiometries ( m =1?¢????5) and net charge ( n = 2?¢????5) revealed both specific and unspecific ligand binding to the RNA.
机译:摘要核糖核酸(RNA)与胍和胍衍生物的相互作用是RNA与蛋白质和RNA与药物结合的重要特征。在这里,我们通过电喷雾电离(ESI)和碰撞活化解离(CAD)质谱法研究了8个核苷酸RNA和六个不同配体(均具有胍基部分)的非共价结合复合物。复杂稳定性的顺序几乎与可能与RNA进行氢键或盐桥相互作用的配体原子数线性相关,但与配体的质子亲和力无关。然而,CAD中复合离子的配体解离通常伴随着质子从配体向RNA的转移,这表明盐桥转换为氢键相互作用。 [RNA + m L + +的相对稳定性和解离途径n H] n?¢ ????具有不同化学计量比(m =1≤5≤5)和净电荷(n =2≤2≤5)的复合物揭示了特异性和非特异性配体与RNA的结合。

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