Cao Yanwei, Qin Yujiao, Bruist Michael, Gao Shang, Wang Bing, Wang Huixin, Guo Xinhua
College of Chemistry, Jilin University, Changchun, 130012, People's Republic of China.
J Am Soc Mass Spectrom. 2015 Jun;26(6):994-1003. doi: 10.1007/s13361-015-1093-2. Epub 2015 Apr 11.
Formation and dissociation of the interstrand i-motifs by DNA with the sequence d(X(n)C(4)Y(m)) (X and Y represent thymine, adenine, or guanine, and n, m range from 0 to 2) are studied with electrospray ionization mass spectrometry (ESI-MS), circular dichroism (CD), and UV spectrophotometry. The ion complexes detected in the gas phase and the melting temperatures (Tm) obtained in solution show that a non-C base residue located at 5' end favors formation of the four-stranded structures, with T > A > G for imparting stability. Comparatively, no rule is found when a non-C base is located at the 3' end. Detection of penta- and hexa-stranded ions indicates the formation of i-motifs with more than four strands. In addition, the i-motifs seen in our mass spectra are accompanied by single-, double-, and triple-stranded ions, and the trimeric ions were always less abundant during annealing and heat-induced dissociation process of the DNA strands in solution (pH = 4.5). This provides a direct evidence of a strand-by-strand formation and dissociation pathway of the interstrand i-motif and formation of the triple strands is the rate-limiting step. In contrast, the trimeric ions are abundant when the tetramolecular ions are subjected to collision-induced dissociation (CID) in the gas phase, suggesting different dissociation behaviors of the interstrand i-motif in the gas phase and in solution. Furthermore, hysteretic UV absorption melting and cooling curves reveal an irreversible dissociation and association kinetic process of the interstrand i-motif in solution.
采用电喷雾电离质谱(ESI-MS)、圆二色光谱(CD)和紫外分光光度法研究了序列为d(X(n)C(4)Y(m))(X和Y代表胸腺嘧啶、腺嘌呤或鸟嘌呤,n、m取值范围为0至2)的DNA链间i-基序的形成和解离。在气相中检测到的离子复合物以及在溶液中获得的解链温度(Tm)表明,位于5'端的非C碱基残基有利于四链结构的形成,其中T > A > G有助于提高稳定性。相比之下,当非C碱基位于3'端时未发现规律。五链和六链离子的检测表明形成了多于四条链的i-基序。此外,我们质谱图中出现的i-基序伴随着单链、双链和三链离子,并且在溶液(pH = 4.5)中DNA链的退火和热诱导解离过程中,三聚体离子的丰度始终较低。这为链间i-基序逐链形成和解离途径提供了直接证据,且三链的形成是限速步骤。相比之下,当四聚体离子在气相中进行碰撞诱导解离(CID)时,三聚体离子丰度较高,这表明链间i-基序在气相和溶液中的解离行为不同。此外,滞后的紫外吸收熔解和冷却曲线揭示了溶液中链间i-基序不可逆的解离和缔合动力学过程。