Madhusudanan K P, Katti S B, Vijayalakshmi R, Nair B U
Central Drug Research Institute, Lucknow-226001, India.
J Mass Spectrom. 1999 Aug;34(8):880-4. doi: 10.1002/(SICI)1096-9888(199908)34:8<880::AID-JMS844>3.0.CO;2-E.
Interactions of [Cr(salprn)(H(2)O)(2)]ClO(4) with nucleosides and dinucleotides were studied using electrospray ionization mass spectrometry. The nucleosides 2'-deoxycytidine, thymidine, 2'-deoxyadenosine, 2'-deoxyguanosine, cytidine, adenosine and guanosine form 1 : 1 and 2 : 1 adducts with Cr(salprn), whereas the dinucleotides CpG, GpC, ApT, TpA and TpC form only the 1 : 1 adducts. Collisional activation (CA) spectra of these adducts reveal that Cr(+) attaches to the bases in nucleosides and to both the phosphate and base, especially cytosine and guanine moieties, in the nucleotides. The sugar residues appear to offer no binding sites as elimination of sugar residues is fairly abundant in the CA spectra of the adducts of many of the nucleosides.
使用电喷雾电离质谱法研究了[Cr(salprn)(H₂O)₂]ClO₄与核苷和二核苷酸的相互作用。核苷2'-脱氧胞苷、胸苷、2'-脱氧腺苷、2'-脱氧鸟苷、胞苷、腺苷和鸟苷与[Cr(salprn)]⁺形成1:1和2:1加合物,而二核苷酸CpG、GpC、ApT、TpA和TpC仅形成1:1加合物。这些加合物的碰撞活化(CA)光谱表明,Cr⁺与核苷中的碱基以及核苷酸中的磷酸和碱基,特别是胞嘧啶和鸟嘌呤部分结合。糖残基似乎不提供结合位点,因为在许多核苷加合物的CA光谱中,糖残基的消除相当丰富。