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Effect of Terminal Phosphate Groups on Collisional Dissociation of RNA Oligonucleotide Anions.
Zuo, Mei-Qing; Song, Ge; Zhang, Ji-Shuai; Dong, Meng-Qiu; Sun, Rui-Xiang.
Afiliación
  • Zuo MQ; National Institute of Biological Sciences, Beijing 102206, China.
  • Song G; Tsinghua Institute of Multidisciplinary Biomedical Research, Tsinghua University, Beijing 100084, China.
  • Zhang JS; National Institute of Biological Sciences, Beijing 102206, China.
  • Dong MQ; Tsinghua Institute of Multidisciplinary Biomedical Research, Tsinghua University, Beijing 100084, China.
  • Sun RX; Synthetic and Functional Biomolecules Center, Beijing National Laboratory for Molecular Sciences, Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China.
J Am Soc Mass Spectrom ; 35(9): 2090-2101, 2024 Sep 04.
Article en En | MEDLINE | ID: mdl-39136314
ABSTRACT
The increasing need for mass spectrometric analysis of RNA molecules calls for a better understanding of their gas-phase fragmentation behaviors. In this study, we investigate the effect of terminal phosphate groups on the fragmentation spectra of RNA oligonucleotides (oligos) using high-resolution mass spectrometry (MS). Negative-ion mode collision-induced dissociation (CID) and higher-energy collisional dissociation (HCD) were carried out on RNA oligos containing a terminal phosphate group on either end, both ends, or neither end. We find that terminal phosphate groups affect the fragmentation behavior of RNA oligos in a way that is dependent on the precursor charge state and the oligo length. Specifically, for precursor ions of RNA oligos of the same sequence, those with 5'- or 3'-phosphate, or both, have a higher charge state distribution and lose the phosphate group(s) in the form of a neutral (H3PO4 or HPO3) or an anion ([H2PO4]- or [PO3]-) upon CID or HCD. Such a neutral or charged loss is most conspicuous for precursor ions of an intermediate charge state, e.g., 3- for 4-nt oligos or 4- and 5- for 8-nt oligos. This decreases the intensity of sequencing ions (a-, a-B, b-, c-, d-, w-, x-, y-, z-ions) and hence is unfavorable for sequencing by CID or HCD. Removal of terminal phosphate groups by calf intestinal alkaline phosphatase improved MS analysis of RNA oligos. Additionally, the intensity of a fragment ion at m/z 158.925, which we identified as a dehydrated pyrophosphate anion ([HP2O6]-), is markedly increased by the presence of a terminal phosphate group. These findings expand the knowledge base necessary for software development for MS analysis of RNA.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Fosfatos / ARN / Aniones Idioma: En Revista: J Am Soc Mass Spectrom Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Fosfatos / ARN / Aniones Idioma: En Revista: J Am Soc Mass Spectrom Año: 2024 Tipo del documento: Article