Identification and discrimination of binding sites of an organoruthenium anticancer complex to single-stranded oligonucleotides by mass spectrometry
Author:
Affiliation:
1. Beijing National Laboratory for Molecular Sciences
2. CAS Key Laboratory of Analytical Chemistry for Living Biosystems
3. Beijing Centre for Mass Spectrometry
4. Institute of Chemistry
5. Chinese Academy of Sciences
Abstract
Top-down MS analysis provided sequential and complementary fragments, which is more efficient than ladder-sequencing MS in discriminating binding sites of a ruthenium anticancer complex bearing a bulky ligand to oligonucleotides.
Publisher
Royal Society of Chemistry (RSC)
Subject
Electrochemistry,Spectroscopy,Environmental Chemistry,Biochemistry,Analytical Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2014/AN/C4AN00807C
Reference32 articles.
1. Inhibition of Cancer Cell Growth by Ruthenium(II) Arene Complexes
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3. Structure, Recognition, and Processing of Cisplatin−DNA Adducts
4. Organometallic Ruthenium(II) Diamine Anticancer Complexes: Arene-Nucleobase Stacking and Stereospecific Hydrogen-Bonding in Guanine Adducts
5. Highly Selective Binding of Organometallic Ruthenium Ethylenediamine Complexes to Nucleic Acids: Novel Recognition Mechanisms
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