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Study of interactions between actinomycin D and oligonucleotides by microchip electrophoresis and ESI-MS
In the present study, the interactions between actinomycin D (ActD) and single stranded DNA (ssDNA) 5′-CGTAACCAACTGCAACGT-3′ and a duplex stranded DNA (dsDNA) with this sequence were investigated by microchip-based non-gel sieving electrophoresis and electrospray ionization mass spectrometry (ESI-MS...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier B.V.
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111764/ https://www.ncbi.nlm.nih.gov/pubmed/19071655 http://dx.doi.org/10.1016/j.talanta.2006.11.019 |
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author | Zhou, Xiaomian Shen, Zheng Li, Dazhi He, Xinya Lin, Bingcheng |
author_facet | Zhou, Xiaomian Shen, Zheng Li, Dazhi He, Xinya Lin, Bingcheng |
author_sort | Zhou, Xiaomian |
collection | PubMed |
description | In the present study, the interactions between actinomycin D (ActD) and single stranded DNA (ssDNA) 5′-CGTAACCAACTGCAACGT-3′ and a duplex stranded DNA (dsDNA) with this sequence were investigated by microchip-based non-gel sieving electrophoresis and electrospray ionization mass spectrometry (ESI-MS). The ssDNA was designed according to the conserved regions of open reading frame 1b (replicase 1B) following the Tor 2 SARS genome sequence of 15611-15593. The binding constants of the interactions between ActD and ssDNA/dsDNA were (8.3 ± 0.32) × 10(6) M(−1) (ssDNA) and (2.8 ± 0.02) × 10(5) M(−1) (dsDNA), respectively, calculated from microchip electrophoresis via Scatchard plot. The binding stoichiometries were 1:1 (single/1ActD molecule) and 1:2 (duplex/2ActD molecules) calculated from microchip electrophoresis, and the results were further verified by ESI-MS. The results obtained by these two methods indicated that ActD bound much more tightly to ssDNA used in this work than dsDNA. Furthermore, this is shown that the microchip-based non-gel sieving electrophoresis method is a rapid, highly sensitive and convenient method for the studies of interactions between DNA and small molecule drugs. |
format | Online Article Text |
id | pubmed-7111764 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Published by Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71117642020-04-02 Study of interactions between actinomycin D and oligonucleotides by microchip electrophoresis and ESI-MS Zhou, Xiaomian Shen, Zheng Li, Dazhi He, Xinya Lin, Bingcheng Talanta Article In the present study, the interactions between actinomycin D (ActD) and single stranded DNA (ssDNA) 5′-CGTAACCAACTGCAACGT-3′ and a duplex stranded DNA (dsDNA) with this sequence were investigated by microchip-based non-gel sieving electrophoresis and electrospray ionization mass spectrometry (ESI-MS). The ssDNA was designed according to the conserved regions of open reading frame 1b (replicase 1B) following the Tor 2 SARS genome sequence of 15611-15593. The binding constants of the interactions between ActD and ssDNA/dsDNA were (8.3 ± 0.32) × 10(6) M(−1) (ssDNA) and (2.8 ± 0.02) × 10(5) M(−1) (dsDNA), respectively, calculated from microchip electrophoresis via Scatchard plot. The binding stoichiometries were 1:1 (single/1ActD molecule) and 1:2 (duplex/2ActD molecules) calculated from microchip electrophoresis, and the results were further verified by ESI-MS. The results obtained by these two methods indicated that ActD bound much more tightly to ssDNA used in this work than dsDNA. Furthermore, this is shown that the microchip-based non-gel sieving electrophoresis method is a rapid, highly sensitive and convenient method for the studies of interactions between DNA and small molecule drugs. Published by Elsevier B.V. 2007-04-30 2006-12-21 /pmc/articles/PMC7111764/ /pubmed/19071655 http://dx.doi.org/10.1016/j.talanta.2006.11.019 Text en Copyright © 2006 Published by Elsevier B.V. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Zhou, Xiaomian Shen, Zheng Li, Dazhi He, Xinya Lin, Bingcheng Study of interactions between actinomycin D and oligonucleotides by microchip electrophoresis and ESI-MS |
title | Study of interactions between actinomycin D and oligonucleotides by microchip electrophoresis and ESI-MS |
title_full | Study of interactions between actinomycin D and oligonucleotides by microchip electrophoresis and ESI-MS |
title_fullStr | Study of interactions between actinomycin D and oligonucleotides by microchip electrophoresis and ESI-MS |
title_full_unstemmed | Study of interactions between actinomycin D and oligonucleotides by microchip electrophoresis and ESI-MS |
title_short | Study of interactions between actinomycin D and oligonucleotides by microchip electrophoresis and ESI-MS |
title_sort | study of interactions between actinomycin d and oligonucleotides by microchip electrophoresis and esi-ms |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111764/ https://www.ncbi.nlm.nih.gov/pubmed/19071655 http://dx.doi.org/10.1016/j.talanta.2006.11.019 |
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