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- Publisher Website: 10.1021/ja2013278
- Scopus: eid_2-s2.0-79955881998
- PMID: 21517022
- WOS: WOS:000290782200031
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Article: Tracking bismuth antiulcer drug uptake in single helicobacter pylori cells
Title | Tracking bismuth antiulcer drug uptake in single helicobacter pylori cells | ||||||||
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Authors | |||||||||
Issue Date | 2011 | ||||||||
Publisher | American Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/jacsat/index.html | ||||||||
Citation | Journal Of The American Chemical Society, 2011, v. 133 n. 19, p. 7355-7357 How to Cite? | ||||||||
Abstract | Bismuth-based drugs have long been used for the treatment of Helicobacter pylori infection. In this work, the metal content in H. pylori was monitored at the single-cell level by time-resolved inductively coupled plasma mass spectrometry, and ∼2.9 × 107 Mg atoms/cell was determined for the wild-type. Bacteria treated with a Bi antiulcer drug deposited nearly 1.0 × 106 Bi atoms/cell, whereas the uptake process took ∼3 h to reach the half-maximum. Interference of ferric ions on bismuth uptake was demonstrated, suggesting that the metallodrug can utilize certain iron-transport pathways in the pathogen. The approach provides a general strategy for monitoring metals in single cells, facilitating exploration of metal-relevant bioprocesses. © 2011 American Chemical Society. | ||||||||
Persistent Identifier | http://hdl.handle.net/10722/137219 | ||||||||
ISSN | 2023 Impact Factor: 14.4 2023 SCImago Journal Rankings: 5.489 | ||||||||
ISI Accession Number ID |
Funding Information: This work was supported by the Research Grants Council of Hong Kong SAR, P. R. China (Projects HKU7043/06P, HKU1/07C, HKU7042/07P, HKU7006/09P, HKU7049/09P, and N_HKU752/09), the Croucher Foundation, and the Seed Funding Scheme for Basic Research of the University of Hong Kong. C.N.T. is grateful to F. Ng and Prof. B. J. Zheng from the LKS Faculty of Medicine, HKU, for assistance with H. pylori culture at the initial stage of the project. | ||||||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Tsang, CN | en_HK |
dc.contributor.author | Ho, KS | en_HK |
dc.contributor.author | Sun, H | en_HK |
dc.contributor.author | Chan, WT | en_HK |
dc.date.accessioned | 2011-08-26T14:19:14Z | - |
dc.date.available | 2011-08-26T14:19:14Z | - |
dc.date.issued | 2011 | en_HK |
dc.identifier.citation | Journal Of The American Chemical Society, 2011, v. 133 n. 19, p. 7355-7357 | en_HK |
dc.identifier.issn | 0002-7863 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/137219 | - |
dc.description.abstract | Bismuth-based drugs have long been used for the treatment of Helicobacter pylori infection. In this work, the metal content in H. pylori was monitored at the single-cell level by time-resolved inductively coupled plasma mass spectrometry, and ∼2.9 × 107 Mg atoms/cell was determined for the wild-type. Bacteria treated with a Bi antiulcer drug deposited nearly 1.0 × 106 Bi atoms/cell, whereas the uptake process took ∼3 h to reach the half-maximum. Interference of ferric ions on bismuth uptake was demonstrated, suggesting that the metallodrug can utilize certain iron-transport pathways in the pathogen. The approach provides a general strategy for monitoring metals in single cells, facilitating exploration of metal-relevant bioprocesses. © 2011 American Chemical Society. | en_HK |
dc.language | eng | en_US |
dc.publisher | American Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/jacsat/index.html | en_HK |
dc.relation.ispartof | Journal of the American Chemical Society | en_HK |
dc.subject.mesh | Anti-Ulcer Agents - pharmacokinetics | - |
dc.subject.mesh | Biological Transport | - |
dc.subject.mesh | Bismuth - pharmacokinetics | - |
dc.subject.mesh | Helicobacter pylori - metabolism | - |
dc.title | Tracking bismuth antiulcer drug uptake in single helicobacter pylori cells | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Sun, H:hsun@hkucc.hku.hk | en_HK |
dc.identifier.email | Chan, WT:wtchan@hku.hk | en_HK |
dc.identifier.authority | Sun, H=rp00777 | en_HK |
dc.identifier.authority | Chan, WT=rp00668 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1021/ja2013278 | en_HK |
dc.identifier.pmid | 21517022 | - |
dc.identifier.scopus | eid_2-s2.0-79955881998 | en_HK |
dc.identifier.hkuros | 189542 | en_US |
dc.identifier.hkuros | 232301 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-79955881998&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 133 | en_HK |
dc.identifier.issue | 19 | en_HK |
dc.identifier.spage | 7355 | en_HK |
dc.identifier.epage | 7357 | en_HK |
dc.identifier.eissn | 1520-5126 | - |
dc.identifier.isi | WOS:000290782200031 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Tsang, CN=36624389600 | en_HK |
dc.identifier.scopusauthorid | Ho, KS=36162334100 | en_HK |
dc.identifier.scopusauthorid | Sun, H=7404827446 | en_HK |
dc.identifier.scopusauthorid | Chan, WT=7403918827 | en_HK |
dc.identifier.issnl | 0002-7863 | - |