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- Publisher Website: 10.1016/j.ultramic.2010.10.005
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- PMID: 21185457
- WOS: WOS:000286552200007
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Article: Quantification of the lateral detachment force for bacterial cells using atomic force microscope and centrifugation
Title | Quantification of the lateral detachment force for bacterial cells using atomic force microscope and centrifugation | ||||||
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Authors | |||||||
Keywords | Atomic force microscope Centrifugation Escherichia coli Lateral detachment force | ||||||
Issue Date | 2011 | ||||||
Publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/ultramic | ||||||
Citation | Ultramicroscopy, 2011, v. 111 n. 2, p. 131-139 How to Cite? | ||||||
Abstract | To determine the lateral detachment force for individual bacterial cells, a quantitative method using the contact mode of an atomic force microscope (AFM) was developed in this study. Three key factors for the proposed method, i.e. scan size, scan rate and cantilever choice, were evaluated and optimized. The scan size of 40×40γm2 was optimal for capturing sufficient number of adhered cells in a microscopic field and provide adequate information for cell identification and detachment force measurement. The scan rate affected the measurement results significantly, and was optimized at 40γm/s considering both force measurement accuracy and experimental efficiency. The hardness of applied cantilevers also influenced force determination. The proposed protocol for cantilever selection is to use those with the lowest spring constant first and then step up to a harder cantilever until all cells are detached. The lateral detachment force of Escherichia coli cells on polished stainless steel and a glass-slide coated with poly-l-lysine were measured as 0.763±0.167 and 0.639±0.136nN, respectively. The results showed that the established method had good repeatability and sensitivity to various bacteria/substrata combinations. The detachment force quantified by AFM (0.639±0.136nN) was comparable to that measured by the centrifugation method (1.12nN). © 2010 Elsevier B.V. | ||||||
Persistent Identifier | http://hdl.handle.net/10722/139034 | ||||||
ISSN | 2023 Impact Factor: 2.1 2023 SCImago Journal Rankings: 0.780 | ||||||
ISI Accession Number ID |
Funding Information: The authors wish to thank the Hong Kong UGC One-off Special Equipment Grant Scheme (SEG HKU10) for the financial support on this study, and Yuanqing Chao wishes to thank HKU for the postgraduate studentship. The technical assistance of Ms. Vicky Fung is greatly appreciated. The authors would also like to thank the reviewers for their comments. | ||||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Zhang, T | en_HK |
dc.contributor.author | Chao, Y | en_HK |
dc.contributor.author | Shih, K | en_HK |
dc.contributor.author | Li, XY | en_HK |
dc.contributor.author | Fang, HHP | en_HK |
dc.date.accessioned | 2011-09-23T05:44:27Z | - |
dc.date.available | 2011-09-23T05:44:27Z | - |
dc.date.issued | 2011 | en_HK |
dc.identifier.citation | Ultramicroscopy, 2011, v. 111 n. 2, p. 131-139 | en_HK |
dc.identifier.issn | 0304-3991 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/139034 | - |
dc.description.abstract | To determine the lateral detachment force for individual bacterial cells, a quantitative method using the contact mode of an atomic force microscope (AFM) was developed in this study. Three key factors for the proposed method, i.e. scan size, scan rate and cantilever choice, were evaluated and optimized. The scan size of 40×40γm2 was optimal for capturing sufficient number of adhered cells in a microscopic field and provide adequate information for cell identification and detachment force measurement. The scan rate affected the measurement results significantly, and was optimized at 40γm/s considering both force measurement accuracy and experimental efficiency. The hardness of applied cantilevers also influenced force determination. The proposed protocol for cantilever selection is to use those with the lowest spring constant first and then step up to a harder cantilever until all cells are detached. The lateral detachment force of Escherichia coli cells on polished stainless steel and a glass-slide coated with poly-l-lysine were measured as 0.763±0.167 and 0.639±0.136nN, respectively. The results showed that the established method had good repeatability and sensitivity to various bacteria/substrata combinations. The detachment force quantified by AFM (0.639±0.136nN) was comparable to that measured by the centrifugation method (1.12nN). © 2010 Elsevier B.V. | en_HK |
dc.language | eng | en_US |
dc.publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/ultramic | en_HK |
dc.relation.ispartof | Ultramicroscopy | en_HK |
dc.subject | Atomic force microscope | en_HK |
dc.subject | Centrifugation | en_HK |
dc.subject | Escherichia coli | en_HK |
dc.subject | Lateral detachment force | en_HK |
dc.subject.mesh | Bacterial Adhesion | - |
dc.subject.mesh | Centrifugation - methods | - |
dc.subject.mesh | Escherichia coli K12 - physiology | - |
dc.subject.mesh | Microscopy, Atomic Force - methods | - |
dc.subject.mesh | Reproducibility of Results | - |
dc.title | Quantification of the lateral detachment force for bacterial cells using atomic force microscope and centrifugation | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Zhang, T:zhangt@hkucc.hku.hk | en_HK |
dc.identifier.email | Shih, K:kshih@hkucc.hku.hk | en_HK |
dc.identifier.email | Li, XY:xlia@hkucc.hku.hk | en_HK |
dc.identifier.email | Fang, HHP:hrechef@hkucc.hku.hk | en_HK |
dc.identifier.authority | Zhang, T=rp00211 | en_HK |
dc.identifier.authority | Shih, K=rp00167 | en_HK |
dc.identifier.authority | Li, XY=rp00222 | en_HK |
dc.identifier.authority | Fang, HHP=rp00115 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.ultramic.2010.10.005 | en_HK |
dc.identifier.pmid | 21185457 | - |
dc.identifier.scopus | eid_2-s2.0-78449233654 | en_HK |
dc.identifier.hkuros | 192699 | en_US |
dc.identifier.hkuros | 208094 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-78449233654&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 111 | en_HK |
dc.identifier.issue | 2 | en_HK |
dc.identifier.spage | 131 | en_HK |
dc.identifier.epage | 139 | en_HK |
dc.identifier.isi | WOS:000286552200007 | - |
dc.publisher.place | Netherlands | en_HK |
dc.identifier.scopusauthorid | Zhang, T=24470677400 | en_HK |
dc.identifier.scopusauthorid | Chao, Y=36503486900 | en_HK |
dc.identifier.scopusauthorid | Shih, K=14072108900 | en_HK |
dc.identifier.scopusauthorid | Li, XY=26642887900 | en_HK |
dc.identifier.scopusauthorid | Fang, HHP=7402542625 | en_HK |
dc.identifier.citeulike | 8297634 | - |
dc.identifier.issnl | 0304-3991 | - |