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Article: Peak force tapping atomic force microscopy for advancing cell and molecular biology

TitlePeak force tapping atomic force microscopy for advancing cell and molecular biology
Authors
Issue Date2021
PublisherRSC Publications. The Journal's web site is located at http://pubs.rsc.org/en/journals/journalissues/nr#!recentarticles&all
Citation
Nanoscale, 2021, v. 13 n. 18, p. 8358-8375 How to Cite?
AbstractThe advent of atomic force microscopy (AFM) provides an exciting tool to detect molecular and cellular behaviors under aqueous conditions. AFM is able to not only visualize the surface topography of the specimens, but also can quantify the mechanical properties of the specimens by force spectroscopy assay. Nevertheless, integrating AFM topographic imaging with force spectroscopy assay has long been limited due to the low spatiotemporal resolution. In recent years, the appearance of a new AFM imaging mode called peak force tapping (PFT) has shattered this limit. PFT allows AFM to simultaneously acquire the topography and mechanical properties of biological samples with unprecedented spatiotemporal resolution. The practical applications of PFT in the field of life sciences in the past decade have demonstrated the excellent capabilities of PFT in characterizing the fine structures and mechanics of living biological systems in their native states, offering novel possibilities to reveal the underlying mechanisms guiding physiological/pathological activities. In this paper, the recent progress in cell and molecular biology that has been made with the utilization of PFT is summarized, and future perspectives for further progression and biomedical applications of PFT are provided.
Persistent Identifierhttp://hdl.handle.net/10722/309330
ISSN
2021 Impact Factor: 8.307
2020 SCImago Journal Rankings: 2.038
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLi, M-
dc.contributor.authorXi, N-
dc.contributor.authorLiu, L-
dc.date.accessioned2021-12-29T02:13:33Z-
dc.date.available2021-12-29T02:13:33Z-
dc.date.issued2021-
dc.identifier.citationNanoscale, 2021, v. 13 n. 18, p. 8358-8375-
dc.identifier.issn2040-3364-
dc.identifier.urihttp://hdl.handle.net/10722/309330-
dc.description.abstractThe advent of atomic force microscopy (AFM) provides an exciting tool to detect molecular and cellular behaviors under aqueous conditions. AFM is able to not only visualize the surface topography of the specimens, but also can quantify the mechanical properties of the specimens by force spectroscopy assay. Nevertheless, integrating AFM topographic imaging with force spectroscopy assay has long been limited due to the low spatiotemporal resolution. In recent years, the appearance of a new AFM imaging mode called peak force tapping (PFT) has shattered this limit. PFT allows AFM to simultaneously acquire the topography and mechanical properties of biological samples with unprecedented spatiotemporal resolution. The practical applications of PFT in the field of life sciences in the past decade have demonstrated the excellent capabilities of PFT in characterizing the fine structures and mechanics of living biological systems in their native states, offering novel possibilities to reveal the underlying mechanisms guiding physiological/pathological activities. In this paper, the recent progress in cell and molecular biology that has been made with the utilization of PFT is summarized, and future perspectives for further progression and biomedical applications of PFT are provided.-
dc.languageeng-
dc.publisherRSC Publications. The Journal's web site is located at http://pubs.rsc.org/en/journals/journalissues/nr#!recentarticles&all-
dc.relation.ispartofNanoscale-
dc.titlePeak force tapping atomic force microscopy for advancing cell and molecular biology-
dc.typeArticle-
dc.identifier.emailXi, N: xining@hku.hk-
dc.identifier.authorityXi, N=rp02044-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1039/D1NR01303C-
dc.identifier.pmid33913463-
dc.identifier.scopuseid_2-s2.0-85105989860-
dc.identifier.hkuros331227-
dc.identifier.volume13-
dc.identifier.issue18-
dc.identifier.spage8358-
dc.identifier.epage8375-
dc.identifier.isiWOS:000645254600001-
dc.publisher.placeUnited Kingdom-

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