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Article: Cell lysis inside the capillary facilitated by transverse diffusion of laminar flow profiles (TDLFP)

TitleCell lysis inside the capillary facilitated by transverse diffusion of laminar flow profiles (TDLFP)
Authors
KeywordsCell lysis
Transverse diffusion of laminar flow profiles
Single-cell analysis
Chemical cytometry
Issue Date2007
Citation
Analytical and Bioanalytical Chemistry, 2007, v. 387, n. 1, p. 91-96 How to Cite?
AbstractChemical cytometry studies the molecular composition of individual cells by means of capillary electrophoresis or capillary chromatography. In one of its realizations an intact cell is injected inside the capillary, the plasma membrane is disrupted to release the cellular contents into the separation buffer, and, finally, the molecules of interest are separated and detected. The solubilization of the plasma membrane with a surfactant is a simple and efficient way of achieving cell lysis inside the capillary. To facilitate cell lysis by a surfactant the cell has to be contacted with the surfactant inside the capillary. We recently introduced a generic method for mixing solutions inside the capillary termed transverse diffusion of laminar flow profiles (TDLFP). In this work, we propose that TDLFP can facilitate efficient cell lysis inside the capillary. Conceptually, a short plug of the surfactant is injected by pressure prior to cell injection. The cell is then injected by pressure wizthin a plug of the physiological buffer. Due to the parabolic profiles of pressure-driven laminar flows the interface between the plug of the surfactant and that of the physiological buffer is predominantly longitudinal. Transverse diffusion mixes the surfactant with the physiological buffer, which leads to surfactant's contact with the cell and subsequent cell lysis. Here, we demonstrate that the proposed concept is valid. TDLFP-facilitated cell lysis by a short plug of the surfactant allows us to exclude the surfactant from the run buffer, and, hence, facilitates modes of separation, which are incompatible with the surfactant's presence in the run buffer. In addition to cell lysis, TDLFP will be used to mix the cellular components with labeling reactants, affinity probes, inhibitors, etc. We foresee that the generic nature and enabling capabilities of TDLFP will speed up the maturation of chemical cytometry into a practical bioanalytical tool.
Persistent Identifierhttp://hdl.handle.net/10722/291771
ISSN
2023 Impact Factor: 3.8
2023 SCImago Journal Rankings: 0.686
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorBerezovski, Maxim V.-
dc.contributor.authorMak, Tak W.-
dc.contributor.authorKrylov, Sergey N.-
dc.date.accessioned2020-11-17T14:55:05Z-
dc.date.available2020-11-17T14:55:05Z-
dc.date.issued2007-
dc.identifier.citationAnalytical and Bioanalytical Chemistry, 2007, v. 387, n. 1, p. 91-96-
dc.identifier.issn1618-2642-
dc.identifier.urihttp://hdl.handle.net/10722/291771-
dc.description.abstractChemical cytometry studies the molecular composition of individual cells by means of capillary electrophoresis or capillary chromatography. In one of its realizations an intact cell is injected inside the capillary, the plasma membrane is disrupted to release the cellular contents into the separation buffer, and, finally, the molecules of interest are separated and detected. The solubilization of the plasma membrane with a surfactant is a simple and efficient way of achieving cell lysis inside the capillary. To facilitate cell lysis by a surfactant the cell has to be contacted with the surfactant inside the capillary. We recently introduced a generic method for mixing solutions inside the capillary termed transverse diffusion of laminar flow profiles (TDLFP). In this work, we propose that TDLFP can facilitate efficient cell lysis inside the capillary. Conceptually, a short plug of the surfactant is injected by pressure prior to cell injection. The cell is then injected by pressure wizthin a plug of the physiological buffer. Due to the parabolic profiles of pressure-driven laminar flows the interface between the plug of the surfactant and that of the physiological buffer is predominantly longitudinal. Transverse diffusion mixes the surfactant with the physiological buffer, which leads to surfactant's contact with the cell and subsequent cell lysis. Here, we demonstrate that the proposed concept is valid. TDLFP-facilitated cell lysis by a short plug of the surfactant allows us to exclude the surfactant from the run buffer, and, hence, facilitates modes of separation, which are incompatible with the surfactant's presence in the run buffer. In addition to cell lysis, TDLFP will be used to mix the cellular components with labeling reactants, affinity probes, inhibitors, etc. We foresee that the generic nature and enabling capabilities of TDLFP will speed up the maturation of chemical cytometry into a practical bioanalytical tool.-
dc.languageeng-
dc.relation.ispartofAnalytical and Bioanalytical Chemistry-
dc.subjectCell lysis-
dc.subjectTransverse diffusion of laminar flow profiles-
dc.subjectSingle-cell analysis-
dc.subjectChemical cytometry-
dc.titleCell lysis inside the capillary facilitated by transverse diffusion of laminar flow profiles (TDLFP)-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1007/s00216-006-0866-7-
dc.identifier.pmid17066286-
dc.identifier.scopuseid_2-s2.0-33845656089-
dc.identifier.volume387-
dc.identifier.issue1-
dc.identifier.spage91-
dc.identifier.epage96-
dc.identifier.eissn1618-2650-
dc.identifier.isiWOS:000242968000018-
dc.identifier.issnl1618-2642-

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