Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/117016
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dc.contributorDepartment of Electrical and Electronic Engineeringen_US
dc.creatorWang, Yen_US
dc.creatorXue, Yen_US
dc.creatorWang, Hen_US
dc.creatorQu, Yen_US
dc.creatorZhang, Ken_US
dc.creatorShang, Len_US
dc.creatorLiang, Pen_US
dc.creatorChen, Fen_US
dc.creatorTang, Xen_US
dc.creatorLuo, Wen_US
dc.creatorChin, LKen_US
dc.creatorFeng, Sen_US
dc.creatorLi, Ben_US
dc.date.accessioned2026-01-22T09:20:33Z-
dc.date.available2026-01-22T09:20:33Z-
dc.identifier.urihttp://hdl.handle.net/10397/117016-
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.rights© 2025 American Chemical Societyen_US
dc.rightsThis document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Sensors, copyright © 2025 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acssensors.4c02417.en_US
dc.subjectLaser-induced forward transferen_US
dc.subjectMicroporesen_US
dc.subjectRNA sequencingen_US
dc.subjectSingle-cell analysisen_US
dc.subjectSingle-cell sortingen_US
dc.titleAutomated laser-assisted single-cell sorting for cell functional and RNA sequencingen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage846en_US
dc.identifier.epage856en_US
dc.identifier.volume10en_US
dc.identifier.issue2en_US
dc.identifier.doi10.1021/acssensors.4c02417en_US
dcterms.abstractAccurate and efficient sorting of single target cells is crucial for downstream single-cell analysis, such as RNA sequencing, to uncover cellular heterogeneity and functional characteristics. However, conventional single-cell sorting techniques, such as manual micromanipulation or fluorescence-activated cell sorting, do not match current demands and are limited by low throughput, low sorting efficiency and precision, or limited cell viability. Here, we report an automated, highly efficient single-cell sorter, integrating laser-induced forward transfer (LIFT) with a high-throughput picoliter micropore array. The micropore array was surface-functionalized to manipulate liquid surface tension, facilitating the formation of single-cell picoliter droplets in the micropores to realize automated and highly efficient (>80%) single-cell isolation. Using an in-house built microscopic system, rare target cells were identified and automatically retrieved by LIFT with precise sorting efficiency (about 100%) for downstream single-cell analysis while maintaining high cell viability (about 80%). As a case demonstration, we demonstrated the accurate sorting of rare transfected PC-9 cells and post-transfection cell culture, minimizing cell loss and the risk of contamination. Furthermore, we performed single-cell RNA sequencing and showed that high-quality single-cell transcriptome information was efficiently and reliably obtained during cell sorting, preventing additional costs due to low sorting accuracy. The single-cell sorter will become invaluable for single-cell analysis, laying the foundation for multiomics analysis and precision medicine research.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationACS sensors, 28 Feb. 2025, v. 10, no. 2, p. 846-856en_US
dcterms.isPartOfACS sensorsen_US
dcterms.issued2025-02-28-
dc.identifier.scopus2-s2.0-86000373794-
dc.identifier.pmid39843241-
dc.identifier.eissn2379-3694en_US
dc.description.validate202601 bcchen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.SubFormIDG000728/2025-12-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThe work was supported by the National Natural Science Foundation of China (Grant No. 62104227).en_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryGreen (AAM)en_US
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