Publication:
CRISPR-on-chip for point-of-care diagnostics

dc.contributor.departmentKUTTAM (Koç University Research Center for Translational Medicine)
dc.contributor.departmentKUIS AI (Koç University & İş Bank Artificial Intelligence Center)
dc.contributor.departmentDepartment of Mechanical Engineering
dc.contributor.departmentSchool of Medicine
dc.contributor.departmentKUAR (KU Arçelik Research Center for Creative Industries)
dc.contributor.departmentGraduate School of Sciences and Engineering
dc.contributor.kuauthorAtçeken, Nazente
dc.contributor.kuauthorYığcı, Defne
dc.contributor.kuauthorTaşoğlu, Savaş
dc.contributor.kuauthorKahya, Alptekin
dc.contributor.schoolcollegeinstituteResearch Center
dc.contributor.schoolcollegeinstituteCollege of Engineering
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.contributor.schoolcollegeinstituteGRADUATE SCHOOL OF SCIENCES AND ENGINEERING
dc.date.accessioned2026-02-26T07:11:26Z
dc.date.available2026-02-25
dc.date.issued2026
dc.description.abstractCRISPR-based diagnostic platforms have gained significant momentum in recent years, enabling highly sensitive and specific detection of pathogens and diseases. Due to their practical benefits, these platforms have become widely adopted in point-of-care (PoC) applications. CRISPR-on-chip technology integrates CRISPR-Cas platforms with diverse microfluidic systems, allowing scalability and portable, real-time, and precise biomolecule detection. This approach enhances diagnostic accuracy, reduces processing times, and minimizes the need for complex laboratory infrastructures, unlike in conventional diagnostics. Using CRISPR-Cas enzymes in microfluidic systems, CRISPR-on-chip platforms offer key advantages such as single-molecule sensitivity, multiplex detection, and applicability. However, integration with microfluidics for PoC applications is still poorly understood, despite CRISPR-Cas being widely used. This study reviews recent developments in CRISPR-on-chip-based diagnostics and highlights its potential applications in infectious diseases, biosensors, and personalized medicine. Furthermore, challenges and future perspectives in achieving an ideal diagnostic solution are discussed.
dc.description.fulltextYes
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessGold OA
dc.description.openaccessGreen OA
dc.description.peerreviewstatusN/A
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuTÜBİTAK
dc.description.sponsorshipS.T. acknowledges TUBITAK 2232 International Fellowship for Outstanding Researchers Award (118C391), TUBITAK-1001 Scientific and Technological Research Projects (123S582, 123Z050, 225S122, 125Z215), Alexander von Humboldt Research Fellowship for Experienced Researchers, Marie Sk & lstrok;odowska-Curie Individual Fellowship (101003361), and Royal Academy Newton-Katip Celebi Transforming Systems Through Partnership Award (120N019) for the financial support of this research. N.A. acknowledges support by EMBO Scientific Exchange Grant (11627) and TUBITAK-2218 Domestic Postdoctoral Research Scholarship Project (122C195). Opinions, interpretations, conclusions, and recommendations are those of the author and are not necessarily endorsed by the TUBITAK. This work was partially supported by the Science Academy's Young Scientist Awards Program (BAGEP), Outstanding Young Scientists Awards (GEBIP), Dr. Nejat Eczacibasi Medicine Incentive Award, IBG Science Medal from Izmir Biomedicine and Genome Center, ELGINKAN Foundation Technology Prize, TGC Sedat Simavi Health Sciences Award, Parlar Foundation Research Incentive Award, Parlar Foundation Technology Incentive Award, and Bilim Kahramanlari Dernegi The Young Scientist Award. This study was conducted using the service and infrastructure of Koc University Translational Medicine Research Center (KUTTAM). The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed. Illustrations from the Figures were used from BioRender.com.
dc.description.versionN/A
dc.identifier.doi10.1021/acsnano.5c19771
dc.identifier.eissn1936-086X
dc.identifier.embargoNo
dc.identifier.endpage2577
dc.identifier.grantno118C391
dc.identifier.grantno101003361
dc.identifier.issn1936-0851
dc.identifier.issue3
dc.identifier.pubmed41527500
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-105028700128
dc.identifier.startpage2561
dc.identifier.urihttps://doi.org/10.1021/acsnano.5c19771
dc.identifier.urihttps://hdl.handle.net/20.500.14288/32401
dc.identifier.volume20
dc.identifier.wos001661052200001
dc.keywordsCRISPR-based diagnostic
dc.keywordsMicrofluidics
dc.keywordsPoint-of-care (PoC)
dc.keywordsCRISPR-on-chip technology
dc.language.isoeng
dc.publisherAmerican Chemical Society
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofACS Nano
dc.relation.openaccessYes
dc.rightsCC BY-NC-ND (Attribution-NonCommercial-NoDerivs)
dc.rights.uriAttribution, Non-commercial, No Derivative Works (CC-BY-NC-ND)
dc.subjectChemistry
dc.subjectScience and technology
dc.subjectMaterials science
dc.titleCRISPR-on-chip for point-of-care diagnostics
dc.typeReview
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