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E-DNA scaffold sensors and the reagentless, single- step, measurement of HIV-diagnostic antibodies in human serum

Microsystems & Nanoengineering 2020年第1期6卷 1141-1148页

作者： claudio parolo Ava S.Greenwood Nathan E.Ogden Di Kang Chase Hawes Gabriel Ortega Netzahualcoyotl Arroyo-Curras Kevin W.Plaxco Department of Chemistry and Biochemistry University of CaliforniaSanta BarbaraSanta BarbaraCAUSA Department of Materials University of CaliforniaSanta BarbaraSanta BarbaraCAUSA Department of Pharmacology and Molecular Sciences Johns Hopkins School of MedicineBaltimoreMD 21205USA Interdepartmental Program in Biomolecular Science and Engineering University of CaliforniaSanta BarbaraSanta BarbaraCA 93106USA

The multiplexed,point-of-care measurement of specific antibodies could improve the speed with which diseases are diagnosed and their treatment *** this end,we are developing E-DNA scaffold sensors,which consist of a rigid,nucleic acid“scaffold”attached on one end to an electrode and presenting both a redox reporter and an epitope on the *** the absence of antibody,the reporter efficiently transfers electrons when interrogated ***-induced steric hindrance limits movement,reducing electron transfer in a manner that is both easily measured and quantitatively related to target *** we have used monoclonal antibodies to explore the analytical performance of E-DNA sensors,showing that they support the rapid,single-step,quantitative detection of multiple antibodies in small volume ***,in contrast,we employ authentic human samples to better explore the platform’s clinical ***,we developed E-DNA sensors targeting three HIV-specific antibodies and then compared the analytical and clinical performance of these against those of gold standard serological *** so we find that,although the multistep amplification of an ELISA leads to a lower detection limits,the clinical sensitivity of ELISAs,E-DNA sensors and lateral-flow dipsticks are indistinguishable across our test *** thus appears that,by merging the quantitation and multiplexing of ELISAs with the convenience and speed of dipsticks,E-DNA scaffold sensors could significantly improve on current serological practice.

关键词： antibodies attached initiated

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