Literature DB >> 32624754

Ultrasensitive SPR detection of miRNA-93 using antibody-enhanced and enzymatic signal amplification.

Stefan Schmieder1, Janek Weißpflog1, Norbert Danz2, Max Hübner3,4, Simone Kreth3,4, Udo Klotzbach1, Frank Sonntag1.   

Abstract

MiRNAs are endogenous noncoding RNA molecules. They play important gene-regulatory roles by binding to the mRNA of target genes thereby leading to either transcript degradation or translational repression. In virtually all diseases, distinct alterations of miRNA expression profiles have been found thus suggesting miRNAs as interesting biomarkers. Here, we present an SPR biosensor that utilizes disposable, injection-molded sensor chip/microfluidic hybrids combined with a lateral imaging optical system for parallel analysis of three one-dimensional spot arrays to detect miRNA-93. To increase the sensitivity of the biosensor we used two different amplification strategies. By adding an RNA-DNA-hybrid antibody for primary signal amplification, a limit of detection of 10 pmol/L was achieved. Based on that method we demonstrate the detection of miRNA-93 in total RNA lysate from HEK-293 cells. Utilizing an enzymatic signal amplification with Poly(A) polymerase, the sensitivity could be increased even further leading to a limit of detection of 1 fmol/L.
© 2017 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  Biochip; Molecular diagnostics; SPR; Surface plasmon resonance; miRNA

Year:  2017        PMID: 32624754      PMCID: PMC6999304          DOI: 10.1002/elsc.201700104

Source DB:  PubMed          Journal:  Eng Life Sci        ISSN: 1618-0240            Impact factor:   2.678


  1 in total

1.  DNA walking system integrated with enzymatic cleavage reaction for sensitive surface plasmon resonance detection of miRNA.

Authors:  Sijia Chen; Yuhan He; Lin Liu; Jianxiu Wang; Xinyao Yi
Journal:  Sci Rep       Date:  2022-09-27       Impact factor: 4.996

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.