Literature DB >> 15780713

Immuno-PCR: high sensitivity detection of proteins by nucleic acid amplification.

Christof M Niemeyer1, Michael Adler, Ron Wacker.   

Abstract

Nucleic acid amplification techniques are used for signal generation in antibody-based immunoassays, thereby dramatically enhancing the sensitivity of conventional immunoassays. Methodological aspects, as well as applications of this novel approach, are summarized in this review, with an emphasis on immuno-polymerase chain reaction (IPCR). IPCR is based on chimeric conjugates of specific antibodies and nucleic acid molecules, the latter of which are used as markers to be amplified by PCR for signal generation. The enormous efficiency of nucleic acid amplification typically leads to a 100-10,000-fold increase in sensitivity, as compared with the analogous enzyme-amplified immunoassay. The evolution of IPCR included the development of efficient reagents, the design of assay formats and the maintenance of functionality, even within complex biological matrices. Eventually, IPCR crossed the border from being a research method to a routine laboratory technique, enabling a broad range of applications in immunological research and clinical diagnostics.

Mesh:

Year:  2005        PMID: 15780713     DOI: 10.1016/j.tibtech.2005.02.006

Source DB:  PubMed          Journal:  Trends Biotechnol        ISSN: 0167-7799            Impact factor:   19.536


  52 in total

1.  Immuno-PCR for the early serological diagnosis of acute infectious diseases: the Q fever paradigm.

Authors:  N Malou; A Renvoise; C Nappez; D Raoult
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2012-01-10       Impact factor: 3.267

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Journal:  Biomicrofluidics       Date:  2015-12-08       Impact factor: 2.800

Review 3.  The Past, Present, and (Possible) Future of Serologic Testing for Lyme Disease.

Authors:  Elitza S Theel
Journal:  J Clin Microbiol       Date:  2016-02-10       Impact factor: 5.948

4.  Multiplexed aptasensing of food contaminants by using terminal deoxynucleotidyl transferase-produced primer-triggered rolling circle amplification: application to the colorimetric determination of enrofloxacin, lead (II), Escherichia coli O157:H7 and tropomyosin.

Authors:  Yumei Du; Yangyang Zhou; Yanli Wen; Xiaojun Bian; Yuanyuan Xie; Weijia Zhang; Gang Liu; Juan Yan
Journal:  Mikrochim Acta       Date:  2019-11-25       Impact factor: 5.833

5.  Antibody-based enrichment of peptides on magnetic beads for mass-spectrometry-based quantification of serum biomarkers.

Authors:  Jeffrey R Whiteaker; Lei Zhao; Heidi Y Zhang; Li-Chia Feng; Brian D Piening; Leigh Anderson; Amanda G Paulovich
Journal:  Anal Biochem       Date:  2006-12-20       Impact factor: 3.365

6.  DNA-encoded antibody libraries: a unified platform for multiplexed cell sorting and detection of genes and proteins.

Authors:  Ryan C Bailey; Gabriel A Kwong; Caius G Radu; Owen N Witte; James R Heath
Journal:  J Am Chem Soc       Date:  2007-01-30       Impact factor: 15.419

7.  Protein detection via direct enzymatic amplification of short DNA aptamers.

Authors:  Nicholas O Fischer; Theodore M Tarasow; Jeffrey B-H Tok
Journal:  Anal Biochem       Date:  2007-10-01       Impact factor: 3.365

8.  Real-time PCR detection of protein analytes with conformation-switching aptamers.

Authors:  Litao Yang; Andrew D Ellington
Journal:  Anal Biochem       Date:  2008-05-20       Impact factor: 3.365

9.  Microarray-based multiplexed scanometric immunoassay for protein cancer markers using gold nanoparticle probes.

Authors:  Dongwoo Kim; Weston L Daniel; Chad A Mirkin
Journal:  Anal Chem       Date:  2009-11-01       Impact factor: 6.986

10.  DNAzyme-based probes for telomerase detection in early-stage cancer diagnosis.

Authors:  Hui Wang; Michael J Donovan; Ling Meng; Zilong Zhao; Youngmi Kim; Mao Ye; Weihong Tan
Journal:  Chemistry       Date:  2013-02-20       Impact factor: 5.236

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