| Literature DB >> 26003883 |
Ghamar Soltan Dorraj1, Mohammad Javad Rassaee2, Ali Mohammad Latifi3, Bahram Pishgoo4, Mahmood Tavallaei5.
Abstract
Troponin T and I are ideal markers which are highly sensitive and specific for myocardial injury and have shown better efficacy than earlier markers. Since aptamers are ssDNA or RNA that bind to a wide variety of target molecules, the purpose of this research was to select an aptamer from a 79bp single-stranded DNA (ssDNA) random library that was used to bind the Human Cardiac Troponin I from a synthetic nucleic acids library by systematic evolution of ligands exponential enrichment (Selex) based on several selection and amplification steps. Human Cardiac Troponin I protein was coated onto the surface of streptavidin magnetic beads to extract specific aptamer from a large and diverse random ssDNA initial oligonucleotide library. As a result, several aptamers were selected and further examined for binding affinity and specificity. Finally TnIApt 23 showed beast affinity in nanomolar range (2.69nM) toward the target protein. A simple and rapid colorimetric detection assay for Human Cardiac Troponin I using the novel and specific aptamer-AuNPs conjugates based on dot blot assay was developed. The detection limit for this protein using aptamer-AuNPs-based assay was found to be 5ng/ml.Entities:
Keywords: DNA aptamer; Dot blot assay; Gold nanoparticle; Human Cardiac Troponin I; Selex
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Year: 2015 PMID: 26003883 DOI: 10.1016/j.jbiotec.2015.05.002
Source DB: PubMed Journal: J Biotechnol ISSN: 0168-1656 Impact factor: 3.307