| Literature DB >> 26192270 |
Maureen McKeague1, Annalisa De Girolamo2, Stefania Valenzano2, Michelangelo Pascale2, Annamaria Ruscito3, Ranganathan Velu3, Nadine R Frost3, Kayla Hill3, McKenzie Smith3, Erin M McConnell3, Maria C DeRosa3.
Abstract
Nucleic acid aptamers are versatile molecular recognition agents that bind to their targets with high selectivity and affinity. The past few years have seen a dramatic increase in aptamer development and interest for diagnostic and therapeutic applications. As the applications for aptamers expand, the need for a more standardized, stringent, and informative characterization and validation methodology increases. Here we performed a comprehensive analysis of a panel of conventional affinity binding assays using a suite of aptamers for the small molecule target ochratoxin A (OTA). Our results highlight inconsistency between conventional affinity assays and the need for multiple characterization strategies. To mitigate some of the challenges revealed in our head-to-head comparison of aptamer binding assays, we further developed and evaluated a set of novel strategies that facilitate efficient screening and characterization of aptamers in solution. Finally, we provide a workflow that permits rapid and robust screening, characterization, and functional verification of aptamers thus improving their development and integration into novel applications.Entities:
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Year: 2015 PMID: 26192270 DOI: 10.1021/acs.analchem.5b02102
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986