Nonantibody-based recognition: alternative molecules for detection of pathogens

被引:47
作者
Ngundi, Miriam M.
Kulagina, Nodezhda V.
Anderson, George P.
Taitt, Chris R.
机构
[1] USN, Res Lab, Ctr Biomol Sci & Engn, Washington, DC 20375 USA
[2] Covance, Vienna, VA 22182 USA
[3] US FDA, Bethesda, MD 20892 USA
关键词
alternative recognition; antimicrobial peptide; aptamer; cell-based assays; combinatorial carbohydrate; combinatorial peptide; detection; molecular imprinting; phage display; receptor-based assays;
D O I
10.1586/14789450.3.5.511
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Immunoassays have been well established for many years as the cornerstone of detection technologies. These assays are sensitive, selective and, in general, highly resistant to interference from complex sample matrices when compared with nucleic acid-based tests. However, both antibody- and nucleic acid-based detection systems require a priori knowledge of the target and development of specific reagents; multiplexed assays con become increasingly problematic when attempting to detect a plethora of different targets, the identities of which are unknown. In an effort to circumvent many of the limitations inherent in these conventional assays, other recognition reagents are being explored as alternatives, or indeed as adjuncts, to antibodies for pathogen and toxin detection. This article will review a number of different recognition systems ranging in complexity from small molecules, such as nucleic-acid aptamers, carbohydrates and peptides, to systems as highly complicated as whole cells and organisms. All of these alternative systems have tremendous potential to achieve superior sensitivity, selectivity, and stability, but are also subject to their own limitations, which are also discussed. In short, while in its infancy, this field holds great promise for the development of rapid, fieldable assays that are highly complementary to existing antibody- and nucleic acid-based technologies.
引用
收藏
页码:511 / 524
页数:14
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