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A simple and sensitive detection of small molecule-protein interactions based on terminal protection-mediated exponential strand displacement amplification
- Source :
- The Analyst. 143(9)
- Publication Year :
- 2018
-
Abstract
- We herein describe a simple and sensitive strategy to detect a small molecule-protein interaction based on terminal protection-mediated exponential strand displacement amplification (eSDA). In principle, the small molecule linked to a DNA probe protects the DNA probe against the exonuclease I-catalyzed degradation after its binding to the corresponding target protein. The protected DNA probe then serves as a template to promote eSDA. Consequently, a large number of duplexes are produced, which leads to a high fluorescence from a double-stranded DNA specific fluorescent dye, SYBR Green I. As a model system to prove this sensing strategy, the interaction between biotin and streptavidin (SA), which is known to be the strongest among the non-covalent biological interactions, was selected and its analytical performance was thoroughly investigated. As a result, SA was sensitively detected with the limit of detection of 16 pM. In addition, the practical applicability of this method was successfully demonstrated by reliably determining the SA in human serum.
- Subjects :
- Streptavidin
Exonuclease
Biotin
02 engineering and technology
Diamines
010402 general chemistry
01 natural sciences
Biochemistry
Analytical Chemistry
chemistry.chemical_compound
Limit of Detection
Electrochemistry
Environmental Chemistry
Humans
A-DNA
Benzothiazoles
Organic Chemicals
Spectroscopy
biology
Hybridization probe
Multiple displacement amplification
Proteins
Nucleic acid amplification technique
DNA
021001 nanoscience & nanotechnology
Small molecule
0104 chemical sciences
chemistry
SYBR Green I
Biophysics
biology.protein
Quinolines
0210 nano-technology
DNA Probes
Nucleic Acid Amplification Techniques
Subjects
Details
- ISSN :
- 13645528
- Volume :
- 143
- Issue :
- 9
- Database :
- OpenAIRE
- Journal :
- The Analyst
- Accession number :
- edsair.doi.dedup.....7deffd2228b100f168b4b5e59d4de716