A simple and sensitive detection of small molecule–protein interactions based on terminal protection-mediated exponential strand displacement amplification
Literature Information
Chang Yeol Lee, Hyo Yong Kim, Soeun Kim, Ki Soo Park, Hyun Gyu Park
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.
Related Literature
Structural and redox properties of VOx and Pd/VOx thin film model catalysts studied by TEM and SAED
Simon Penner, Bernhard Klötzer, Bernd Jenewein
DOI: 10.1039/B700650K
Compositional analysis of copper–silica precipitation tubes
Jason J. Pagano, Stephanie Thouvenel-Romans, Oliver Steinbock
DOI: 10.1039/B612982J
Gold catalysts for pure hydrogen production in the water–gas shift reaction: activity, structure and reaction mechanism
DOI: 10.1039/B607837K
Adiabatic and non-adiabatic corrections to rovibrational energies of diatomic molecules: variational calculations with experimental accuracy
DOI: 10.1039/B700044H
Photocatalytic properties of titania nanostructured films fabricated from titania nanosheets
Tatsuo Shibata, Nobuyuki Sakai, Katsutoshi Fukuda, Yasuo Ebina, Takayoshi Sasaki
DOI: 10.1039/B618448K
Theoretical and experimental determination of the electronic structure of V2O5, reduced V2O5−x and sodium intercalated NaV2O5
Stefan Laubach, Peter C. Schmidt, Andreas Thißen, Francisco Javier Fernandez-Madrigal, Qi-Hui Wu, Wolfram Jaegermann, Matthias Klemm, Siegfried Horn
DOI: 10.1039/B612489E
Inelastic insights for molecular tunneling pathways: Bypassing the terminal groups
Alessandro Troisi, Mark A. Ratner
DOI: 10.1039/B702377D
You might also like
What is the market or research trend for N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0)?
N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0) is increasingly being used ...
What precautions should be taken when handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate (CAS: 1050507-06-6)?
When handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate, appropriate p...
What regulatory guidelines apply to diethyldiselane (CAS: 628-39-7)?
Diethyldiselane (CAS: 628-39-7) is classified under the Globally Harmonized Syst...
What is the market or research trend for oxocopper (CAS: 12053-18-8)?
The market for oxocopper (CAS: 12053-18-8) is primarily driven by its use in cat...
What is the market or research trend for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-carboxylic acid?
The market for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-c...
What is 2-(1-Pyrrolidinyl)-4-pyridinamine (CAS: 35981-63-6)?
2-(1-Pyrrolidinyl)-4-pyridinamine is a chemical compound with the CAS number 359...
What are the physical and chemical properties of 2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1)?
2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1) is a crystalline sol...
How is (S)-Alpha-allyl-proline hydrochloride (CAS: 129704-91-2) typically synthesized?
(S)-Alpha-allyl-proline hydrochloride is usually synthesized via a Wittig reacti...
What is 3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5)?
3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5) is an organic compound w...
How is Lys-SMCC-DM1 (CAS: 1281816-04-3) typically synthesized?
Lys-SMCC-DM1 is synthesized via a multi-step process involving the coupling of S...
Source Journal
Analyst

Analyst publishes analytical and bioanalytical research that reports premier fundamental discoveries and inventions, and the applications of those discoveries, unconfined by traditional discipline barriers.










![N-{15-[(2,5-Dioxo-1-pyrrolidinyl)oxy]-15-oxo-3,6,9,12-tetraoxapentadec-1-yl}-2-(2-propyn-1-yloxy)acetamide structure N-{15-[(2,5-Dioxo-1-pyrrolidinyl)oxy]-15-oxo-3,6,9,12-tetraoxapentadec-1-yl}-2-(2-propyn-1-yloxy)acetamide structure](https://static.chemtradehub.com/structs/210/2101206-92-0-2eb5.webp)



