4.7 Article

Hybrid Aptamer-Molecularly Imprinted Polymer (aptaMIP) Nanoparticles from Protein Recognition-A Trypsin Model

期刊

MACROMOLECULAR BIOSCIENCE
卷 21, 期 5, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/mabi.202100002

关键词

aptamers; molecularly imprinted polymers; nanoparticles; protein; solid‐ phase synthesis

资金

  1. EPSRC [EP/K015095/1, EP/S003339/1]
  2. EPSRC [EP/S003339/1, EP/K015095/1] Funding Source: UKRI

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The research shows that by slightly adapting the chemical structure of a DNA aptamer and incorporating it into the recognition part of a MIP, an aptamer-MIP hybrid or aptaMIP is created, which is effective for detecting the target protein trypsin. AptaMIP nanoparticles demonstrate superior binding affinity and detection sensitivity compared to conventional MIP nanoparticles, while also showing good selectivity against other protein targets. Introducing the aptamer as a macro-monomer into the MIP scaffold has beneficial effects and potential for significant improvement in this class of polymers.
Aptamers offer excellent potential for replacing antibodies for molecular recognition purposes however their performance can compromise with biological/environmental degradation being a particular problem. Molecularly imprinted Polymers (MIPs) offer an alternative to biological materials and while these offer the robustness and ability to work in extreme environmental conditions, they often lack the same recognition performance. By slightly adapting the chemical structure of a DNA aptamer it is incorporated for use as the recognition part of a MIP, thus creating an aptamer-MIP hybrid or aptaMIP. Here these are developed for the detection of the target protein trypsin. The aptaMIP nanoparticles offer superior binding affinity over conventional MIP nanoparticles (nanoMIPs), with K-D values of 6.8 x 10(-9) (+/- 0.2 x 10(-9)) m and 12.3 x 10(-9) (+/- 0.4 x 10(-9)) m for the aptaMIP and nanoMIP, respectively. The aptaMIP also outperforms the aptamer only (10.3 x 10(-9) m). Good selectivity against other protein targets is observed. Using surface plasmon resonance, the limit of detection for aptaMIP nanoparticles is twofold lower (2 nm) compared to the nanoMIP (4 nm). Introduction of the aptamer as a macro-monomer into the MIP scaffold has beneficial effects and offers potential to improve this class of polymers significantly.

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