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Aptamer decorated PDA@magnetic silica microparticles for bacteria purification

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journal contribution
posted on 2024-07-10, 09:34 authored by Murat Kavruk, Zahra Babaie, Güneş Kibar, Barbaros Çetin, Hasan Yeşilkaya, Yassine Amrani, Ali Doğan Dursun, V Cengiz Özalp

One significant constraint in the advancement of biosensors is the signal-to-noise ratio, which is adversely affected by the presence of interfering factors such as blood in the sample matrix. In the present investigation, a specific aptamer binding was chosen for its affinity, while exhibiting no binding affinity towards non-target bacterial cells. This selective binding property was leveraged to facilitate the production of magnetic microparticles decorated with aptamers. A novel assay was developed to effectively isolate S. pneumoniae from PBS or directly from blood samples using an aptamer with an affinity constant of 72.8 nM. The capture experiments demonstrated efficiencies up to 87% and 66% are achievable for isolating spiked S. pneumoniae in 1 mL PBS and blood samples, respectively. Graphical abstract

Funding

Katip Çelebi-Newton Fund Industry Academy Partnership Program of the Scientific and Technical Research Council of Türkiye

Royal Academy of Engineering Grant No. 220N316

History

Citation

Kavruk, M., Babaie, Z., Kibar, G. et al. Aptamer decorated PDA@magnetic silica microparticles for bacteria purification. Microchim Acta 191, 285 (2024). https://doi.org/10.1007/s00604-024-06322-3

Author affiliation

College of Life Sciences, Respiratory Sciences

Version

  • VoR (Version of Record)

Published in

Microchimica Acta

Volume

191

Issue

5

Pagination

285

Publisher

Springer Science and Business Media LLC

issn

0026-3672

eissn

1436-5073

Acceptance date

2024-03-20

Copyright date

2024

Available date

2024-07-10

Language

en

Deposited by

Dr Hasan Yesilkaya

Deposit date

2024-07-09

Data Access Statement

The data set used and analyzed during the current study are available from the corresponding author on reasonable request.

Rights Retention Statement

  • No

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