Evidence map›Paper›PMID 40190823›Full record

ArticleResearch in pharmaceutical sciences2025

A novel hybrid approach to overcome defects of CE-SELEX and cell-SELEX in developing aptamers against aspartate β-hydroxylase.

Hadi Bakhtiari, Hamed Naghoosi, Sina Sattari, Mahmoud Vahidi, Mehdi Shakouri Khomartash, Ali Faridfar, Mohsen Rajaeinejad, Mohsen Nikandish

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Article in Research in pharmaceutical sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

8 authors.

Hadi BakhtiariCancer Epidemiology Research Center (AJA-CERTC), Aja University of Medical Sciences, Tehran, Iran.
Hamed NaghoosiInfectious Diseases Research Center, Aja University of Medical Sciences, Tehran, Iran.
Sina SattariHealth Research Center, Shahid Chamran Hospital, Tehran, Iran.
Mahmoud VahidiMedical Biotechnology Research Center, Aja University of Medical Sciences, Tehran, Iran.
Mehdi Shakouri KhomartashMedical Biotechnology Research Center, Aja University of Medical Sciences, Tehran, Iran.
Ali FaridfarCancer Epidemiology Research Center (AJA-CERTC), Aja University of Medical Sciences, Tehran, Iran.
Mohsen RajaeinejadCancer Epidemiology Research Center (AJA-CERTC), Aja University of Medical Sciences, Tehran, Iran.
Mohsen NikandishCancer Epidemiology Research Center (AJA-CERTC), Aja University of Medical Sciences, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and purpose: Aptamers, a new category of molecular probes, are overthrowing antibodies in molecular diagnostics. However, there are serious problems with using aptamers for this application including poor or non-specific binding Experimental approach: In our approach, the selected oligomer pool from the last cycle of CE-SELEX was sequenced and then subjected to 3 additional rounds of Cell-SELEX which provides native ASPH (CEC hybrid-SELEX). High-throughput sequencing was applied to achieve a comprehensive sight of the enriched pools. Further confirmatory investigations on oligomers with higher copy numbers were performed using flow cytometry. Findings/Results: Three selected oligomers, AP-CEC 1, AP-CEC 2, and AP-CEC 3, showing Kd values of 43.09 nM, 34.85 nM, and 35.92 nM, respectively, were achieved based on the affinity assessment of the ASPH-expressing cells. Conclusion and implications: Our research suggested that CEC hybrid-SELEX could help recognize which oligomers from CE-SELEX are more capable of binding native ASPH

Indexed as

AptamersAspartate β-hydroxylaseCapillary electrophoresisHigh-throughput nucleotide sequencingSELEX aptamer technique

Identifiers

PMID40190823
PMCPMC11972023

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