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Sequence-constructive SELEX: a new strategy for screening DNA aptamer binding to Globo H
Chin-Yu Wang1, Chung-Yi Wu1, Ting-Chun Hung1
1Genomics Research Center, Academia Sinica, 128 Academia Road, Sec. 2, Nankang, Taipei 11529, Taiwan.
Biochemical and Biophysical Research Communications
|August 28, 2014
Summary
Researchers developed DNA aptamers targeting Globo H, a tumor antigen, using a novel stepwise SELEX method. This approach enhanced aptamer binding affinity and selectivity for cancer biomarker detection.
Area of Science:
- Biochemistry
- Molecular Biology
- Biotechnology
Background:
- Globo H is a significant tumor-associated carbohydrate antigen.
- Developing specific recognition agents for Globo H is crucial for cancer diagnostics.
Purpose of the Study:
- To develop DNA aptamers with high affinity and specificity for Globo H.
- To employ a novel stepwise sequence-constructive SELEX method for aptamer development.
Main Methods:
- Utilized a stepwise sequence-constructive SELEX (Systematic Evolution of Ligands by Exponential Enrichment) method.
- Initiated SELEX with a 15-base randomized DNA library.
- Iteratively extended and randomized DNA sequences over three rounds of SELEX.
Main Results:
- The sequence-constructive SELEX approach enhanced the binding affinity of DNA aptamers to Globo H.
- Developed DNA aptamers demonstrated high selectivity, distinguishing Globo H from related structures.
- The aptamers successfully discriminated between various glycans based on structural differences.
Conclusions:
- The novel stepwise sequence-constructive SELEX method is effective for developing high-affinity and specific DNA aptamers.
- These aptamers show potential as diagnostic tools for recognizing the Globo H tumor antigen.
- The study highlights the capability of aptamers in glycan structure discrimination for cancer biomarker applications.
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