Title :
Comparison of fluorophore and peroxidase labeled aptamer assays for MUC1 detection in cancer cells
Author :
Flanagan, S. ; Limson, J. ; Fogel, R.
Author_Institution :
Biotechnol. Innovation Centre, Rhodes Univ., Grahamstown, South Africa
Abstract :
Aptamers hold great promise for cancer diagnosis and therapy. Several biosensors incorporate aptamers as biorecognition elements for tumor markers although few evaluate their detection in a native conformation and cellular micro-environment. In this study, fluorophore and peroxidase labeled aptamer configurations were compared for the detection of MCF7 breast and SW620 colon cancer cell lines expressing the tumor marker MUC1. Fluorescence based detection showed selective binding to the cell lines relative to a nonbinding control sequence with sequence specific binding differences between MUC1 aptamers accredited to variation in the glycosylation state of expressed MUC1. The peroxidase labeled assay showed high detection sensitivity although low binding specificity was observed for the MUC1 aptamers to the cell lines. Results suggest that aptamers susceptible to non specific binding to cells may limit the applicability of enzymatic amplification to improve aptasensor sensitivity.
Keywords :
biochemistry; biosensors; cancer; cellular biophysics; chemical sensors; enzymes; fluorescence; molecular biophysics; patient diagnosis; tumours; MCF7 breast cancer cell line detection; SW620 colon cancer cell line detection; aptasensor sensitivity; biorecognition elements; biosensors; cellular microenvironment; enzymatic amplification; fluorescence based detection; fluorophore labeled aptamer assays; glycosylation state; nonbinding control sequence; peroxidase labeled aptamer assays; tumor marker MUC1 detection; Biosensors; Cancer; Cells (biology); Dairy products; Fluorescence; Powders; Tumors; Aptamer; MCF7; MUC1; SW620; biosensor platform; enzyme linked oligonucleotide assay; fluorescence assay;
Conference_Titel :
Biomedical Circuits and Systems Conference (BioCAS), 2014 IEEE
Conference_Location :
Lausanne
DOI :
10.1109/BioCAS.2014.6981720