Bioelectronic sensor technology for detection of cystic fibrosis and hereditary hemochromatosis mutations
| Autor: | Timothy T. Stenzel, Karla J. Matteson, Daniel H. Farkas, Karen Snow Bailey, Kristin G. Monaghan, Jeanne C. Beck, Susan H. Bernacki, Frederick V. Schaefer, Antony E. Shrimpton, Vivian Chan, Yenbou Liu, Victoria M. Pratt, Michael J. Friez, Wenmei Shi |
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| Rok vydání: | 2003 |
| Předmět: |
Cystic Fibrosis
Genotype DNA Mutational Analysis Cystic Fibrosis Transmembrane Conductance Regulator Computational biology Biosensing Techniques Biology Bioinformatics Cystic fibrosis Pathology and Forensic Medicine Cftr gene chemistry.chemical_compound medicine Humans Biochip Hemochromatosis Protein Cell Line Transformed Oligonucleotide Array Sequence Analysis Base Sequence Molecular genetic testing Histocompatibility Antigens Class I Membrane Proteins General Medicine medicine.disease Blood lymphocyte Medical Laboratory Technology chemistry Hereditary hemochromatosis Hemochromatosis Electronics DNA Biotechnology |
| Zdroj: | Archives of pathologylaboratory medicine. 127(12) |
| ISSN: | 1543-2165 |
| Popis: | Context.—Bioelectronic sensors, which combine microchip and biological components, are an emerging technology in clinical diagnostic testing. An electronic detection platform using DNA biochip technology (eSensor) is under development for molecular diagnostic applications. Owing to the novelty of these devices, demonstrations of their successful use in practical diagnostic applications are limited. Objective.—To assess the performance of the eSensor bioelectronic method in the validation of 6 Epstein-Barr virus–transformed blood lymphocyte cell lines with clinically important mutations for use as sources of genetic material for positive controls in clinical molecular genetic testing. Two cell lines carry mutations in the CFTR gene (cystic fibrosis), and 4 carry mutations in the HFE gene (hereditary hemochromatosis). Design.—Samples from each cell line were sent for genotype determination to 6 different molecular genetic testing facilities, including the laboratory developing the DNA biochips. In addition to the bioelectronic method, at least 3 different molecular diagnostic methods were used in the analysis of each cell line. Detailed data were collected from the DNA biochip output, and the genetic results were compared with those obtained using the more established methods. Results.—We report the successful use of 2 applications of the bioelectronic platform, one for detection of CFTR mutations and the other for detection of HFE mutations. In all cases, the results obtained with the DNA biochip were in concordance with those reported for the other methods. Electronic signal output from the DNA biochips clearly differentiated between mutated and wild-type alleles. This is the first report of the use of the cystic fibrosis detection platform. Conclusions.—Bioelectronic sensors for the detection of disease-causing mutations performed well when used in a “real-life” situation, in this case, a validation study of positive control blood lymphocyte cell lines with mutations of public health importance. This study illustrates the practical potential of emerging bioelectronic DNA detection technologies for use in current molecular diagnostic applications. |
| Databáze: | OpenAIRE |
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