کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
867621 | 1470992 | 2011 | 4 صفحه PDF | دانلود رایگان |

Epstein-Barr virus (EBV) is a human herpes virus that has been associated with several malignancies as Burkitt's lymphoma, nasopharyngeal carcinoma and Hodgkin's disease. All EBV associated malignancies showed a distinct viral gene expression pattern, while Epstein-Barr nuclear antigen 1 (EBNA-1) is constitutively expressed in all such disorders. Here, the development of a biosensor to detect EBNA-1 protein is reported, which was based on a nucleic acid bioreceptor and a quartz crystal microbalance with a dissipation monitoring (QCM-D) transducer. The DNA probe for EBNA-1 detection was designed and synthesized to mimic its palindromic target sites in the EBV genome. This DNA probe was immobilized on the Au-surface of a QCM-D electrode, followed by the blocking of the accessible Au-surface with 6-mercapto-1-hexanol (6-MHO). The system showed a limit of detection of 50 ng/mL in direct detection of EBNA-1, however, the sensitivity was improved by 2 orders of magnitude (0.5 ng/mL) when an amplification cascade, employing antibodies labeled with alkaline phosphatase (AP), was applied to the system.
► The development of a biosensor for label free and amplified detection of EBNA-1 was reported.
► The biosensor was based on a nucleic acid bioreceptor and a QCM-D transducer.
► The system showed a limit of detection of 50 ng/mL in label free detection of EBNA-1.
► The sensitivity was improved by 2 orders of magnitude when an amplification cascade was applied.
Journal: Biosensors and Bioelectronics - Volume 30, Issue 1, 15 December 2011, Pages 272–275