Biomedical Engineering Reference
In-Depth Information
Fig. 3.4
A schematic representation of His
6
-peptide-linker-facilitated self-assembly of a molec-
ular beacon structure with or without the complementary DNA. Reprinted with the permission
from Ref. [
12
]. Copyright 2007 American Chemical Society (
a
) and the QD-MB-AuNP probe
with or without presence of the complementary viral RNA (
b
). Reproduced with permission from
Ref. [
13
]. Copyright 2010, Royal Society of Chemistry
between internal hybridization within the stem structure and hybridization between
the target and the loop structure [
15
]. Owing to such high specificity, MB has been
commercially used in PCR or reverse transcriptase PCR (RT-PCR) kit. As illustrated
above, fluorophore and quencher are tagged to each end of the MB. When the bea-
con unfolds in the presence of the complementary target sequence, the fluorescence of
fluorophore will be recovered. The amount of fluorescence at any given cycle, or fol-
lowing cycling, depends on the amount of specific product and can be easily detected