Nucleic Acids Research, 2002, Vol. 30, No. 19 4208-4215
© 2002 Oxford University Press
Structure–function relationships of shared-stem and conventional molecular beacons
Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, 315 Ferst Drive, Suite 2306, Atlanta, GA 30332, USA and 1 Integrated DNA Technologies, Inc., Coralville, IA 52241, USA
*To whom correspondence should be addressed. Tel: +1 404 385 0373; Fax: +1 404 894 4243; Email: gang.bao{at}bme.gatech.edu
Molecular beacons are oligonucleotide probes capable of forming a stem–loop hairpin structure with a reporter dye at one end and a quencher at the other end. Conventional molecular beacons are designed with a target-binding domain flanked by two complementary short arm sequences that are independent of the target sequence. Here we report the design of shared-stem molecular beacons with one arm participating in both stem formation when the beacon is closed and target hybridization when it is open. We performed a systematic study to compare the behavior of conventional and shared-stem molecular beacons by conducting thermodynamic and kinetic analyses. Shared-stem molecular beacons form more stable duplexes with target molecules than conventional molecular beacons; however, conventional molecular beacons may discriminate between targets with a higher specificity. For both conventional and shared-stem molecular beacons, increasing stem length enhanced the ability to differentiate between wild-type and mutant targets over a wider range of temperatures. Interestingly, probe–target hybridization kinetics were similar for both classes of molecular beacons and were influenced primarily by the length and sequence of the stem. These findings should enable better design of molecular beacons for various applications.
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