Molecular beacon

From Wikipedia, the free encyclopedia
Structure of molecular beacons in their native conformations (top) or hybridized with a DNA strand (bottom)

Molecular beacons, or molecular beacon probes, are oligonucleotide hybridization probes that can report the presence of specific nucleic acids in homogenous solutions. Molecular beacons are hairpin-shaped molecules with an internally quenched fluorophore whose fluorescence is restored when they bind to a target nucleic acid sequence. This is a novel non-radioactive method for detecting specific sequences of nucleic acids. They are useful in situations where it is either not possible or desirable to isolate the probe-target hybrids from an excess of the hybridization probes.

Molecular beacon probes[]

The structure of a typical molecular beacon probe

A typical molecular beacon probe is 25 nucleotides long.[citation needed] The middle 15 nucleotides are complementary to the target DNA or RNA and do not base pair with one another, while the five nucleotides at each terminus are complementary to each other rather than to the target DNA. A typical molecular beacon structure can be divided in 4 parts: 1) loop, an 18–30 base pair region of the molecular beacon that is complementary to the target sequence; 2) stem formed by the attachment to both termini of the loop of two short (5 to 7 nucleotide residues) oligonucleotides that are complementary to each other; 3) 5' fluorophore at the 5' end of the molecular beacon, a fluorescent dye is covalently attached; 4) 3' quencher (non fluorescent) dye that is covalently attached to the 3' end of the molecular beacon. When the beacon is in closed loop shape, the quencher resides in proximity to the fluorophore, which results in quenching the fluorescent emission of the latter.

If the nucleic acid to be detected is complementary to the strand in the loop, the event of hybridization occurs. The duplex formed between the nucleic acid and the loop is more stable than that of the stem because the former duplex involves more base pairs. This causes the separation of the stem and hence of the fluorophore and the quencher. Once the fluorophore is no longer next to the quencher, illumination of the hybrid with light results in the fluorescent emission. The presence of the emission reports that the event of hybridization has occurred and hence the target nucleic acid sequence is present in the test sample.

Use in Cell Engineering (Chromovert Technology)[]

In a cell engineering process named Chromovert Technology, fluorogenic signaling oligonucleotide probes were reported for use to detect and isolate cells expressing one or more desired genes, including the production of multigene stable cell lines expressing heteromultimeric epithelial sodium channel (αβγ-ENaC), sodium voltage-gated ion channel 1.7 (NaV1.7-αβ1β2), four unique γ-aminobutyric acid A (GABAA) receptor ion channel subunit combinations α1β3γ2s, α2β3γ2s, α3β3γ2s and α5β3γ2s, cystic fibrosis conductance regulator (CFTR), CFTR-Δ508 and two G-protein coupled receptors (GPCRs).[1] Research Foundation to Cure AIDS is also using Chromovert Technology to increase the efficiency of cell engineering strategies to cure HIV-infection.

Synthesis[]

Main article: Oligonucleotide synthesis

Molecular beacons are synthetic oligonucleotides whose preparation is well documented. In addition to the conventional set of nucleoside phosphoramidites, the synthesis also requires a solid support derivatized with a quencher and a phosphoramidite building block designed for the attachment of a protected fluorescent dye.

The first use of the term molecular beacons, synthesis and demonstration of function was in 1996.[2]

Alternative homogeneous assay technologies[]

  • 5'-nuclease TaqMan assay[3]
  • Exciton-controlled hybridization-sensitive fluorescent oligonucleotide (ECHO) probes.[4]
  • Dual Hybridization (LightCycler®) probes
  • Scorpions® Probes
  • LUX (Light Upon Extension) Probes
  • DNA binding dye assays (e.g., SYBR Green, SYTO9, Melt Doctor, LCGreen Plus, etc.)

Applications[]

  • SNP detection[3]
  • Real-time nucleic acid detection
  • Real-time PCR quantification
  • Allelic discrimination and identification[3]
  • Multiplex PCR assays
  • Diagnostic clinical assays

References[]

  1. ^ Shekdar K, Langer J, Venkatachalan S, Schmid L, Anobile J, Shah P, et al. (March 2021). "Cell engineering method using fluorogenic oligonucleotide signaling probes and flow cytometry". Biotechnology Letters. doi:10.1007/s10529-021-03101-5. PMC 7937778. PMID 33683511.
  2. ^ Tyagi S, Kramer FR (March 1996). "Molecular beacons: probes that fluoresce upon hybridization". Nature Biotechnology. 14 (3): 303–8. doi:10.1038/nbt0396-303. PMID 9630890. S2CID 27010207.
  3. ^ Jump up to: a b c Täpp I, Malmberg L, Rennel E, Wik M, Syvänen AC (April 2000). "Homogeneous scoring of single-nucleotide polymorphisms: comparison of the 5'-nuclease TaqMan assay and Molecular Beacon probes". BioTechniques. 28 (4): 732–8. doi:10.2144/00284rr02. PMID 10769752.
  4. ^ Okamoto A (December 2011). "ECHO probes: a concept of fluorescence control for practical nucleic acid sensing". Chemical Society Reviews. 40 (12): 5815–28. doi:10.1039/c1cs15025a. PMID 21660343.
Retrieved from ""