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Nucleic acid-based methods (I). Structure of DNA . Complementality of DNA (high specificity in base paring). Replication of DNA . Easy manipulation of DNA . Hybridization. Nucleic acid-based methods . Gene probing Colony hybridization Southern/Northern hybridization Microarray
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Nucleic acid-based methods • Gene probing • Colony hybridization • Southern/Northern hybridization • Microarray • Polymerase Chain Reaction (PCR) • PCR • RT-PCR • Multiplex PCR • Nested PCR
Gene probes • Small pieces of DNA complementary to the target sequence of interest • Labeling options • Radioactive chemicals • Nonradioactive alternatives (DIG, biotin, or fluorescein)
Microbe Nucleic Acid Detection by DNA Microarrays or “Gene Chip” Technology Generate/obtain DNA complimentary to genes (sequences) of interest; • 1000s of different ones Apply tiny quantities of each different one onto solid surfaces at defined positions • “gene chip” or “DNA microarray” Isolate or amplify target NA of interest and label with a fluorescent probe Apply sample NA to the “gene chip” surface • Sample NA binds to specific DNA probes on chip surface; wash away unbound NA Detect bound DNA or RNA by fluorescence after laser excitation Analyze hybridization data using imaging systems and computer software Fluorescing Gene Chip or DNA Microarray
Primers and enzymes • Primers • Short nucleotides complementary to a target DNA • Upstream and downstream primers • Taq polymerase • Heat stable DNA-dependant DNA polymerase • Isolated from thermophilic bacteria (Thermus aquaticus) • Withstand temperature up to 98oC
Different PCR techniques • PCR • RT-PCR • Multiplex PCR • Nested PCR
Agarose Gel Electrophoresis • Separate nucleic acid fragments in an agarose gel • Resolves small DNA molecules: 0.1 to 50 kb • % agarose determines resolution of DNA size: • 0.3% w/v: resolves 5 to 50 kb • 2% w/v resolves 0.1 to 2 kb • Resolving large molecules (up to 500 kb) requires specialized methods • Pulse-field gel electrophoresis (PFGE) DNA marker ladder Specific DNA fragment
Example: RT-PCR and Oligoprobe Detection of Enteroviruses in Water
Real-Time PCR and Quantitative Fluorogenic Detection • Molecular beacon. Several 5' bases form base pairs with several 3' bases; reporter and quencher in close proximity. • If reporter is excited by light, its emission is absorbed by quencher & no fluorescence is detected. • Detection of PCR product by molecular beacon. • Beacon binds to PCR product and fluoresces when excited by the appropriate of light. • [Fluorescence] proportional to [PCR product amplified]