Presentation on theme: "Resolution and Detection of Nucleic Acids"— Presentation transcript:
1Resolution and Detection of Nucleic Acids Chapter 5Resolution and Detection of Nucleic Acids
2ObjectivesExplain the principle and performance of electrophoresis as it applies to nucleic acids.Compare and contrast agarose and polyacrylamide gel polymers.Explain the principle and performance of capillary electrophoresis as it is applies to nucleic acid separation.Describe the general types of equipment used for electrophoresis.Discuss methods and applications of pulsed field gel electrophoresis.Compare and contrast detection systems used in nucleic acid applications.
3Gel ElectrophoresisElectrophoresis is the movement of molecules by an electric current.Nucleic acid moves from a negative to a positive pole.
4Gel ElectrophoresisWhen DNA is applied to a macromolecular cage or gel such as agarose or polyacrylamide, its migration under the pull of the current is impeded.
5The movement of molecules is impeded in the gel so that molecules will collect or form a band according to their speed of migration.% agarose: 2% % %500 bp200 bp50 bp500 bp200 bp50 bp500 bp200 bp50 bpThe concentration of gel/buffer will affect the resolution of fragments of different size ranges.
6Gel ElectrophoresisSlab gel electrophoresis can have either a horizontal or vertical format.Sample is introduced into wells at the top of the gel.
7Very Large DNA Molecules are Separated by Pulsed Field Gel Electrophoresis (PFGE).
8Types of PFGEField inversion gel electrophoresis (FIGE): alternating positive and negative polesTransverse alternative field electrophoresis (TAFE): transverse angle reorientation of poles on a vertical gelContour-clamped homogenous electric field (CHEF): alternating polarity in an electrode arrayRotating gel electrophoresis (RGE): rotating gel with fixed poles
9Polyacrylamide Gel Electrophoresis (PAGE) Acrylamide, in combination with a cross linker, methylene bis-acrylamideSynthetic, consistent polymerPolymerization catalysts: ammonium persulfate (APS) plus N,N,N',N'-tetramethylethylenediamine (TEMED), or light activationResolves 1 bp difference in a 1 kb molecule (0.1% difference)
10Capillary Electrophoresis (CE) Separates solutes by charge/mass ratio.Capillary gel electrophoresis is used to separate nucleic acids.=+ ++++-
11Capillary Gel Electrophoresis (CGE) Thin glass (fused silica) capillary 30 to 100 cm X 25–100 mm internal diameterLinear or cross-linked polyacrylamide or other linear polymers used for sievingSeparation based on sizeMore rapid, automated than slab gelsRun at higher charge per unit areaElectrokinetic injection of sample
12Electrophoresis Buffers Carry current and protect samples during electrophoresis.Tris Borate EDTA (TBE), Tris Acetate EDTA (TAE), Tris Phosphate EDTA (TPE) used most often for DNA.10 mM sodium phosphate or MOPS buffer used for RNA.Buffer additives modify sample molecules.Formamide, urea (denaturing agents)
13Electrophoresis Equipment Horizontal or submarine gel
15Electrophoresis Equipment Combs are used to put wells in the cast gel for sample loading.Regular comb: wells separated by an “ear” of gelHoundstooth comb: wells immediately adjacent
16Running a Gel Use the proper gel concentration for sample size range. 0.5–5% agarose3.5–20% polyacrylamideUse the proper comb (well) and gel size.
17Running a GelLoad sample mixed with tracking dye (dye + density agent).
18Running a Gel Detect bands by staining during or after electrophoresis Ethidium bromide: for double-stranded DNASyBr green or SyBr gold: for single- or double-stranded DNA or for RNASilver stain: more sensitive for single- or double-stranded DNA or for RNA and proteins
19SummaryElectrophoresis is used to separate molecules by size and/or charge.Nucleic acid fragments can be resolved on agarose of polyacrylamide gels.PFGE is used to resolve very large DNA fragments.CGE is more rapid and automated than slab gel electrophoresis.The choice of electrophoresis method depends on the type and size of sample.