PCR Basics.ppt

PCR Basics Purpose of PCR Overview Components of PCR Reaction Variables Temperature Cycle Times and Numbers Primer Buffer Polymerase Experimental Notes Polymerase Chain Reaction “Amplify” large quantities of DNA (μg quantities) from small quantities (ag quantities) [Trillion fold amplification] Analyze single DNA fragments out of large complex mixture. [ Human genome mixture of 12 million 300bp fragments] Alter DNA sequence – directed mutagenesis. Overview of PCR PCR Amplification Exponential Amplification Components of PCR Reaction Template DNA Flanking Primers Thermo-stable polymerase Taq Polymerase dNTP (dATP, dTTP, dCTP, dGTP) PCR Buffer (mg++) Thermocyler PCR Variables Temperature Cycle Times and Temps Primer Buffer Polymerase Temperature Denaturation Trade off between denaturing DNA and not denaturing Taq Polymerase Taq half-life 40min at 95 °, 10min at 97.5° 95° Annealing Trade off between efficient annealling and specificity 2-5 ° below Tm Extension Temperature optimum for Taq Polymerase 72 ° Cycle Times and Temps Typical PCR Run Step Time/Temp 3 min at 95° 30 sec at 95° 1 min at 55° 2 min at 72° Go to step 2 - 29 times 8 min 72° 0 min 4° End Primers Paired flanking primers Length (17-28bp) GC content 50-60% GC Clamp Tm’s between 55-80 Avoid simple sequences – e.g. strings of G’s Avoid primer self complementary e.g. hairpins, homodimers, heterodimers PCR Buffer Basic Components 20mM Tris-HCL pH 8.4 50mM KCl 1.5 mM MgCl2 Magnesium – Since Mg ions form complexes with dNTPs, primers and DNA templates, the optimal concentration of MgCl2 has to be selected for each experiment. Too few Mg2+ ions result in a low yield of PCR product, and too many increase the yield of non-specific products and promote misincorporation. Potential Additives Helix Destabilisers - useful when target DNA is high G/CWith NAs of high (G+C) content. dimethyl sulphoxide (DMSO), dimethyl formamide (DMF), urea formamide? Long Targets 1kb. Formamide and glycer