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Practical molecular biology

Practical molecular biology. Dr. Alexei Gratchev Prof. Dr. Julia Kzhyshkowska Prof. Dr. W. Kaminski. Course structure. 08.10 Plasmids, restriction enzymes, analytics 09.10 Genomic DNA, RNA 10.10 PCR, real-time (quantitative) PCR 11.10 Protein analysis IHC 12.10 Flow cytometry (FACS).

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Practical molecular biology

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  1. Practical molecular biology Dr. Alexei Gratchev Prof. Dr. Julia Kzhyshkowska Prof. Dr. W. Kaminski

  2. Course structure • 08.10 Plasmids, restriction enzymes, analytics • 09.10 Genomic DNA, RNA • 10.10 PCR, real-time (quantitative) PCR • 11.10 Protein analysis IHC • 12.10 Flow cytometry (FACS)

  3. Nucleic acid chemistry • DNA (deoxyribonucleic acid) and RNA (ribonucleic acid) store and transfer genetic information in living organisms. • • DNA: • – major constituent of the nucleus • – stable representation of an organism’s complete genetic makeup • • RNA: • – found in the nucleus and the cytoplasm • – key to information flow within a cell

  4. Why purifying genomic DNA? • Many applications require purified DNA. • Purity and amount of DNA required (and process used) depends on intended application. • Example applications: • Tissue typing for organ transplant • Detection of pathogens • Human identity testing • Genetic research

  5. DNA purification challenges • Separating DNA from other cellular components such as proteins, lipids, RNA, etc. • Avoiding fragmentation of the long DNA molecules by mechanical shearing or the action of endogenous nucleases.Effectively inactivating endogenous nucleases (DNase enzymes) and preventing them from digesting the genomic DNA is a key early step in the purification process. DNases can usually be inactivated by use of heat or chelating agents.

  6. DNA purification There are many DNA purification methods. All must: • Effectively disrupt cells or tissues(usually using detergent) • Denature proteins and nucleoprotein complexes(a protease/denaturant) • Inactivate endogenous nucleases(chelating agents) • Purify nucleic acid target away from other nucleic acids and protein(could involve RNases, proteases, selective matrix and alcohol precipitations)

  7. Denaturing agents • Ionic detergents, such as SDS, disrupt hydrophobic interactions and hydrogen bonds. • Chaotropic agents such as urea and guanidine disrupt hydrogen bonds. • Reducing agents break disulfide bonds. • Salts associate with charged groups and at low or moderate concentrations increase protein solubility. • Heat disrupts hydrogen bonds and nonpolar interactions. • Some DNA purification methods incorporate proteases such as proteinase K to digest proteins.

  8. DNA isolation DNA must be separated from proteins and cellular debris. Separation Methods • Organic extraction • Salting out • Selective DNA binding to a solid support

  9. Organic extraction • DNA is polar and therefore insoluble in organic solvents. • Traditionally, phenol:chloroform is used to extract DNA. • When phenol is mixed with the cell lysate, two phases form. DNA partitions to the (upper) aqueous phase, denatured proteins partition to the (lower) organic phase. • DNA is a polar molecule because of the negatively charged phosphate backbone. • This polarity makes it more soluble in the polar aqueous phase.

  10. Genomic DNA isolation: phenol extraction 1:1 phenol : chloroform or 25:24:1 phenol : chloroform : isoamyl alcohol • Phenol: denatures proteins, precipitates form at interface between aqueous and organic layer • Chloroform: increases density of organic layer • Isoamyl alcohol: prevents foaming Genomic DNA is isolated as pieces up to 1 Mbp!

  11. Genomic DNA isolation: phenol extraction

  12. Binding to a support material Most modern DNA purification methods are based on purification of DNA from crude cell lysates by selective binding to a support material. Support Materials • Silica • Anion-exchange resin Advantages • Speed and convenience • No organic solvents • Amenable to automation/miniaturization Disadvantage • DNA fragmentation

  13. Silica matrix based genomic DNA isolation

  14. Genomic DNA analysis

  15. Concentration measurement Photometric measurement of DNA concentration UV 260 nm Conc=50xOD260

  16. Total cellular RNA • Messenger RNA (mRNA): 1-5% • Serves as a template for protein synthesis • • Ribosomal RNA (rRNA): >80% • Structural component of ribosomes • • Transfer RNA (tRNA): 10-15% • Translates mRNA information into the appropriate amino acid

  17. What RNA is needed for? Messenger RNA synthesis is a dynamic expression of the genome of an organism. As such, mRNA is central to information flow within a cell. • Size – examine differential splicing • Sequence – predict protein product • Abundance – measure expression levels • Dynamics of expression – temporal, developmental, tissue specificity

  18. RNA isolation

  19. RNA purification • Total RNA from biological samples • – Organic extraction • – Affinity purification • • mRNA from total RNA • – Oligo(dT) resins • • mRNA from biological samples • – Oligo(dT) resins

  20. Total RNA purification • Goal: Isolate RNA from cellular components • – Cells or tissue must be rapidly and efficiently disrupted • – Inactivate RNases • – Denature nucleic acid-protein complexes • – RNA selectively partitioned from DNA and protein • • Isolation from different tissues/sources raises different issues

  21. RNases • RNases are naturally occurring enzymes that degrade RNA • • Common laboratory contaminant (from bacterial and human sources) • • Also released from cellular compartments during isolation of RNA from biological samples • • Can be difficult to inactivate

  22. Protecting agains RNases • Wear gloves at all times • • Use RNase-free tubes and pipet tips • • Use dedicated, RNase-free, chemicals • • Pre-treat materials with extended heat (180°C for several hours), wash with DEPC-treated water, NaOH • or H2O2 • • Supplement reactions with RNase inhibitors • • Include a chaotropic agent (guanidine) in the procedure • – Chaotropic agents such as guanidine inactivate and precipitate RNases and other proteins

  23. Organic extraction of total RNA

  24. Organic extraction of total RNA • Advantages • Versatile - compatible with a variety of sample types • Scalable - can process small and large samples • Established and proven technology • Inexpensive • Disadvantages • Organic solvents • Not high-throughput • RNA may contain contaminating genomic DNA

  25. Affinity purification of total RNA

  26. Affinity purification of total RNA • Advantages • Eliminates need for organic solvents • Compatible with a variety of sample types (tissue, tissue culture cells, white blood cells, plant cells, bacteria, yeast, etc.) • DNase treatment eliminates contaminating genomic DNA • Excellent RNA purity and integrity

  27. RNA analysis Photometric measurement of RNA concentration UV 260 nm Conc=40xOD260

  28. Alternative nucleic acids purification protocol CsCl gradient centrifugation The best quality of RNA RNA and DNA isolated simultaneously has a 36h centrifugation step

  29. Questions?

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