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Protein Purification

Protein Purification. Fig. 5-CO, p.113. Protin Purificartion & Characterizing Techniques. 1. How Do We Extract Pure Proteins from Cells?

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Protein Purification

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  1. Protein Purification Fig. 5-CO, p.113

  2. Protin Purificartion & Characterizing Techniques 1. How DoWe Extract Pure Proteins from Cells? Disruption of cells is the first stepinproteinpurification.Thevariouspartsofcellscanbeseparatedbycentrifugation.Thisisausefulstepbecauseproteinstendtooccuringivenorganelles.Highsaltconcentrationswillprecipitategroupsofproteins,whicharethenfurtherseparatedbychromatographyandelectrophoresis.

  3. 2.WhatIsColumnChromatography? Twoofthemostimportantmethodsforseparatingaminoacids,peptides,andproteinsarechromatographyandelectrophoresis.Thevariousformsofchromatographyrelyondifferencesincharge,polarity,orsizeofthemoleculestobeseparated,dependingontheapplication.

  4. 3. What Is Electrophoresis? In electrophoresis, differences in charge and in size are the criteria for separation. Thesievingactionofgelslabsisusedinconjunctionwiththechargeonproteinstoachieveseparation.Theelectrophoreticmobilitiesofproteinscanbeusedtoestimatetheirmolecularweights.

  5. 4.HowDoWeDeterminethePrimaryStructureofaProtein? DeterminationoftheN-terminalandC-terminalaminoacidsofproteinsdependsontheuseoftheseseparationmethodsaftertheendsofthemoleculehavebeenchemicallylabeled.Selectivecleavageoftheproteinintopeptidesbyenzymaticorchemicalhydrolysisproducesfragmentsofmanageablesizeforsequencing.

  6. PROTEINS & PEPTIDES MUST BE PURIFIED PRIOR TO ANALYSIS Highly purified protein is essential for determination of its amino acid sequence. Cells contain thousands of different proteins, each in widely varying amounts. The isolation of a specific protein in quantities sufficient for analysis presents a challenge that may require multiple successive purification techniques.

  7. Table 5-1, p.114

  8. Dialysis. Protein molecules (red) are retained within the dialysis bag, whereas small molecules (blue) diffuse

  9. Fig. 5-1, p.115

  10. Gel-Filtration Chromatography Fig. 5-2, p.116

  11. 33 Fig. 5-3, p.117

  12. Fig. 5-5a, p.118

  13. Fig. 5-5b, p.118

  14. Affinity Chromatography Fig. 5-6, p.118

  15. Affinity Chromatography Affinity chromatography of concanavalin A (shown in yellow) on a solidsupport containing covalently attached glucose residues (G). The plant protein concanavalin A can be purified by passing a crude extract through a column of beads containing covalently attached glucose residues. Concanavalin A binds to such a column because it has affinity for glucose, whereas most other proteins do not. The bound concanavalin A can then be released from the column by adding a concentrated solution of glucose.

  16. Ion-Exchange Chromatography.This technique separates proteins mainly according to their net charge.

  17. Ion-Exchange Chromatography. Fig. 5-8, p.120

  18. Fig. 5-7a, p.119

  19. Fig. 5-7b, p.119

  20. Fig. 5-9, p.120

  21. Chromatographic Separations Partition molecules between two phases, one mobile and the other stationary. For separation of amino acids or sugars, the stationary phase, or matrix, may be a sheet of filter paper (paper chromatography) or a thin layer of cellulose, silica, or alumina (thin-layer chromatography);

  22. Electrophoresis • Electrophoresis: the process of separating compounds on the basis of their electric charge & size • electrophoresis of amino acids can be carried out using paper, starch, agar, certain plastics, and cellulose acetate as solid supports • in paper electrophoresis, a paper strip saturated with an aqueous buffer of predetermined pH serves as a bridge between two electrode vessels.

  23. a sample of amino acids is applied as a spot (the origin) on the solid support strip • an electric potential is applied to the electrode vessels and amino acids migrate toward the electrode with charge opposite their own • molecules with a high charge density move faster than those with a low charge density • molecules at their isoelectric point remain at the origin • after separation is complete, the strip is dried and developed to make the separated amino acids visible

  24. Fig. 5-10, p.121

  25. Polyacrylamide Gel Electrophoresis.

  26. Fig. 5-11, p.121

  27. Electrophoretic Analysis of a Protein Purification.

  28. Fig. 5-12, p.121

  29. Two-Dimensional Gel Electrophoresis. Fig. 5-13, p.122

  30. molecular weights of sample proteins

  31. How Do We Determine the Primary Structure of a Protein? How Do We Determine the Primary Structure of a Protein?

  32. Fig. 5-14, p.123

  33. Fig. 5-16, p.124

  34. Fig. 5-17, p.125

  35. Chemical CleavageCyanogen bromide Fig. 5-18b, p.125

  36. Edman reagent is phenylisothiocyanate

  37. Specific cleavage of polypeptides

  38. Fig. 5-15, p.123

  39. Fig. 5-18a, p.125

  40. Fig. 5-19, p.126

  41. END

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