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Mystery of the Crooked Cell:

Mystery of the Crooked Cell:. Investigate Sickle Cell Anemia Using Gel Electrophoresis. Module developed at Boston University School of Medicine. Presented by Dr. Dan Murray. Outline. Sickle Cell Anemia Central Dogma of Biology Genetic Code Hemoglobin Electrophoresis. Sickle Cell Anemia.

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Mystery of the Crooked Cell:

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  1. Mystery of the Crooked Cell: Investigate Sickle Cell Anemia Using Gel Electrophoresis Module developed at Boston University School of Medicine Presented by Dr. Dan Murray

  2. Outline • Sickle Cell Anemia • Central Dogma of Biology • Genetic Code • Hemoglobin • Electrophoresis

  3. Sickle Cell Anemia

  4. Sickle Cell Anemia • Genetic Disease • Heterozygous individuals – carriers • Homozygous individuals – diseased • Hemoglobin • Found in red blood cells • Carries oxygen to tissues • SCA Results from Defective Hemoglobin • Hemoglobins stick together • Red blood cells damaged • Complications from low oxygen supply to tissues • Pain, organ damage, strokes, increased infections, etc. • Incidence highest among Africans and Indians • Heterozygotes protected from Malaria

  5. Central Dogma of Biology

  6. Central Dogma of Biology Transcription: Conversion of information from DNA to mRNA Translation: Conversion of information from RNA to protein

  7. The Genetic Code

  8. The Genetic Code start

  9. The Genetic Code • Protein chains always begin with Met • 53 orientation corresponds to • N-term  C-term orientation mRNA sequence 5’ 3’ AUG AAC AAU GCG CCG GAG GAA GCG GAG Met---Asn---Asn---Ala Met---Asn---Asn---Ala---Pro---Glu---Glu---Ala---Glu Met---Asn Met---Asn---Asn Met N-terminus C-terminus Protein sequence

  10. Hemoglobin

  11. Hemoglobin • Multi-subunit protein (tetramer) • 2  and 2  subunits • Heme • One per subunit • Has an iron atom • Carries O2 • In red blood cells

  12. Sickle Cell Hemoglobin Normal mRNA GUG CAC CUG ACU CCU GAG GAG AAG val his leu thr pro glu glu lys 1 2 3 4 5 6 7 8 Normal protein Mutation (in DNA) Mutant mRNA GUG CAC CUG ACU CCU GUG GAG AAG val his leu thr pro val glu lys 1 2 3 4 5 6 7 8 Mutant protein Glutamate (glu), a negatively charged amino acid, is replaced by valine (val), which has no charge.

  13. Sickle Cell Hemoglobin Significant change in structure caused by the single mutation http://webpub.alleg.edu/dept/bio/bio221/Discussion/hbBoth.gif

  14. A Possible Cure for Sickle Cell Anemia? • During fetal development, a different gene (gamma) produces hemoglobin • Expression of gamma gene stops naturally during development • Research efforts focused on stopping silencing of gamma gene • Would provide sickle cell patients with good hemoglobin

  15. Electrophoresis

  16. Gel Electrophoresis Method for separating molecules (DNA, proteins, etc.) on the basis of physical or chemical properties such as: (1) size (2) shape (3) electrical charge

  17. Electrophoresis of DNA • Gels are made of agarose or polyacrylamide • DNA samples loaded, voltage applied • Negatively charged DNA migrates toward “+” electrode • Smaller DNA fragments migrate faster

  18. Electrophoresis of Proteins • More complex than DNA electrophoresis • Different proteins have different charges • Proteins vary widely in shape • Polyacrylamide is usually the gel medium

  19. Protein ElectrophoresisNon-Denaturing conditions • Non-denaturing (native): no pretreatment of proteins before electrophoresis • Proteins retain normal shape • Proteins retain normal charge • Proteins separated on basis of charge, size, and shape +2 30kD 4 42kD

  20. Non-Denaturing Electrophoresis of Normal and Mutant Hemoglobin Charge, Size, Shape Q. Which of the above properties will be different for normal Hemoglobin (HgA) and mutant Hemoglobin (HgS)? A. Charge: Yes, HgA has one “–” more than HgS. Size: No, HgA and HgS are the same size. Shape: Yes, the shapes are different.

  21. Migration Rates of Normal and Mutant Hemoglobin Which Hg migrates faster during electrophoresis? HgA has one more “” than HgS  Amino acids Val and Glu about same size NA NA HgA more compact than HgS 

  22. Protein Structure

  23. Protein Structure • 1 = Primary Structure • 2 = Secondary Structure • 3 = Tertiary Structure • 4 = Quaternary Structure

  24. Primary Structure Definition - Sequence of amino acids in a protein Example – Primary structure of the enzyme lysozyme: 1 2 3 4 5 126 127 128 129 Lys-Val-Phe-Gly-Arg...Gly-Cys-Arg-Leu Note: By convention, amino acid sequences are written starting with the amino terminus.

  25. Secondary Structure Definition – Regular patterns of relatively small segments of a protein held together mainly by H-bonds Examples: -helix -structure http://www.ultranet.com/~jkimball/BiologyPages/S/SecondaryStructure.html

  26. Tertiary Structure Definition – Overall 3-D shape of a protein. Two basic types are globular and fibrous. Examples: Fibrous (Collagen) Globular (Pepsin) http://www.ultranet.com/~jkimball/BiologyPhttp://dwb.unl.edu/Teacher/NSF/C10/C10Links/main.chem.ohiou.edu/~wathen/chem302/protein.htmlages/S/SecondaryStructure.html

  27. Quaternary Structure Definition – Overall 3-D shape of a multi-subunit protein Example: Rabbit muscle glycogen phosphorylase http://bmbiris.bmb.uga.edu/wampler/tutorial/prot4.html

  28. All Levels of Structure http://sosnick.uchicago.edu/precpquastru.html

  29. Protein Electrophoresis Denaturing conditions • Proteins treated with SDS (anionic detergent) before electrophoresis (SDS-PAGE) • SDS molecules bind to the Protein • Proteins lose normal shape • Proteins all have same charge/mass ratio • Proteins are separated on basis of size only ChargeMass +3 30kD 4 42kD ChargeMass 300 30kD 420 42kD SDS treatment

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