BIC Lecture 6

Card Set Information

Author:
DesLee26
ID:
283068
Filename:
BIC Lecture 6
Updated:
2014-09-14 20:56:37
Tags:
Sam
Folders:
BIC
Description:
Test One
Show Answers:

Home > Flashcards > Print Preview

The flashcards below were created by user DesLee26 on FreezingBlue Flashcards. What would you like to do?


  1. Characterization: 

    What do you want to know about your protein?
    SDS-PAGE: size

    Polarity: Isoelectric focusing, amino acid sequence--> amount/ different and expensive

    • Function in a physiological functional environment: where is it used and can we deduce its function
    • Evolutionarily, is it a member of a fam? 

    Shape of protein: interaction/ if enzyme, active site--> make drug to interact with the active sites
  2. Techniques

    1) amino acid analysis
    protein isolated and purified--> want a list of amino acids and relative proteins--> Amino acid analysis

    Easier than getting a seequence
  3. What are the steps to amino acid analysis
    1) put protein in glass bottle with 6 M HCl and hook tube to vacuum pump--> stick in heating block at close to 100 degrees Celsium

    Required to chop up every peptide bond in the protein
  4. In our mixture, what do we have? What do we do with it?
    we have individual amino acids

    We take our mix and pass through HPLC because it separates molecules that are very similar in size, structure, and characteristics
  5. At end of HPLC is what? 

    Allows what? What is the problem with this? How is it resolved?
    at end is a spectrophotometer, whcih allows us to see what comes out. 

    Problem: how many amino acids can we see with spec? Only two--> tryptophan and tyrosine

    We covalently link ninhydrin to amino acids so we can see them

    We then set the spec at a particular wavelength.
  6. After setting the spec, what?
    we pass amino acids through the HPLC column; amino acids are separated on teh basis of charge, etc. 

    They come out in a very specific order at a specific time.
  7. What is the result of AAA?

    Why is it useful?
    Result: a series of peaks, the size is proportional to the amount present

    It is useful because some proteins have unique compositions (ex: collagen)
  8. Summarize AAA?
    mixture --> HPLC--> spec--> graph
  9. Edman degradation does what?

    Components?
    breaks bonds one at a time

    • - HPLC Colum
    • - spectrophotometer
    • - Chamber with little disk that protein goes into, causing the disk to bind at the C-terminus end of polypeptide with N-terminus floating up
  10. What happens in Edman degradation?
    in stepwise fashion, the amino acid at the terminal amino end is removed

    o Phenyl isothiocyanate reacts with the uncharged terminal amino group of the peptide to form a phenylthiocaramoyl derivative. Then, under mildly acidic conditions, a cyclic derivative of the terminal amino acid is liberated, which leaves an intact peptide shortened by one amino acid
  11. What do you when a bond is broken?
    wash the amino acid, figure out which it is with the spectrophotometer, repeat
  12. Summary of Edman Degradation
    adjust conditions--> label--> cleave first amino acid--> wash through HPLC--> identify by spec reading--> one peak--> repeat

    Time determines what it is
  13. What happens as the rounds of ED increase?
    the residual peaks may show up in the reading if you missed some. Eventually, there are so many peaks, you cannot distinguish the cleaved one from teh previous
  14. As a result of this limitation of ED, what is ED restricted to?
    only proteins with a certain number of amino acids
  15. What is the solution for ED?
    cut the protein into smaller fragments, separate them by HPLC

    Then you need to know which fragment comes before the other. So, you cut the protein with a chemical or enzymatic reagent (use specific cleavage of proteins). And, do the amino acid sequence oer with the new polypeptides. Once this is done, you get the overlaps that are preesent and determine the sequence from there
  16. What is the overall problem with ED?
    expensive and time consuming and requires a lot of protein
  17. Cheaper way of doing things?
    clone genes and translate into amino acids or reverse transcription to determine the codons
  18. How do you answer the question of where the protein is used?
    use antibodies.
  19. How to generate antibodies against a protein?
    injuect into host--> recognized as foreign--> antibodies form
  20. Structure of antibodies
    four chains held by disulfide linages. Two heavy and two light chains
  21. What makes antibodies unique?
    the two ends make it unique. It is the antigen-binding site created with amino acids that will bind to invaders with high degrees of affinity to epitopes on teh antigen
  22. Explain the features of the antigen
    Different structural features on the surface of the molecule that the antibody binds to = epitope

    Forms different antibody for each epitope
  23. Polyclonal antibodies
    makes multiple clones of each antibody that recognizes different epitopes on the same antigen
  24. Monoclonal antibodies
    grabs teh antibody that binds to just the epitope that we need that is in teh antigen

What would you like to do?

Home > Flashcards > Print Preview