Molecular Diagnostic II: Protein Techniques Flashcards

1
Q

Improving on insulin

A

Lispro (Eli Lilly): insulin analogue. Faster acting, more readily absorbed than normal insulin, tighter glycemic control

Insulin aspart (NovoLog): behaves similarly to lispro

Insulin glargine (Sanofi-Aventis): longer acting analogue of insulin

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2
Q

Antibody structure

A

Monoclonal antibodies (mAbs) can come from a hybridoma

Hybridoma: B cell (very specific) + myeloma (cancerous plasma cell that is immortal)

Specific for a single epitope generated by single clones of immortalized B lymphocytes

Heavy and light chains, antigen binding site (near Fab domain). The Fc domain is the support part

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3
Q

Processing of insulin

A

Preproinsulin (signal peptide, C chain, A/B chain)

Proinsulin (C chain, A/B chain)

Insulin (A/B chain

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4
Q

Epitope

A

is the specific site on the antigenic molecule

recognized by the Fab region (group of amino acids is recognized on antigen)

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5
Q

B cells can make antibodies

A

True

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6
Q

Polyclonal antibody vs monoclonal antibody

A

Monoclonal=specific for 1 thing

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7
Q

Monoclonal antibody

A

short-lived antibody producing cell

B cell(antibody) + myeloma cell (immortal)

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8
Q

ELISA: HIV

A

Looking for antibody

(Indirect: antigen coated well)

Can give false positives, so we use western to double check)

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9
Q

Sandwich ELISA

A

Antibody coated well

Allowing both the detection and the quantitation of antigen

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10
Q

ELISA: troponin

A

Looking for troponin T,I,C

Plate coated with antibodies (looking for antigen of Troponin T)

Troponin T and I ↑ in serum after myocardial infarction (escape b/c of damage)

Markers of acute ischemia along with myoglobin and creatine kinase

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11
Q

ELISA: Hormones

A

Sandwich method used

Pregnancy test-free monoclonal anitbody for hCG is used

Sandwich formed by combination of capture antibody and free antibody when hCG is present, creating a color change

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12
Q

Western blotting

A

Compare protein levels
Proteins separated by size

Steps:

  1. Protein mix is separated by SDS (gives negative charge)
  2. Transferred to nitrocellulose (b/c proteins are trapped in gel)
  3. Blocked to reduce non-specific interactions
  4. Add 1st antibody (against target protein)
  5. Add 2nd antibody (against 1st antibody)

Detection using:

  • HRP (horseradish peroxidase): turns brown
  • Alkaline phosphatase (AP): dark blue/purple
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13
Q

Proteomics

A

Study of structure/function of proteins

Analysis of protein expression and/or alteration

Post-translational Modifications

“Fishing expedition”-just looking at lots of stuff

knockout vs wild type

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14
Q

2D gel electrophoresis

A

pH + size–> Use 3 colors: “young, old, standard”–>overlay images–>cut out spots–>mass spec–>break proteins into small fragments and bombard w/ electrons to ionize them–> cluster analysis

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