Lecture 7 Web: pollev.com/ucibio Text: To: 37607 Type in: 169964

Lecture 7

Web: pollev.com/ucibio

Text: To: 37607Type in: 169964 <your

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The importance of structure

“Chaperones” & protein foldingMisfolded proteins are very, very bad!E.g. Huntington’s disease

E.g. Prions

Aggregation of mutant Huntington’s

“Tag” protein - GFP

Put “tagged” proteins in cellsCompare: - Normal - Mutant

Prions are WHACK proteins!

Normal vs Disease = Same gene (no mutations!)Put Prion version into normal cells

Prion Normal = Diseased!

Prion protein changes 3D conformation

Working with proteins

Interested in studying Hexokinase

How many proteins in cell?

First step in studying Hexokinase?

How do you know when you have purified Hexokinase?

Estimating purity

First step – how do we know our protein is present?

How do we know how pure our protein is?

Estimating purity

Assume 100 proteins in cell. 1g of each protein.Total protein? Ratio of our protein?Purify: Get rid of 50 unwanted proteins.Total protein? Ratio of our protein?Purify: Get rid of 40 remaining unwanted proteins.Total protein? Ratio of our protein?Purify: Get rid of 8 remaining unwanted proteins.Total protein? Ratio of our protein?Ratio of activity of protein:Total protein = Specific activity

Specific activity table

Purifying proteins

1st step = Getting protein!

- Lyse

- “Fractionate”

Cell fractionation by centrifugation

Purifying proteins

What properties of proteins can you exploit?

Changing protein solubility – Salting in/out

http://www.foodnetworksolution.com/wiki/word/1820/salting-out

Changing protein solubility: pH & Charge

http://elte.prompt.hu/sites/default/files/tananyagok/practical_biochemistry/ch05s04.html

Column chromatography: General principle

Gel filtration column: Size

Ion exchange column: Charge

Affinity column

Immunoprecipitation

Immunoprecipitation