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Explain how you would use salting out to prepare a more concentrated solution of a protein.

Short Answer

Expert verified

Many undesirable proteins are removed from a solution containing a variety of proteins by lowering the salt concentration to just below the precipitation point of the protein to be purified. The salt concentration of the resulting solution is then raised to precipitate the target protein after the precipitated proteins have been removed by filtration or centrifugation. This process will purify and will give a concentrated solution of desired protein.

Step by step solution

01

Factors that affect proteins solubility

A protein has numerous charged groups and because of that its solubility is affected by dissolved salt concentrations, solvent polarity, pH, and temperature. Some of these variables can be changed to cause specific proteins to precipitate while other proteins remain soluble.

02

Salting out

Salting out is a purification procedure that takes advantage of particular compounds' reduced solubility in a solution with a very high ionic strength.The salting out effect occurs due to competition for solvent molecules between the added salt ions and the other dissolved solutes.

Fig: Fractionation by salting out. (a) Salt is added to solution of mixed protein molecules at a concentration which is slightly below the salting-out point of the target protein (Blue). (b) Unwanted proteins (Red) are precipitated which are discarded. More salt is added in the supernatant to bring the concentration which is sufficient to precipitate the target protein. (c) After centrifugation the target protein is recovered as precipitate and added in suitable buffer.

03

Explanation

Salting out is the basis of one of the most widely used protein purification techniques because various proteins have distinct ionic and hydrophobic compositions and so they precipitate at varying salt concentrations.

So, if we increase the salt concentration of the solution to a point which is higher than the salting-out point for the desired protein, we can obtain a concentrated solution of a desired protein.

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Most popular questions from this chapter

You are trying to purify a protein that is soluble in a solution of 2 M ammonium sulfate. After centrifugation to remove other proteins that have precipitated at this high salt concentration, you recover the supernatant to assay the target proteinโ€™s activity in a cell culture system.

(a) Explain why the cells die when incubated with the supernatant.

(b) What procedure could you perform to correct the problem? (Hint: See Section 2-1D).

You wish to determine the sequence of a polypeptide that has the following amino acid composition.

1 Ala 4 Arg 2 Asn 3 Asp 4 Cys 3 Gly 1 Gln 4 Glu 1 His 1 Lys 1 Met 1 Phe 2 Pro 4 Ser 2 Tyr 1 Trp

(a) What is the maximum number of peptides you can expect if you cleave the polypeptide with cyanogen bromide?

(b) What is the maximum number of peptides you can expect if you cleave the polypeptide with chymotrypsin?

(c) Analysis of the intact polypeptide reveals that there are no free sulfhydryl groups. How many disulfide bonds are likely to be present?

(d) How many different arrangements of disulfide bonds are possible?

(a) The ESI-MS spectrum below was obtained for hen egg-white lysozyme (HEWL). Using peaks 5 and 6, calculate the molecular mass of HEWL (see Sample Calculation 5-1).

[http://www.astbury.leeds.ac.uk/facil/MStut/mstutorial.htm. Published by A.E. Ashcroft, Astbury Centre for Structural Molecular Biology, University of Leeds (2000)]

(b) What is the charge on the ion that makes peak 5?

Protein X has an absorptivity of 0.4mL ยท mg-1ยท cm-1 at 280nm. What is the absorbance at 280nm of a 2.0 mg ยท mL-1solution of protein X? (Assume the light path is 1cm.)

You must cleave the following peptide into smaller fragments. Which of the proteases listed in Table 5-4 would be likely to yield the most fragments? The fewest?

NMTQGRCKPVNTFVHEPLVDVQNVCFKE

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