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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 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 pentapeptide has the sequenceNNKNN(using one-letter symbols for amino acids). Calculate the mass of this peptide, as determined by mass spectrometry, to three significant figures.

Separate cleavage reactions of a polypeptide by CNBr and chymotrypsin yield fragments with the following amino acid sequences. What is the sequence of the intact polypeptide?

CNBr treatment

1. Argโ€“Alaโ€“Tyrโ€“Glyโ€“Asn

2. Leuโ€“Pheโ€“Met

3. Aspโ€“Met

Chymotrypsin

4. Metโ€“Argโ€“Alaโ€“Tyr

5. Aspโ€“Metโ€“Leuโ€“Phe

6. Glyโ€“Asn

Explain why a certain protein has an apparent molecular mass of 90kDwhen determined by gel filtration and 60kDwhen determined by SDS-PAGE in the presence or absence of 2-mercaptoethanol. Which molecular mass determination is more accurate?

You are using ammonium sulphate to purify protein Q (pI = 5.0) by salting out from a solution at pH 7.0. How should you adjust the pH of the mixture to maximize the amount of protein Q that precipitates?

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