Question

Calculate the expected A280 of a 1.50 mg/ml solution of bovine serum albumin, based on the amino acid composition (Table 1-1,


calculate the expected absorbace at 280 nm of a 1.5 mg/ml solution of bovine serum albumin based on the amino acid composition. all cysteins are involved in disulfide bonds.
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Answer #1

From Beer Lambert law, Absorbance = \varepsilon cl where \varepsilon is the molar extinction coefficient in M​​​​​​-1​​​​​​​cm -1, c is the concentration of the protein in M and l is the path length (usually taken as 1 cm).

Concentration of the given BSA = 1.5 mg/ml = 1.5 gram/litre = (1.5/66153) mole/litre = (2.27 x 10-5) M

[Molecular weight of BSA given = 66153 Da. Mass/Molecular weight = Moles]

Absorbance of proteins at 280 nm takes place due to absorbance of side chains of tryptophan, tyrosine and cysteine. Each of these side chains have their own extinction coefficients, all of which need to be added to find out the total extinction coefficient of a given protein.

Extinction coefficient of tryptophan = 5500 M-1cm​​-1

Extinction coefficient of tyrosine = 1490 M-1cm​​​​-1

Extinction coefficient of cysteine = 125 M-1​​​​cm​​-1

​​​​​​In BSA, number of tryptophan(W) residues = 2, number of tyrosine(Y) residues = 19, number of cysteine (C) = 35

So total molar extinction coefficient of BSA (\varepsilon) = 2 x 5500 + 19 x 1490 + 35 x 125 = 43685 M-1cm​​-1

Thus absorbance of BSA = \varepsilon cl = 43685 x (2.27 x 10-5) x 1 = 0.991

1.5 mg/ml BSA will have an absorbance of 0.991 at 280 nm.

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