All Exams Test series for 1 year @ ₹349 only
Question

The C-terminal carboxyl group and the N-terminal amino group in amino acids have a dissociation constant ($pK_a$) of 2.2 and 9.2, respectively. The $pK_a$ of side chain carboxyl group in glutamic acid is 4.2 and side chain amino group in lysine is 10.2. The difference in isoelectric point ($pI$) of lysine and glutamic acid (rounded off to two decimal places) is ________.

Calculating $pI$ Difference: Lysine and Glutamic Acid

The isoelectric point ($pI$) is the pH at which an amino acid has no net electrical charge. It's calculated differently for standard, acidic, and basic amino acids based on their ionizable groups.

Calculating $pI$ for Glutamic Acid (Glu)

Glutamic acid is an acidic amino acid due to its side chain carboxyl group. The $pI$ is the average of the $pK_a$ values of the alpha-carboxyl group and the side chain carboxyl group.

  • $pK_a$ of alpha-carboxyl group = 2.2
  • $pK_a$ of side chain carboxyl group = 4.2

Calculation:

$pI_{Glu} = \frac{pK_{a(\text{alpha-COOH})} + pK_{a(\text{side-chain COOH})}}{2}$

$pI_{Glu} = \frac{2.2 + 4.2}{2} = \frac{6.4}{2} = 3.2$

Calculating $pI$ for Lysine (Lys)

Lysine is a basic amino acid due to its side chain amino group. The $pI$ is the average of the $pK_a$ values of the alpha-amino group and the side chain amino group.

  • $pK_a$ of alpha-amino group = 9.2
  • $pK_a$ of side chain amino group = 10.2

Calculation:

$pI_{Lys} = \frac{pK_{a(\text{alpha-NH}_3^+)} + pK_{a(\text{side-chain NH}_3^+)}}{2}$

$pI_{Lys} = \frac{9.2 + 10.2}{2} = \frac{19.4}{2} = 9.7$

Determining the $pI$ Difference

The difference between the isoelectric points of lysine and glutamic acid is calculated as follows:

Difference = $|pI_{Lys} - pI_{Glu}| = |9.7 - 3.2| = 6.5$

The difference in the isoelectric point ($pI$) of lysine and glutamic acid is 6.5.

Was this answer helpful?

Important Questions from Chemical Biology {p}K_a Isoelectric Point

  1. Consider the two $pK_a$ values of valine as 2.32 and 9.62. The isoelectric point (pI) of this amino acid is __________. (rounded off to two decimal places)
  2. The $pK_a$ values of the carboxylic and amino groups of an amino acid with a non-ionizable side chain are 2.17 and 9.13, respectively. The isoelectric point (rounded off to two places of decimals) of this amino acid is ________.
  3. Consider the given peptide, Ala-Glu-Val-Asn-Ile-Asp-Pro-Asp-Gln-Gly-Asp. The net charge on the peptide at pH 1.0 will be ________
  4. Considering that the three pKas of histidine are pK$_1$=1.8, pK$_2$=9.2 and pK$_R$=6.0, its isoelectric point will be _____ (rounded off to one decimal place).
  5. An amino-acid has one proton donating group in the side chain (R). The $pK_{COOH}$, $pK_{NH2}$ and $pK_R$ values for this amino-acid are 2.19, 9.67 and 4.25, respectively. Which one of the following statements about this amino-acid is CORRECT?
Need Expert Advice?

Start Your Preparation with Prepp Mobile App

Download the app from Google Play & App Store
Download the app from Google Play & App Store
Prepp Mobile App