J.R. S. answered 09/12/22
Ph.D. in Biochemistry with an emphasis in Neurochemistry/Neuropharm
I'm pretty sure that we'd need the pI for lysine, or at the very least, the pKa values for the ionizable groups.
These values will vary depending on the source one uses, but here are values from one source:
pKa COOH = 2.2
pKa NH3 = 9
pKa NH3 side chain = 10.5
pI given = 9.8
pI calculated = (9 + 10.5) / 2 = 9.75
At pH = pKa1= 2.2, there would be an equal amount of dicationic (COOH, NH3+, NH3+) and monocationic form (COO-, NH3+, NH3+).
As the pH increases above 2.2, there will be more monocationic (COO-, NH3+, NH3+) compared to the dicationic (COOH, NH3+, NH3+) form .
At pH =pKa2 = 9.0, there will be an equal amount of the monocationic (COO-, NH3+, NH3+) form and zwitterion (COO-, NH3+, NH2)
At pH above 9.0, there will be more COO-, NH2, NH2
Calculation of the molarity of the different forms requires using the Henderson Hasselbalch equation.
pKa = pH + log [HA] / [A-]