Amphoteric nature of aminoacids

7,276 views 15 slides May 18, 2016
Slide 1
Slide 1 of 15
Slide 1
1
Slide 2
2
Slide 3
3
Slide 4
4
Slide 5
5
Slide 6
6
Slide 7
7
Slide 8
8
Slide 9
9
Slide 10
10
Slide 11
11
Slide 12
12
Slide 13
13
Slide 14
14
Slide 15
15

About This Presentation

animation may not be visible. :(
Subscribe to my youtube channel for such great contents
www.youtube.com/c/AwesomeBiochemistry


Slide Content

Dr. Kalpeshkumar C Nakarani Tutor cum Second year Resident Amphoteric nature of Aminoacids

Zwitterion  At a specific pH the amino acid carries both the charges in equal number and exists as dipolar ion or ‘zwitterion’ At this point net charge on it is zero. Isoelctric pH ( pI )  The pH at which a molecule exists as a ‘zwitterion’ or ‘dipolar ion’ and carries no net charge is known as isoelectric pH ( pI ). pKa = pK of an acid = the pH at which the protonated and unprotonated species are present at equal concentration.

Amino acids bears at least two ionisable weak acid groups - COOH (Stronger acid) - NH 3 + (Weaker acid) R-COOH R-COO - + H + R-NH 3 + R-NH 2 + H + Acidic (Protonated form) Conjugate base ( Unprotonated form)

Titration of R-COOH (e.g. Acetic acid) pKa = 4.76

Titration of R-NH 3 + (e.g. Methylamine) pKa = 10.6

The perturbed p K a of glycine is caused by repulsion between the departing proton and the nearby positively charged amino group on the -carbon atom, as described in Figure . Similarly, the p K a of the amino group in glycine is perturbed downward relative to the average p K a of an amino group. This effect is due partly to the electronegative oxygen atoms in the carboxyl groups, which tend to pull electrons toward them, increasing the tendency of the amino group to give up a proton. Hence, the -amino group has a p K a that is lower than that of an aliphatic amine such as methylamine

The pI value can be calculated by taking the average pKa values corresponding to the ionisable group  

The aminoacids with an ionisable R group have more complex titration curve Aspartate Glutamate Lysine Arginine Histidine Tyrosine Cysteine

Titration curve of GLUTAMATE pK (COOH)=2.19 pK (R) = 4.25 pK (NH3) = 9.67 Structure at physiological pH

Titration curve of HISTIDINE pK (COOH)=1.82 pK (R) = 6.0 pK (NH3) = 9.17

Simply, How to find pI of the AA containing ionisable R-group? Write out all possible ionic structures, proceeding from strongly acidic to basic solution. Identify the isoionic / Zwitterionic representation (The species which bears no net charge) The pI is the pH at the midpoint between the pK values on the either side of the isoionic species

Thank You 
Tags