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Moodle Access. MEDI12042011SU. Lecture 1. Amino Acids. The central Dogma of Biology. DNA bases: (A, G, C, T) RNA bases: (A, G, C, U) Protein: Amino acids (20). DNA: AAA GGA GAA TAG TGT GGC CAT CGT CGC RNA: UUU CCU CUU AUC AUA CCG GUA GCG Protein: F P L I I P V A A A
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Moodle Access MEDI12042011SU
Lecture 1 Amino Acids
The central Dogma of Biology DNA bases: (A, G, C, T) RNA bases: (A, G, C, U) Protein: Amino acids (20) DNA: AAA GGA GAA TAG TGT GGC CAT CGT CGC RNA: UUU CCU CUU AUC AUA CCG GUA GCG Protein: F P L I I P V A AA (Phe Pro Leu Ile Ile Pro Val Ala AlaAla)
Amino acids are building blocks of proteins • Amino acid consists of: • a central carbon atom (α-carbon) • an amino group, • a carboxylic acid group • a hydrogen atom • R group (side chain, distinguish the different amino acids). The key elements of an amino acid are: carbon, hydrogen, oxygen, and nitrogen.
α-carbon is asymmetric (has four different substituents) except for one amino acid (Glysine), for which the R group is a hydrogen atom. • Amino acids occur as enantiomers (non-superimposable complete mirror images). • L-amino acids are the naturally occurring enantiomers found in all proteins. • (L is for Life)
If objects are superimposable, it means you can not tell them apart. If they are non-superimposable, then you can always distinguish them (ex: Amino acids!).
Amino acid consists of: • a central carbon atom (α-carbon) • an amino group, • a carboxylic acid group • a hydrogen atom • R group (side chain, distinguish the different amino acids). Amino acids are usually classified by the properties of their side-chain
Hydrophobic amino acids,Mostly C atoms and H atoms in their side chain • Where in proteins? • Glysine, smallest amino acids, followed by Alanine! • Proline: R group is linked to the NH2+ , rigid five membered ring structure (imino group). • Methionine, one of two sulphur containing amino acids.
Non-polar aromatic R group Tryptophan is the bulkiest amino acid!
Non-Polar side Chains Hydrophobic Larger the Non-polar side Chain Higher is the hydrophibicity
Polar can be ionized and participate in polar interactions (ex. Hydrogen bonds)! • O or N in the side chain. • Where in proteins? • Cysteine, one of two sulphur containing amino acids! Carbonyl group and Amindgroup
Disulfide bonds Cysteine Cystine • R group of Cysteine contains a sulfhydryl group (-SH) • Two Cysteins can become oxidized to form a dimer. • Disulfide bond (-S-S-) is a covalent bond that stabilize many proteins.
(Acidic amino acids) Acidic amino acids arepolarand negatively charged at physiological pH. Both acidic amino acids have a second carboxyl group.
(Basic amino acid) H+ Histidine: weakly basic-uncharged at physiological PH= 7.4 Longest aa is Arginine, followed by lysine!
AA with polar side-chains are located in the surface of proteins. • AA with non-polar side-chains are located in the interior of proteins.
An essential amino acidor indispensable amino acidis an amino acid that cannot be synthesized de novo, and therefore must be supplied in the diet.
HA H+ + A- Weak Acid Proton Conjugate base [ H+ ] [ A- ] Ka = [ HA ] (acid ionization constant) Ionization of amino acids: when acids ionizes it produces the proton and the conjugate base! Acid ionization constant = Ka The larger the Ka, the stronger the acid (more able to dissociate)!
Rearrange Ka equation to get Henderson-Hasselbach Equation! [ A- ] pH = pKa + log [ HA ] [ H+ ] [ A- ] Ka = [ HA ] (acid ionization constant) Ka [ HA] [ H+ ]= [ A- ] Henderson-Hasselbach equation pKa = -log Ka
Example: Ka =0.5 (less ability to ionize) Ka=0.9 (more able to ionize) pKa = 0.3 pKa= 0.04 • The larger the Ka the stronger the Acid (more able to dissociate)! • The smaller the Ka the weaker the Acid (less able to dissociate)! • The larger the ka, the smaller the pka (more able to dissociate)! • The smaller the Ka, the larger the Pka (less able to dissociate)!
Charge: -1 Charge: +1 Pka=2 H 2 Pka=10 Charge: 0 (When aa have a net charged of zero its called a Zwitterion) PH=7 PH=1 PH=12 Adding a base Low PH High PH