A-level Chemistry/WJEC/Module 4/Peptides

Amino Acids are an important class of organic compounds that contain both the amino (-NH2) and carboxyl (-COOH) groups. Of these acids, 20 serve as the building blocks of proteins. Here is a list of the "standard" amino acids, with some of their systematic names: alanine ((2S)-2-AminoPropanoic acid) arginine asparagine aspartic acid ((2S)-2-AminoButaneDioic acid) cysteine ((2R)-2-Amino-3-SulfanylPropanoic acid) glutamic acid ((2S)-2-AminoPentaneDioic acid) glutamine glycine (AminoEthanoic Acid) histidine isoleucine ((2S, 3S)-2-Amino-3-MethylPentanoic acid) leucine ((2S)-2-Amino-4-MethylPentanoic acid) lysine ((2S)-2,6-DiAmino-Hexanoic acid) methionine phenylalanine proline serine ((2S)-2-Amino-3-HydroxyPropanoic acid) threonine ((2S, 3R)-2-Amino-3-HydroxyButanoic acid) tryptophan tyrosine valine ((2S)-2-Amino-3-MethylButanoic acid) 19 of the 20 are constructed according to a general formula: H2NCHRCOOH As the formula shows, the amino and carboxyl groups are both attached to a single carbon atom, which is called the alpha carbon atom. For this reason, these are known as alpha (α) amino acids. Attached to the carbon atom is a variable group (R); it is in their R groups that the molecules of the 20 standard amino acids differ from one another. In the simplest of the acids, glycine, the R consists of a single hydrogen atom. Other amino acids have more complex R groups that contain carbon as well as hydrogen and may include oxygen, nitrogen, or sulfur, as well. Proline has an unusual structure where the R group is also attached to the amine, forming a cyclic structure and making it the only secondary amine in the standard amino acids. thumb|upright=2|The 20 amino acids specified by the genetic code. thumb|upright=0.4|left|Leucine is a typical amino acid, with a primary amine group. thumb|upright=0.4|Proline is the only standard amino acid with a secondary amine group. When a living cell makes protein, the carboxyl group of one amino acid reacts with the amino group of another to form a peptide bond. The carboxyl group of the second amino acid similarly reacts with the amino group of a third, and so on, until a long chain is produced. This chainlike molecule, which may contain from 50 to several hundred amino acid subunits, is called a polypeptide. A protein may be formed of a single polypeptide chain, or it may consist of several such chains held together by weak intermolecular bonds. Each protein is formed according to a precise set of instructions contained within DNA — the genetic material of the cell. These instructions determine which of the 20 standard amino acids are to be incorporated into the protein, and in what sequence. The R groups of the amino acid subunits determine the final shape of the protein and its chemical properties; An extraordinary variety of proteins can be produced from the same 20 subunits. Proteins have roles such as enzymes (e.g. amylase, pepsin), hormones (e.g. insulin), receptors (e.g. the insulin receptor) and structural fibres (e.g. silk and keratin). thumb|centre|upright=1.5|Oxytocin is a 9-amino acid peptide hormone which is involved in human social bonding, the beginning of childbirth and lactation. The standard amino acids serve as raw materials for the manufacture of many other cellular products, including hormones and pigments. In addition, several of these amino acids are key intermediates in cellular metabolism. Stereoisomerism The L-amino acid structures follow the "CORN" rule: Putting the H-atom at the front, and the CO, R and N groups behind the alpha-carbon, the CO-R-N groups follow a clockwise pattern. thumb|upright=0.7|The CORN rule for L-amino acids. The R/S notation is almost the same: The H-atom has lowest priority and is placed behind the alpha-carbon. The priorities are usually N > CO > R which are anticlockwise, and gives the (2S) designation. In cysteine, however, the R group contains sulfur so the priority is -NH2 > -CH2SH > -COOH and L-cysteine is designated (2R). Two amino acids have chiral centres in their sidechains; isoleucine (2S, 3S) and threonine (2S, 3R). Ionic forms in solution At neutral pH, amino acids exist in the form of zwitterions. The acid and amine groups essentially neutralise one another: H2NCHRCOOH ⇌ H3N+CHRCOO– At low pH, the amino acids accept a proton and become cations. At high pH, they release a proton and become anions: Low pH : H3N+CHRCOOH ⇌ H3N+CHRCOO– + H+ ⇌ H2NCHRCOO– + 2 H+ : High pH thumb|upright=3|center|Glycine at a range of pH values. The sidechains of several amino acids can donate or accept protons. Acidic amino acids are aspartic acid and glutamic acid. Basic amino acids are lysine, arginine and histidine. At neutral pH, the acidic amino acids tend to form anions and the basic amino acids tend to form cations. Dipeptides Two amino acids can combine in a condensation reaction to make a dipeptide: H3N+CHR1COO– + H3N+CHR2COO– → H3N+CHR1CO-NHCHR2COO– + H2O The reaction is usually shown without zwitterions: H2NCHR1COOH + H2NCHR2COOH → H2NCHR1CO-NHCHR2COOH + H2O Peptides are recorded, and synthesised naturally, in the sequence N to C. There is a second possible product in the reaction above: H2NCHR2COOH + H2NCHR1COOH → H2NCHR2CO-NHCHR1COOH + H2O center yes 3 File:Glycine-2D-skeletal.svg Glycine File:L-methionine-2D-skeletal.png Methionine File:Glycylmethionine.svg Dipeptide formed from the amino acids glycine and methionine File:Physiological Cysteine.svg Cysteine (zwitterionic form) File:Glycine-zwitterion-2D-skeletal.svg Glycine (zwitterionic form) File:L-Cysteinylglycin.svg Dipeptide formed from the amino acids cysteine and glycine, showing the zwitterionic form of the dipeptide. Primary Structure The primary structure of a protein is not really a structure, it is the sequence of amino acids that make up its polypeptide chain. The sequence is listed from the end of the polypeptide with free -NH2, to the end with free -COOH. This is the same way that the protein is assembled in living cells. H2NCHR1COOH H2NCHR1CO-NHCHR2COOH H2NCHR1CO-NHCHR2CO-NHCHR3COOH H2NCHR1CO-NHCHR2CO-NHCHR3CO-NHCHR4COOH The genetic code can specify 20 amino acids, so a dipeptide, with 2 amino acids, can have 202 = 400 possible primary sequences. A polypeptide with 99 amino acids could have 2099 = 6.34 x 10128 possible primary sequences. Most calculators can't calculate 2099 but there is a trick using the relationship between standard form numbers and log10. Note that log10(2099) = 99 x log10(20) = 128.8020. This means 2099 = 10128.8020 = 100.8020 x 10128 = 6.34 x 10128. One form of the enzyme α-amylase, from human saliva, has the 496 amino acid primary sequence: EYSSN TQQGR TSIVH LFEWR WVDIA LECER YLAPK GFGGV QVSPP NENVA IHNPF RPWWE RYQPV SYKLC TRSGN EDEFR NMVTR CNNVG VRIYV DAVIN HMCGN AVSAG TSSTC GSYFN PGSRD FPAVP YSGWD FNDGK CKTGS GDIEN YNDAT QVRDC RLSGL LDLAL GKDYV RSKIA EYMNH LIDIG VAGFR IDASK HMWPG DIKAI LDKLH NLNSN WFPEG SKPFI YQEVI DLGGE PIKSS DYFGN GRVTE FKYGA KLGTV IRKWN GEKMS YLKNW GEGWG FMPSD RALVF VDNHD NQRGH GAGGA SILTF WDARL YKMAV GFMLA HPYGF TRVMS SYRWP RYFEN GKDVN DWVGP PNDNG VTKEV TINPD TTCGN DWVCE HRWRQ IRNMV NFRNV VDGQP FTNWY DNGSN QVAFG RGNRG FIVFN NDDWT FSLTL QTGLP AGTYC DVISG DKING NCTGI KIYVS DDGKA HFSIS NSAED PFIAI HAESK L Secondary Structure In 1951 Linus Pauling (1901-1994) deduced, using models, that polypeptide chains could fold into two repeating structures, held together by hydrogen bonds. These regular structures are largely independent of the amino acid sidechains. Alpha helix Polypeptide chains can fold into a helical structure where the C=O of one peptide bond forms a hydrogen bond to the N-H of a peptide bond 4 amino acids further along the chain. This structure can repeat indefinitely. thumb|upright=0.5|A section of polypeptide, folded into an alpha-helix, showing the hydrogen bonds in red. The "ribbon" illustration is a common way to show the presence of an alpha helix. center yes 200 File:Polypeptide forming an alpha helix, with hydrogen bonds in magenta.gif A section of polypeptide, folded into an alpha-helix, showing the hydrogen bonds in magenta.]] File:KRT1 Structure with type 2 highlighted.png Keratin (the protein that makes hair, fingernails, etc) is made entirely of alpha-helices. Four polypeptide chains are shown here. Beta sheet Two or more polypeptide chains can fold into an extended structure where the C=O of one peptide bond forms a hydrogen bond to the N-H of a peptide bond on a second chain. The chains in the beta sheet can be loops of one polypeptide chain, or parts of entirely different chains. center yes 480 File:Beta sheet bonding parallel-color.svg Parallel beta sheet. The strands both run from top to bottom. parallel (also running from bottom to top) and the other is "antiparallel" - its chain runs from top to bottom. File:Beta sheet bonding antiparallel-color.svg Antiparallel beta sheet. The strand on the left runs bottom to top, the strand on the right runs in the opposite direction. center yes 200 File:Animated Beta sheet.gif Three polypeptide chains forming a beta sheet. Relative to the middle chain, which runs from bottom to top, one polypeptide is parallel (also running from bottom to top) and the other is "antiparallel" - its chain runs from top to bottom. File:Image of a protein backbone structure with MD simulation.png Spider silk protein is mainly beta-sheet. Tertiary Structure The full 3D structure of a protein is called its tertiary structure. The secondary structures are folded together by a combination of hydrophobic interactions, dipole-dipole forces, ionic bonds and (sometimes) covalent bonds. Hydrophobic interactions are where non-polar amino acid sidechains tend to be buried in the centre of the protein, away from the surrounding water. center yes 300 File:Salivary alpha-amylase 1SMD.png Human salivary alpha-amylase structure, showing its alpha helices and beta sheets. There is a single polypeptide chain, coloured from blue (N-terminus) to red (C-terminus). Calcium and chloride ions are shown as yellow and green spheres, respectively.]] File:Alpha-amylase.gif Alpha-amylase wireframe model, showing every atom.