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Biomolecules · Bioelements and biomolecules

Proteins

No other family of biomolecules has such a wide variety of functions as proteins: a collagen fibre, an antibody and a digestive enzyme are, at heart, the same kind of polymer folded in different ways. This section explains how a linear sequence of amino acids ends up determining a precise three-dimensional shape, and why that shape is, quite literally, the function.

Before you start, make sure you know: Gene expression (4th ESO)

Amino acids and the peptide bond

Spider silk, the keratin in hair and haemoglobin have opposite mechanical and chemical properties, yet when they are hydrolysed in the laboratory they all break down into exactly the same set of 20 simple molecules. What common architecture do these building blocks share that allows them to join together and produce such different functions?

General structure of an amino acid: the central α carbon bonded to an amino group, a carboxyl group, a hydrogen atom and a variable R group Cα α carbon NH₂ amino group COOH carboxyl group H hydrogen R (variable) side chain Condensation of two amino acids: the carboxyl group of the first loses an OH and the amino group of the second loses an H; water is formed and a dipeptide is left, joined by a C–N peptide bond H₂N C H R₁ C O OH + H N H C H R₂ C O OH –OH of the carboxyl –H of the amino amino acid 1 amino acid 2 condensation H₂N C H R₁ C O N H C H R₂ C O OH + H₂O peptide bond rigid C–N, no free rotation water released (OH + H) dipeptide
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What are amino acids and how many different types make up the proteins of living organisms? State which chemical groups all amino acids share and which endows each one…

What are amino acids and how many different types make up the proteins of living organisms? State which chemical groups all amino acids share and which endows each one with its particular properties.

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Name four different functions of proteins in living organisms and give a specific example of a protein for each function.

Name four different functions of proteins in living organisms and give a specific example of a protein for each function.

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What is a peptide bond? State between which chemical groups of the amino acids it forms and what molecule is released in the reaction.

What is a peptide bond? State between which chemical groups of the amino acids it forms and what molecule is released in the reaction.

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The four levels of structure

The four levels of protein structure: the primary is the sequence of amino acids joined by peptide bonds; the secondary, the α helix and β sheet with hydrogen bonds; the tertiary, the three-dimensional folding with a disulfide bridge; and the quaternary, the joining of four subunits, as in haemoglobin 1. Primary structure Met Gly Ser Leu Lys Cys Val H₂N COOH peptide bond amino acid sequence 2. Secondary structure α helix β sheet H bonds between –NH and –CO 3. Tertiary structure S–S 3D folding interactions between R groups 4. Quaternary structure α₁ β₁ β₂ α₂ several subunits e.g. haemoglobin (2 α + 2 β)
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Look at the diagram of the levels of protein organization, numbered from 1 to 4. Name each level, briefly describe its main feature, and give an example of a protein…

Look at the diagram of the levels of protein organization, numbered from 1 to 4. Name each level, briefly describe its main feature, and give an example of a protein that exhibits level 4.

G V L A S 1 2 3 4
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Functional adult hemoglobin ($\text{HbA}$) is a soluble heterotetramer. In sickle cell anemia, a point mutation in the $\beta$-globin gene replaces a glutamic acid with…

Functional adult hemoglobin ($\text{HbA}$) is a soluble heterotetramer. In sickle cell anemia, a point mutation in the $\beta$-globin gene replaces a glutamic acid with valine at position 6 of the polypeptide chain ($\text{HbS}$), causing deoxyhemoglobin to polymerize into long insoluble fibers that deform erythrocytes.

  1. a) Based on the chemical properties of the side chains of both amino acids, justify why this change in primary structure alters the conformation and solubility of the protein, and indicate what type of weak molecular interactions stabilize these fibers.
  2. b) In a genetic screening, two alternative mutations are detected at that same codon 6 of $\beta$-globin:
  • Variant A: glutamic acid is replaced by aspartic acid ($\text{Glu6Asp}$).

  • Variant B: glutamic acid is replaced by leucine ($\text{Glu6Leu}$).

Predict with reasoning which of these two variants will maintain a biological function virtually identical to healthy $\text{HbA}$ and which will cause pathological aggregation similar to sickle cell anemia.

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Denaturation: when shape is lost

When you squeeze lemon juice onto warm milk, the soluble casein precipitates into dense lumps, and when you fry an egg the liquid, transparent white turns opaque and solid in a few seconds. Why does a change in the surroundings alter the properties of a protein so radically without breaking its chain of amino acids?

Animation of the process of protein denaturation: the folded native chain shakes with heat or pH, gradually unwinds and changes from blue to purple until it becomes the unfolded chain; the chain stays whole and then folds back up to repeat. folded (native) heat / pH unfolded
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Haemoglobin loses its three-dimensional shape if the temperature or pH strays too far from normal values. What is this process called, which bonds are broken, and what…

Haemoglobin loses its three-dimensional shape if the temperature or pH strays too far from normal values. What is this process called, which bonds are broken, and what consequence does it have on the protein's function?

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Enzymes: biological catalysts

A commercial hydrogen peroxide solution takes months to break down in its bottle, but if you add a drop of blood or a piece of raw potato, the release of oxygen gas is instant and turbulent. How do cells manage to speed up a chemical reaction millions of times without being used up in the process?

Energy profile of a reaction: the enzyme lowers the activation energy (Eₐ) between reactants and products without changing their energy level reaction progress energy Eₐ Eₐ without enzyme with enzyme reactants (substrate) products Eₐ = activation energy
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What is an enzyme? Explain how it accelerates a chemical reaction with reference to activation energy and the enzyme-substrate complex.

What is an enzyme? Explain how it accelerates a chemical reaction with reference to activation energy and the enzyme-substrate complex.

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A patient with severe malnutrition is admitted to the emergency department with muscle weakness, disorientation, and severe lactic acidosis (symptoms compatible with…

A patient with severe malnutrition is admitted to the emergency department with muscle weakness, disorientation, and severe lactic acidosis (symptoms compatible with beriberi). Biochemical tests show elevated plasma concentrations of pyruvate and lactate, along with a sharp drop in cellular ATP despite normal glucose levels. Urgent administration of thiamine (vitamin B1) reverses the symptoms.

  1. a) Knowing that thiamine is the precursor of the coenzyme thiamine pyrophosphate (essential for the pyruvate dehydrogenase complex), explain what a coenzyme is and biochemically justify why its absence blocks cellular respiration and triggers lactate synthesis.
  2. b) If concentrated glucose saline had been infused into the patient to "give him energy" before administering the vitamin, his acidosis would have rapidly worsened. Justify this statement based on carbohydrate metabolic pathways.
  3. c) Since coenzymes are not consumed stoichiometrically in the reactions they catalyze (they are regenerated), reason why humans require a continuous dietary intake of water-soluble vitamins rather than a single lifetime dose.
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In a biochemistry laboratory, the thermal stability of an intracellular human enzyme is investigated. Aliquots of the enzyme are incubated for 20 minutes at four…

In a biochemistry laboratory, the thermal stability of an intracellular human enzyme is investigated. Aliquots of the enzyme are incubated for 20 minutes at four different temperatures ($15\ \text{°C}$, $37\ \text{°C}$, $45\ \text{°C}$, and $70\ \text{°C}$). Each sample is then divided into two fractions:

  • Fraction 1: its catalytic rate is measured immediately at the same temperature at which it was incubated.

  • Fraction 2: the sample is returned to $37\ \text{°C}$, kept for 15 minutes, and its catalytic rate is then measured at $37\ \text{°C}$.

The results show that Fraction 1 has optimal activity at $37\ \text{°C}$, very low activity at $15\ \text{°C}$, and zero activity at $70\ \text{°C}$. In Fraction 2, the sample pretreated at $15\ \text{°C}$ recovers $100\ \%$ of its maximum activity, whereas the one pretreated at $70\ \text{°C}$ maintains an activity of $0\ \%$.

  1. a) Interpret molecularly the results of Fraction 2 for the $15\ \text{°C}$ and $70\ \text{°C}$ samples, distinguishing between the kinetic energy of the system and protein denaturation.
  2. b) Predict how the curve for Fraction 1 would change if an equivalent enzyme purified from the thermophilic bacterium Thermus aquaticus ($T_{\text{optimum}} \approx 75\ \text{°C}$) were used, and justify what adaptations in the bonds of its tertiary structure allow it to be functional at that temperature.
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Cofactors, saturation and enzyme inhibition

A cofactor is a non-protein component needed by some enzymes: it can be an ion, such as Mg²⁺ or Zn²⁺, or an organic molecule, called a coenzyme. Many vitamins are precursors of coenzymes; they do not supply energy, and taking more does not guarantee more enzyme activity. The apoenzyme together with its functional cofactor forms the holoenzyme.

As the substrate increases with a fixed amount of enzyme, the initial rate rises until it approaches a maximum rate: the active sites become saturated. A competitive inhibitor occupies the active site; its effect can be reduced by increasing the substrate. In pure non-competitive inhibition the maximum rate decreases and adding substrate does not restore it.

Graph of rate against substrate with saturation, and diagrams of an enzyme with no inhibitor, with a competitive inhibitor and with a pure non-competitive inhibitor Vmax (saturation) V′max Initial rate (v) Substrate concentration [S] No inhibitor Competitive Pure non-competitive substrate No inhibitor inhibitor Competitive inhibitor Pure non-competitive

Summary

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