Proteins
When you chew a piece of bread or boiled yuca and leave it in your mouth for a while, you notice it starts to taste a little sweet. Nobody added sugar: a protein in your saliva, amylase, is cutting the starch. On the stove, egg white goes from liquid to white in seconds. In the hospital, a person with sickle cell anemia has red blood cells that become deformed. All of this has the same explanation: a protein's shape is its function. On this page you will see how proteins are built and what happens when that shape changes.
Amino acids and the peptide bond
The silk of a spider web, the keratin in hair, and the hemoglobin in blood are very different. Yet if we break them down in the lab, they all fall apart into the same set of 20 simple pieces. What do those pieces have that lets them join together and form such different things?
Think of amino acids as the letters of the alphabet: with just 20 letters you can write millions of different "words" (proteins). They all share the amino group and the carboxyl group; the R group is what gives each one its properties (some are charged, others repel water).
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.
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.
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.
The four levels of structure
A chain of amino acids does not stay stretched out like a thread: it folds until it takes on a precise shape. That shape is described in four levels, each built on the previous one.
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.
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.
- 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.
- b) In a genetic screening, two alternative mutations are detected at that same codon 6 of $\beta$-globin:
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Variant A: glutamic acid is replaced by aspartic acid ($\text{Glu6Asp}$).
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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.
Denaturation: when shape is lost
When you squeeze lemon into warm milk, it curdles into lumps. When you fry an egg, the transparent white turns white and solid. Why does a simple change in temperature or acidity transform a protein so much without breaking its chain of amino acids?
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?
Enzymes: biological catalysts
If you leave hydrogen peroxide in a bottle, it takes months to break down. But if you drop in a small piece of raw potato, it bubbles right away: oxygen pours out. How do cells speed up reactions millions of times without being used up?
Notice that the curve with the enzyme reaches the same final height. The enzyme does not change the reactants or the products; it only lowers the "hill" that has to be climbed.
Examples in digestion: amylase (saliva) cuts starch, pepsin (stomach) cuts proteins, and lipase digests fats. Each enzyme acts only on its own substrate, because its active site fits only that substrate.
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.
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.
- 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.
- 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.
- 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.
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:
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Fraction 1: its catalytic rate is measured immediately at the same temperature at which it was incubated.
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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 $0\ \%$.
- 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.
- 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.
Extension: saturation and enzyme inhibition
A cofactor is a non-protein component that some enzymes need: it can be an ion (Mg²⁺, Zn²⁺) or an organic molecule, the coenzyme. Taking more vitamins than necessary does not increase enzyme activity.
If the amount of enzyme is fixed and you increase the substrate, the rate rises until it approaches a maximum rate: all the active sites are occupied (saturation). A competitive inhibitor occupies the active site, and its effect is reduced by adding more substrate. A noncompetitive inhibitor binds at another site on the enzyme: it lowers the maximum rate and adding substrate does not fix it.