IB Biology SL Topic 2 — Proteins & Their Structure Paper 1 & 2 Core idea ~10 min read

How Proteins Form

Every amino acid has exactly the same middle. Same central carbon, same amino group, same carboxyl group, same lone hydrogen. Only one corner is different — the R group. Twenty versions of that one corner are enough to build enzymes, antibodies, hair, muscle and haemoglobin. This page is about how those units lock together.

📘 What you need to know

Why proteins matter so much

Genes code for proteins, and proteins do the work. Almost every reaction that keeps you alive depends on one. Here is the range:

The shape of one amino acid

Learn this once and it never changes. A central carbon with four things attached, and only one of them varies.

Every amino acid is built to this plan only the R group changes from one amino acid to the next R GROUP: the variable side chain R C N H H C H O OH AMINO GROUP —NH₂, behaves as a base CARBOXYL —COOH, acidic central (alpha) carbon R can be a single H (glycine) or a whole ring (phenylalanine) Four things on one carbon, and three of them are the same in all 20. The R group decides whether an amino acid is acidic, basic, polar or non-polar.
If a molecule in an exam has both an amino group and a carboxyl group on the same carbon, it is an amino acid. That is the identification test.
Notice that the amino acid carries an acidic group and a basic group at the same time. That is why R groups matter later: some are acidic, some basic, some polar, some not — and those differences are what fold the finished chain into a shape.

Making the peptide bond

Line two amino acids up so the carboxyl group of the first faces the amino group of the second. Then three atoms leave: an —OH from the carboxyl group and an —H from the amino group. Together they are H2O.

What is left behind is a carbon (still carrying its double-bonded oxygen) bonded straight to a nitrogen. That C—N link is the peptide bond, and it is covalent, so it is strong.

The reaction to learn amino acid + amino acid  →  dipeptide + H2O
Three atoms leave, one bond forms an OH from one amino acid, an H from the other AMINO ACID 1 AMINO ACID 2 its carboxyl end its amino end loses —OH loses —H + the R groups take no part CONDENSATION water is released DIPEPTIDE C N O H peptide bond + H₂O one water per bond To spot a peptide bond, find a nitrogen bonded to a carbon that has a double-bonded oxygen. The R groups sit off to the side and are never involved in forming the bond.
This is the same condensation reaction you met with sugars and fats. Different groups react, different bond name, identical idea.

🧩 How to draw a peptide bond in three steps

  1. Draw the two amino acids side by side. Line them up the same way round, so amino acid 1’s carboxyl group faces amino acid 2’s amino group.
  2. Circle the atoms that will leave. The —OH from the carboxyl group and one —H from the amino group. Two hydrogens and one oxygen, which is exactly H2O.
  3. Join the C to the N and write the water molecule as a separate product. Keep the double-bonded oxygen on that carbon — it does not go anywhere.

Dipeptides, polypeptides and going backwards

Essential and non-essential amino acids

Of the 20 amino acids, your cells can build 11 from other amino acids — these are the non-essential ones. The remaining 9 cannot be made in the body, so they have to come from food. Those are the essential amino acids.

What the syllabus actually asks. You are not expected to name them. You need to know that 9 of the 20 must come from the diet, that meat contains all nine, and that a plant-based diet needs a range of different foods to supply all nine.
“Essential” here does not mean more important. All 20 are needed. It simply means essential in the diet, because your body cannot make them.

Worked examples

WORKED EXAMPLE

Eight amino acids join to form a single polypeptide chain. State the number of peptide bonds formed and the number of water molecules released. [2]

Step 1: count the gaps, not the units 8 − 1 = 7 peptide bonds Step 2: one water per bond Every peptide bond is made by one condensation reaction. 7 peptide bonds and 7 water molecules Same rule as every other polymer: n monomers, n − 1 bonds.
WORKED EXAMPLE

Three amino acids with relative molecular masses of 75, 89 and 117 join to form a tripeptide. Calculate its relative molecular mass. [2]

Step 1: add the amino acids 75 + 89 + 117 = 281 Step 2: subtract the water lost 3 amino acids means 2 peptide bonds, so 2 waters leave. 281 − (2 × 18) = 281 − 36 = 245 Relative molecular mass = 245 Two bonds, not three. Count the gaps between the three units.
WORKED EXAMPLE

Describe how a peptide bond is formed between two amino acids. [3]

Point 1 A hydroxyl group is removed from the carboxyl group of one amino acid. Point 2 A hydrogen atom is removed from the amino group of the other amino acid; these leave as water. Point 3 The carbon of the first amino acid bonds covalently to the nitrogen of the second, in a condensation reaction. C bonds to N, water released Naming the two groups involved is worth more than saying “they join together”.

💡 Exam tip

⚠ Common mix-up

Up next: The Variety of Proteins — how just 20 building blocks give a number of possible proteins so big it may as well be infinite, and what some of the famous ones actually do.

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