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BI5.1-9 | Chemistry & Metabolism of Proteins and Immunology — Practice Quiz

Practice 10 questions · Untimed · Unlimited attempts

Click any question card to reveal the correct answer.

Q1 BI5.1 1 pt

An amino acid that the human body cannot synthesise and must be obtained from the diet is classified as 'essential'. Which of the following is an essential amino acid?

A Glutamate
B Alanine
C Leucine
D Aspartate

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Q2 BI5.2 1 pt

A protein with quaternary structure consists of multiple polypeptide subunits assembled into a functional complex. Which of the following proteins has quaternary structure?

A Myoglobin
B Haemoglobin
C Collagen (single alpha chain)
D Insulin A-chain alone

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Q3 BI5.3 1 pt

In protein digestion, trypsinogen is an inactive zymogen secreted by the pancreas. Which enzyme activates trypsinogen to trypsin, and where does this activation occur?

A Pepsin, in the stomach
B Enterokinase (enteropeptidase), in the duodenum
C Chymotrypsin, in the jejunum
D Carboxypeptidase, in the ileum

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Q4 BI5.4 1 pt

Serum protein electrophoresis of a 65-year-old man with bone pain and recurrent infections shows a tall, narrow spike in the gamma-globulin region (M-spike). This pattern is most consistent with:

A Nephrotic syndrome
B Chronic liver cirrhosis
C Multiple myeloma
D Iron deficiency anaemia

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Q5 BI5.5 1 pt

Which class of immunoglobulin is the ONLY one that crosses the placenta, providing passive immunity to the newborn?

A IgA
B IgM
C IgG
D IgE

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Q6 BI5.6 1 pt

The urea cycle detoxifies ammonia in the liver. Which enzyme catalyses the rate-limiting step of the urea cycle, and where in the cell does it function?

A Arginase, in the cytoplasm
B Ornithine transcarbamylase, in the mitochondria
C Carbamoyl phosphate synthetase I (CPS-I), in the mitochondria
D Argininosuccinate synthetase, in the cytoplasm

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Q7 BI5.6 1 pt

A patient with advanced liver cirrhosis develops confusion, asterixis (flapping tremor), and elevated blood ammonia. Which mechanism BEST explains the brain toxicity caused by hyperammonaemia?

A Ammonia directly destroys neuronal myelin sheaths
B Excess ammonia combines with alpha-ketoglutarate to form glutamate, then glutamine, which accumulates in astrocytes causing osmotic swelling
C Ammonia inhibits the electron transport chain in neurons
D Ammonia converts haemoglobin to methaemoglobin, reducing oxygen delivery to the brain

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Q8 BI5.7 1 pt

A newborn screening test (heel-prick at 48 hours) reveals elevated phenylalanine levels. The baby is diagnosed with classical phenylketonuria (PKU). Which enzyme is deficient, and what is the mainstay of treatment?

A Tyrosinase deficiency; tyrosine supplementation
B Phenylalanine hydroxylase deficiency; low-phenylalanine diet with tyrosine supplementation
C Homogentisic acid oxidase deficiency; vitamin C supplementation
D Branched-chain alpha-keto acid dehydrogenase deficiency; leucine-restricted diet

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Q9 BI5.8 1 pt

A 4-day-old neonate develops jaundice with elevated unconjugated (indirect) bilirubin. The jaundice is physiological. Which of the following BEST explains physiological jaundice of the newborn?

A Excessive haemolysis due to Rh incompatibility
B Immature liver with low UDP-glucuronyl transferase activity
C Obstruction of the bile duct by a gallstone
D Deficiency of albumin to transport bilirubin

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Q10 BI5.9 1 pt

A patient is brought to the emergency department after exposure to a house fire. They are drowsy but have cherry-red skin colour. Pulse oximetry reads 98%. Which haemoglobin derivative is most likely responsible for this presentation, and why is pulse oximetry misleading?

A Methaemoglobin — pulse oximetry reads it as deoxyhaemoglobin
B Carboxyhaemoglobin (HbCO) — pulse oximetry cannot distinguish HbCO from oxyhaemoglobin
C Foetal haemoglobin (HbF) — it has higher oxygen affinity and mimics oxygenation
D Sulphaemoglobin — it absorbs light at the same wavelength as oxyhaemoglobin

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