Biological Functions of Peptides
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Questions and Answers

What do peptides serve as precursors of?

  • Antibiotics and antitumor agents
  • Amines like histamine and proline
  • Purines, pyrimidines, and vitamins (correct)
  • Hormones and neurotransmitters
  • Which amino acid protects living organisms against free radical induced damage?

  • Histidine
  • Proline (correct)
  • Cysteine
  • Tryptophan
  • What biological functions do peptides have?

  • Being used as anti-tumor agents and antibiotics
  • Serving as precursors of hormones and purines
  • Detoxification reactions and neurotransmission (correct)
  • Regulation of cell cycle and apoptosis
  • Which of the following is NOT mentioned as a biological function of peptides?

    <p>Protecting against free radical induced damage</p> Signup and view all the answers

    Peptides are involved in which of the following processes?

    <p>Detoxification reactions</p> Signup and view all the answers

    What is a common use of peptides?

    <p>As anti-biotics and antitumor agents</p> Signup and view all the answers

    What are the three main components that make up an amino acid?

    <p>Amino group, carboxyl group, and an R group</p> Signup and view all the answers

    What is the function of the α-carbon in an amino acid?

    <p>It is the central carbon atom to which both an amino and a carboxyl group are attached</p> Signup and view all the answers

    Which category of amino acids includes Valine, Leucine, and Lysine?

    <p>Essential amino acids</p> Signup and view all the answers

    Which type of amino acids can be synthesized in the body but may not meet the body's requirements during growth or pregnancy?

    <p>Semi-essential amino acids</p> Signup and view all the answers

    What happens if essential amino acids are absent in the diet?

    <p>It may adversely affect growth</p> Signup and view all the answers

    How do non-essential amino acids differ from essential amino acids?

    <p>Non-essential amino acids can be synthesized in the body, while essential amino acids cannot</p> Signup and view all the answers

    What is the term used to describe molecules that exist in two optically active asymmetric forms?

    <p>Enantiomers</p> Signup and view all the answers

    At what pH does the basic amino group in free amino acids typically have a pKa value?

    <p>Between 9 and 10</p> Signup and view all the answers

    What is the term used for compounds like amino acids that can act as both an acid and a base?

    <p>Amphoteric</p> Signup and view all the answers

    Why is it essential to note that amino acids found in proteins almost always possess only the l-configuration?

    <p>For optical activity</p> Signup and view all the answers

    When do free amino acids exist largely as dipolar ions or zwitterions?

    <p>At physiological pH (around 7-7.4)</p> Signup and view all the answers

    What is the significance of the isoelectric point of zwitterions?

    <p>It signifies when amino acids are electrically neutral</p> Signup and view all the answers

    Study Notes

    Structure and Classification of Amino Acids

    • Amino acids are organic molecules consisting of a basic amino group (―NH2), an acidic carboxyl group (―COOH), and an organic R group (or side chain) that is unique to each amino acid
    • The term amino acid is short for α-amino [alpha-amino] carboxylic acid
    • Each molecule contains a central carbon (C) atom, called the α-carbon, to which both an amino and a carboxyl group are attached

    Classification of Amino Acids

    • Essential amino acids: cannot be synthesized in the body and must be present in the diet (e.g., Valine, Isoleucine, Leucine, Lysine, Methionine, Threonine, Tryptophan, and Phenylalanine)
    • Semi-essential amino acids: can be synthesized in the body, but the rate of synthesis is lesser than the requirement (e.g., Arginine and Histidine)
    • Non-essential amino acids: synthesized in the body, and their absence in the diet does not affect growth (e.g., Glycine, Alanine, and other remaining amino acids)

    Chirality

    • All amino acids except glycine are chiral molecules, existing in two optically active asymmetric forms (enantiomers) that are mirror images of each other
    • Amino acids found in proteins almost always possess only the L-configuration

    Acid-Base Properties

    • Amino acids have both a basic and an acidic group at the α-carbon, making them amphoteric
    • Basic amino group has a pKa between 9 and 10, while the acidic α-carboxyl group has a pKa close to 2
    • At physiological pH (about 7–7.4), free amino acids exist largely as dipolar ions or “zwitterions”

    Biological Role of Amino Acids

    • Amino acids serve as building blocks of proteins
    • Some amino acids are found in free form in human blood
    • Peptides have many important biological functions, including:
      • Hormones
      • Antibiotics and antitumor agents
      • Detoxification reactions
      • Neurotransmitters
      • Regulation of cell cycle and apoptosis

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    Description

    Explore the various biological functions of peptides, including their role as precursors of hormones, vitamins, and neurotransmitters. Learn about peptides' significance in detoxification reactions, regulation of cell functions, and protection against free radical damage.

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