4.7 - Amino Acids, Peptides and Proteins Flashcards

1
Q

What is an α-amino acid?

A

α-amino acids are organic molecules containing a carboxylic acid group and amine group bonded to the same carbon atom.

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2
Q

Give the displayed structure of an
α-amino acid, representing the side
chain with ‘R’

A
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3
Q

Which amino acid is the only amino acid that is not chiral?

A

Aminoethanoic acid (glycine):
The R group on aminoethanoic acid is just a hydrogen atom so the carbon is not bonded to 4 different groups.

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4
Q

Why are all amino acids (except glycine) chiral molecules?

A

All amino acids, except glycine, contain a chiral carbon atom bonded to four separate groups. It is bonded to an amino group, a carboxylic group, a hydrogen atom and an R group.

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5
Q

How are amino acids amphoteric?

A

Amino acids are amphoteric meaning they have both acidic and basic properties. This is because they have a basic amino group and an acidic carboxylic group.

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6
Q

What is a zwitterion?

A

A zwitterion is a dipolar ion which means it has a positive charge in one part of the molecule and a negative charge in another part of the molecule.

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7
Q

Give the general displayed structure of an amino acid zwitterion

A
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8
Q

What happens when an alkali is added to an amino acid zwitterion?

A

The NH3+ group donates a hydrogen ion to the OH- ions of the alkali to form water. The organic compound is no longer a zwitterion because it only contains a negative charge.

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9
Q

What happens when an acid is added to an amino acid zwitterion?

A

The COO- group accepts a hydrogen ion from the acid. The organic compound is no longer a zwitterion as it only contains a positive charge.

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10
Q

Give the general displayed structure of an amino acid in acidic conditions

A
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11
Q

Give the general displayed structure of an amino acid in alkaline conditions

A
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12
Q

Why do amino acids have relatively high melting points?

A

In the solid state, the zwitterion is the usual form that an amino acid exists in. This means there are strong ionic attractions between neighbouring zwitterions in the solid, so a large amount of energy is required to break the ionic attractions.

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13
Q

Explain the solubility of amino acids in water

A

Amino acids are generally soluble in water because strong ionic attractions form between the zwitterions and the polar water molecules.

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14
Q

How does a peptide bond form?

A

A peptide bond forms during a condensation reaction between two amino acids. A water molecule is lost.

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15
Q

What is the difference between a dipeptide and a polypeptide?

A

A dipeptide is formed from two amino acids while a polypeptide is formed from more than two amino acids.

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16
Q
A
17
Q

How do polypeptides lead to protein formation?

A

Polypeptides are chains of more than two amino acids joined together by peptide links. When the chain becomes very long, they can fold into proteins.

18
Q

What does the primary structure of a protein involve?

A

The primary structure of a protein is the sequence of amino acids which make up the polypeptide chain.

19
Q

What does the secondary structure of a protein involve?

A

The protein chain has peptide links which can form hydrogen bonds with with each other, leading to two possible shapes of the chain, known as the secondary structure:
- α-helix spiral
- β-pleated sheet
Both are stabilised by hydrogen bonding.

20
Q

What does the tertiary structure of a protein involve?

A

The tertiary structure relates to the extra bonds which can form between different parts of the polypeptide chain, determining how the α-coils or β-pleated sheets of the protein fold with respect to each other. The types of extra bonds include ionic and hydrogen bonds and disulphide bridges.

21
Q

Give examples of how proteins are essential for living systems

A
  • Proteins are important for structural functions in living organisms. Nails, feathers, skin and collagen are all made up of protein.
  • Enzymes are proteins that are biological catalysts that speed up chemical reactions in the body.
  • Some hormones are proteins, e.g. insulin.
22
Q
A