DNA and proteins Flashcards

1
Q

What are proteins made of?

A

Amino acid chains known as polypeptide chains, coiled up forming its shape.

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2
Q

What are the four levels of structure of a protein?

A

Primary, secondary, tertiary, quaternary.

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3
Q

Describe the primary structure of a protein

A

The chain of amino acids/polypeptide chain. Considered useless at this stage.

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4
Q

Describe the secondary structure of a protein

A

Polypeptide chain begins folding as hydrogen bonds begin forming.
Still can’t do its job.

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5
Q

Describe the tertiary structure of a protein

A

Protein continues coiling further as different kinds of bonds begin forming.
Can maybe now do its job if it doesn’t require the quarternary stage.

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6
Q

Describe the quarternary structure of a protein

A

Some proteins have more than one polypeptide chain. This is where other coiled chains connect.
Haemoglobin is an example of this.
Protein can now do its job.

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7
Q

Define what an enzyme is

A

An enzyme is a biological catalyst

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8
Q

What are the two types of enzymes?

A

Anabolic - enzymes which are building larger complex molecules from simple simpler molecules.
ANTS are BUILDING nests

Catabolic - breaking down large complex molecules into smaller simpler molecules.
CATS are BREAKING things (pushing things off the edge)

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9
Q

Define what a gene is

A

A section of DNA which codes for one specific mRNA molecule

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10
Q

What is the active site of an enzyme?

A

The active site is where the job is done. Where substrates slot into the enzyme to either be broken down or built up.

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11
Q

What are inhibitors? and what are the two types?

A

Inhibitors turn the enzyme on and off as we don’t always need them on.
Inhibitors slow down a reaction, product is still made but just slower. (toxins are inhibitors).

Competitive inhibitors - Sitting in the active site stopping substrates from entering. Competing for the active site.

Non-competitive inhibitors - don’t sit in the active site, inhibitor finds the allosteric site and changes the shape of the active site. Substrate can no longer fit.

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12
Q

What are genetic mutations?

A

A mutation is any change in the codon sequence.

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13
Q

What are the different types of genetic mutations?

A

Substitution
- Nonsense
- Missense
- Silent
Frameshift
- deletion

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14
Q

What is a nonsense mutation?

A

When bond gets damaged by radiation or something else, and wrong letters get put together. Results in a stop codon in the middle of the mRNA strand.
Changes one amino acid.

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15
Q

What is a Missense mutation?

A

When wrong amino acid gets coded for. Still makes sense but the wrong sense. Can result in a change in the proteins shape.
Changes one amino acid.

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16
Q

What is a silent mutation?

A

No change, no big deal. Will change the codon (first letter) but will just change it into a degenerate, so does not actually change the amino acid coded.
Changes one amino acid.

17
Q

What is a deletion mutation?

A

Changes everything! One letter is taken out, so changes codons all the way down stream. This is almost always bad.
Changes everything.

18
Q

List three factors which increase chances in a mutation occurring.

A

High radiation
Mutagenic chemicals
Some viruses

19
Q

Define transcription

A

Using a section of of DNA (gene) to build a complimentary strand of mRNA.
Happens in the nucleus.

20
Q

Define translation

A

A strand of mRNA to provide the instructions for a ribosome to build a polypeptide chain.
Happens in the endoplasmic reticulum.

21
Q

Explain the lock and key theory

A

The enzyme’s active site is the lock/hole, substrate is the key.
The wrong key/substrate won’t fit into the lock/active site.
Can have one lock and multiple keys and they will all work. Lock doesn’t get used up.
Eventually the lock/active site may break.

22
Q

Describe protein synthesis

A

The process of transcribing an mRNA strand from DNA, and building a polypeptide chain/protein through the ribosome enzyme.

23
Q

What is SCNT? (Somatic Cell Nuclear Transfer)

A

When the nucleus from a somatic cell is placed into an enucleated gamete for cell division to begin.

24
Q

Explain the steps of SCNT

A
  1. Somatic cell’s nucleus is removed
  2. Nucleus is then injected into ovum from a second donor
  3. That egg can now initiate development through mitosis
25
Q

What is SCNT used for?

A

Cloning

26
Q

What is gel electrophoresis?

A

A technique used to seperate DNA fragments according to size

27
Q

Explain the steps of gel electrophoresis

A
  1. restriction enzymes cut up strands of DNA at certain spots, relating to DNA bases.
  2. DNA is placed in wells in the gel electro…. machine (in negatively charged side)
  3. When the machine is turned on the DNA begins moving through the gel (towards positive side)
  4. Shorter pieces move faster so will be closer to positive side than longer pieces.
  5. To see DNA the gel must be stained and put under a UV light
  6. Similarities in DNA will line up
28
Q

What is gel electrophoresis used for?

A

Testing relatedness between people (parents and children)

DNA fingerprinting (crime scenes)

29
Q

What is the formula for maths question

A

bases - introns / 3 - 1 = number of amino acids