Proteins Flashcards

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1
Q

What are some functions of proteins?

A

-Enzymes to catalyze synthesis of carbohydrates in mitochondria
-Structure of an organism
-Structures that move individual cells, large cargo, or molecules within cells
-Cell-cell signalling
-Antibodies to destroy viruses and bacteria

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2
Q

What is the nucleus

A

Contains DNA, has a double membrane

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3
Q

What is the nucleolus

A

produces and assembles ribosomes and transcribes rRNA

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4
Q

Describe the nuclear envelope

A

-Non fluid
-Contains nuclear pore complexes to move material in and out (RNA, enzymes, DNA building materials)
-Double membrane

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5
Q

Where are ribosomes located

A

-In cytosol
-Attached to endoplasmic reticulum

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6
Q

How do amino acids bond to form polypeptides

A

-Formed by condensation or broken by hydrolysis
-Peptide bonds between carboxyl and amino groups of 2 amino acids

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7
Q

What determines amino acid properties and 3D folding shape

A

Side chains

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8
Q

What is a primary structure

A

Simple sequence infromation

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9
Q

What are the 2 secondary structures

A

Alpha helix
-Amino and carboxyl groups attached by peptide bonds
-Coiled by hydrogen bonds between carbonyls and carboxyls

Beta Pleated Sheet
-Parallel protein strands with hydrogen bonds between carboxyl and amino groups of adjacdent strands

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10
Q

What is a tertiary structure

A

3D shape formed by bonds between R groups

Shape formed by secondary structures and side chain interactions

Contains hydrogen bonds, van der waal interactions, covalent and ionic bonds, disulfide bonds, hydrophobic interactions

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11
Q

What assists with protein folding

A

Molecular chaperones
-Bind to hydrophobic regions and prevent incorrect folding

Chaperonins
-Molecule complexes that act as isolation chambers for a forming polypeptide

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12
Q

What is a quaternary structure

A

Assembly of polypeptide subunits that form the final functional protein

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13
Q

What is found in the endomembrane system

A

Nuclear envelope, endoplasmic reticulum, lysosomes, gilgi apparatus

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14
Q

How does a polypeptide enter the endoplasmic reticulum lumen

A

-Sequence causes ribosome to attach to ER
-It binds a signal recognition particle which then binds to a SRP receptor in the ER membrane
-The polypeptide then goes through a channel into the lumen

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15
Q

What is glycolysation

A

The addition of carbohydrate chains which helps with protein stability, folding, and cell-cell recognition

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16
Q

Which proteins end up in the cell membrane

A

porins and receptors

17
Q

Which proteins exit the cell

A

Antibodies, hormones, enzymes

18
Q

How do proteins get to their destinations

A

Tags allow them to be transported a certain way (often by transport vesicles) and released

19
Q

What are plasmids

A

Circular Prokaryotic DNA containing 1 or 2 genes that replicate independently and transfer between cells

20
Q

Describe Fred Neufeld experiment

A

Observed virulent (S) and non-virulent (R) strains of streptococcus pneumoniae, s-strain produces a smooth carbohydrate coating that masks the bacteria from the immune system and r-strain does not

21
Q

Describe Frederick Griffith experiment

A

Heated and exploded virulent bacteria leaving macromolecules intact, mixed exploded s-strain with r-strain and it resulted in death. Therefore, r-strain transformed into virulent strain

22
Q

Desccribe Avery McCarty, MacLeod experiment

A

Made heat killed virulent strain samples, added r-strain to each with a different enzyme that would destroy a particular molecule.
By process of elimination, mouse lived when DNA was destroyed therefore DNA is the hereditary material

23
Q

What defines non-polar side chains

A

-Hydrophobic
-Includes hydrocarbon chains or benzene
-Ex. Alanine, valine, leucine, isoleucine, methionine, phenylalanine, tryptophan, tyrosine

24
Q

What defines a polar side chain

A

-Hydrophilic
-Can form H-bonds
-ex. lysine, arginine, histidine, aspartic acid, glutanic acid, asparagine, glutamine, serine, threonine

25
Q

What is a monogenic disease

A

Caused by a mistake in 1 gene (ex. cystic fibrosis)

26
Q

Symptoms of cystic fibrosis

A

-cough
-wheezing
-thick mucus
-respiratory infections
-constipation
-salty sweat
-Impacts lungs and digestion

27
Q

DIfference between healthy and CF airways

A

Healthy: movement, pink colour, cartilage, clear mucus, capillaries

CF: Inflammed capillaries, narrow airways, thick yellow mucus (must be removed through aspiration to prevent infection)

28
Q

What causes cystic fibrosis symptoms

A

Incorrect unbalanced transport of ions and water across the cell membranes, resulting in maany ducts being compromised

29
Q

How do ciliated cells work

A

Sweep in the same direction, covered by airway surface liquid, undercurrent sweeps mucus upwards. ASL must be the height of the cilia

30
Q

What is the genetic cause of cystic fibrosis

A

-Deletion mutation in CFTR protein causing frameshift
-Protein can not fold, should be a protein channel but sometimes does not make it out of ER to function in cell membrane

31
Q

What is the cystic fibrosis transmembrane conductance regulator protein

A

-Channel protein
-Moves chloride ions across epithelial membranes into ASL and regulates Na ions brought into cell
-Creates balanced ASL liquid height
-If built incorrectly, ER holds it back