Eukaryotic cell structure and function Flashcards

1
Q

What is life

A

The state or quality that distinguishes living beings or organisms from inorganic matter

Metabolism
Response
Sensitivity
Growth
Reproduction
Excretion
Nutrition

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2
Q

What are cells

A

fundamental units of life

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3
Q

What defines a cell?

A

• Discrete, easily recognisable packages (cell membranes)
• made up of phospholipids which prevent the entry of hydrophilic compounts

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4
Q

What are the chemical properties of cells?

A

• all cells are similar inside
• they are composed of the same sort of molecules
• information flows from DNA via RNA to proteins
• proteins influence cell behaviour

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5
Q

What is the composition of cells?

A

• 70% water
• 30% varying chemicals and proportions of structural and functional molecules

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6
Q

Give physical properties of prokaryotic cells and examples

A

• eg spherical cells, rod shaped cells, spiral cells

• typically spherical, rod like or corkscrew shaped
• protective cell wall surrounding plasma membrane
• no organelles, circular DNA
• typically single celled, aerobic or anaerobic

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7
Q

What are the physical properties of eukaryotic cells?

A

• Larger and more complex than prokaryotes
• can be unicellular or part of multicellular organisms
• linear DNA molecules
• chromosomes in nucleus, chromosome number and ploidy widely variable
• membrane bound organelles

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8
Q

What are the functions of the plasma membrane

A

• Regulate transport (eg nutrients, waste)
• Maintain ‘proper’ chemical conditions
• Provide a site for chemical reactions unlikely to occur in aqueous environment
• Detect signals in the extracellular environment
• Interact with other cells or the extracellular matrix

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9
Q

Role of Nucleus

A

membrane bound structure, separates DNA from cytosol, transcription from translation (see genetics)

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10
Q

role of endoplasmic reticulum

A

RER: protein synthesis

SER: lipid and steroid synthesis

Ca2+ ion storage & detox

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11
Q

role of ribosomes

A

50% protein and 50% rRNA

used for protein synthesis, often associated w RER

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12
Q

role of golgi complex/apparatus

A

series of flattened discs called cisternae, modifies and sorts most ER products

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13
Q

role of mitochondria

A

Site of ATP production via aerobic metabolism, important role in apoptosis, self replicating (fission)

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14
Q

What are the properties of mitochondrial DNA?

A

• Mitochondria contains multiple mtDNA molecules
• genes in mtDNA exhibit cytoplasmic inheritance and encode rRNAs, tRNAs, and some mitochondrial proteins
• the size and coding capacity of mtDNA varies considerably in different organisms
• products of mitochondrial genes are not exported
• mutations in mtDNA cause several genetic diseases in humans

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15
Q

role of lysosomes

A

•degrade certain cell components, material internalised from the environment
• appear
as electron dense bodies on EM
• single membrane
• pH of lumen 3.5-5
• contains acid hydrolases
• if lysosomal enzyme is missing eg hydrolytic enzymes (generic defect): accumulation of material leads to lysosomal storage disease

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16
Q

role and features of peroxisomes

A

role:
• responsible for degrading:
- fatty acids eg oxidation of them
- toxic compounds eg alcohol oxidation

features:
- single membrane
- contain oxidases (eg urate oxidase and catalase)
- can be diverse in size and enzyme composition eg special plant peroxisomes

17
Q

composition of cytoskeleton

A

3 major filamentous compounds:
• microtubules ~25nm (tubulin)
• actin filaments ~6nm (actin)
• intermediate filaments ~10nm (different subunit proteins)

18
Q

role of cytoskeleton

A

• Essential in movement of cellular components and the cell itself
-maintains cell shape
-vesicular transport
-cell division

• Number of accessory proteins associated with with the filamentous components

19
Q

function of actin

A

• maintains cell shape by resisting tension (pull)
• moves cells via muscle contraction or cell crawling
• divide animal cells into two
• move organelles and cytoplasm in plants, fungi, and animals
• cell shape and whole cell locomotion
• cells which need to move rich in actin

20
Q

function of intermediate filaments

A

• maintain cell shape by resisting tension
• anchor nucleus and some other organelles
• rope like fibrous proteins (defined by size)
• abundant cytoplasmic and nuclear proteins
• provide structural reinforcement and stress resistance

21
Q

function of microtubules

A

• maintain cell shape by resisting compression
• move cells via flagella or cilia
• move chromosomes during cell division
• assist formation of cell plate during plant cell division
• move organelles
• provide tracks for intracellular transport
• dynamic (end grows rapidly)

22
Q

What are motor proteins

A

(not enough to have cytoskeleton)
• need motors to move vesicles
• three superfamilies identified with multiple members
• presence of conserved amino acids sequence, forms the ATP-binding and force-producing motor domain

23
Q

What does the motor protein Myosin do

A

acts on actin- cell surface contractions- morphological changes- vesicle motility- muscle cell contractions

24
Q

what does the motor protein Dynein and kinesin do?

A

Interact with microtubles to move vesicles and organelles, movement of flagella and cilia- essential in mitosis and meiosis in function of the spindle

25
Q

What are the physical properties of myosin?

A

• expressed in virtually all eukaryotic cells
-couple hydrolysis of ATP to conformational changes

• head (motor domain)
- ATP and actin binding site
- exhibits actin activated ATPase activity

• Neck region
- an extended a helix

• Tail region
- effector domain
- determines specific function

26
Q

What are the properties of Dynein and Kinesin?

A

• cytoplasmic motors:
- Dynein: large mass, higher complexity, activity can be dynamically regulated
- Kinesin: simpler structure, either active or inactive

• both move in one direction only
- dynein: moves towards - end of microtubule
- kinesin: move towards + end of microtubule
- force and movement generated by ATP hydrolysis

•involved in many processes (eg cell division, intracellular transport)

27
Q

What mutations in the cytoskeletal components can lead to disease?

A

• actin mutations: congenital myopathy
• intermediate filament mutation: >30 human disease
• microtubule mutations/disfunction : neurodegeneration

28
Q

How do we use cytoskeleton as a target?

A

•Pharmaceutical agents can be used to target cytoskeletal components
- eg polymerisation of filaments
- colchicine, causes microtubule depolymerisation, may contribute to its role in treating gout

•targeting cancer
- vinca alkaloids and paclitaxel disrupting cell cycle progression by inhibiting mitotic microtubules

• can also target assessory proteins, and ECM
- integrins are target for antiplatelet drugs