Cell Structure & Intracellular Organelles: An Overview Flashcards

1
Q

nucleus

A

largest organelle, most cells have 1, however, skeletal muscle have >1 and RBCs have 0.
Contains the cell’s DNA complexed with histone proteins to form chromatin.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

nucleosome

A

complex of 8 molecules of histones around which DNA is wound, appears as beads on a string. Fundamental subunit of chromatin.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

heterochromatin

A

highly condensed DNA-protein complex, DNA is inaccessible to transcription factors, and thus is “silent” in this configuration (DNA methylated and histones deacetylated)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

euchromatin

A

less condensed DNA-protein complex, DNA is accessible to transcription factors and thus is transcriptionally active. (DNA demethylated and histones acetylated)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

nucleolus

A

most prominent structure within nucleus, site of rRNA trancription, pre-rRNA processing and ribosome subunit assembly
***Cells that are active in protein synthesis such as liver cells and some highly proliferative cancer cells have increased numbers of these.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

nuclear pores

A

small, protein-lined openings in the nuclear envelope that allow for exportation of RNAs and ribosomes from nucleus to cytosol, as well as importation of transcription factors

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

mitochondria

A

organelle that converts PE from food into cellular energy under aerobic conditions, have a highly porous outer membrane and an inner membrane that is impermeable to many ions, including protons, and is convoluted, forming folds called cristae. Site of e- transport chain

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

mitochondrial diseases

A

genetic disease group that is passed down from mother to all children, variable disease symptoms/expression can occur in these diseases due to different mutation loads: can be different # mutations per organelle, different # organelles with mutations per cell, and different # cells with mutated organelles per tissue/organ system.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

ribosomes

A

protein synthesizing machinery of the cell, free scattered in the cytosol or bound to ER membrane. Made up of large and small subunits (Euks: 80S = 60S + 40S, Proks: 70S = 50S + 30S)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

80s, 60s, 40s

A

eukaryotic ribosomal subunits

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

endoplasmic reticulum

A

network of flattened sacs and branching tubules that extends throughout the cytoplasm, function to produce and process various proteins, lipids, toxins

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

rough ER

A

organelle covered in ribosomes, involved in production and processing of membrane-embedded and secretory proteins

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

smooth ER

A

organelle involved in production of lipids, detox of drugs and poisons, and calcium storage

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

golgi apparatus

A

organelle made up of several flattened, stacked sacs, referred to as cisternae. Considered the shipping and distribution center for the cell’s chemical products - modifies proteins and distributes things back to ER or out to cell membrane. Protein modifications here include: glycosylation, sulfation, phosphorylation, and proteolysis.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

cis

A

face of golgi apparatus where substances enter from the ER for processing

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

trans

A

face of golgi apparatus where substances exit in vesicles or lysosomes

17
Q

lysosome

A

organelle that is filled with hydrolytic enzymes, degrades intracellular molecules - primarily degrades extracellular proteins that were taken up by endocytosis or engulfed by autophagosomes. Lumen is acidic which activates the enzymes (hydrolases).

18
Q

peroxisomes

A

small organelles that contain enzymes linked to metabolic pathways such as beta oxidation of long-chain fatty acids. The enzymes use molecular oxygen to neutralize free radicals, releasing H2O2, which must be converted to H2O by catalase. (most abundant in liver cells)

19
Q

proteasomes

A

small cytoplasmic protein complexes degrade proteins, involved in the quality control of endogenously synthesized proteins by marking misfolded and denatured proteins for degradation, also degrades TFs, cyclins, and proteins encoded by viruses and intracellular pathogens.
**Uses polyubiquitination to tag for degradation.

20
Q

centrosome

A

consists of a bound pair of centrioles surrounded by a shapeless matrix of dense material. During cell division - directs migration of chromosomes to opposite ends of the cell (spindle apparatus). In non-dividing cells, centrioles attach to the inner side of the membrane to form a basal body - which forms a cilia/flagella or non-motile primary cilium.

21
Q

membrane asymmetry

A

negatively charged lipids are usually found on the inner leaflet of the plasma membrane while positively charged lipids are found on the outer leaflet. Disorganization of this usually indicates cell damage.

22
Q

flippases

A

one of the 3 protein families responsible for the generation, maintenance, regulation, and dissipation of lipid asymmetry in the plasma membrane; this protein moves lipids from the outer monolayer to the inner monolayer with the help of ATP (because this is against the gradient)

23
Q

floppases

A

one of the 3 protein families responsible for the generation, maintenance, regulation, and dissipation of lipid asymmetry in the plasma membrane; this protein moves lipids from the inner monolayer to the outer monolayer with the help of ATP (because this is against the gradient)

24
Q

scramblases

A

one of the 3 protein families responsible for the generation, maintenance, regulation, and dissipation of lipid asymmetry in the plasma membrane; this protein exchanges lipids between monolayers in either direction toward equilibrium, without the use of ATP.

25
Q

facilitated diffusion

A

movement of solutes bidirectionally from areas of low concentration to areas of high concentration; does not require ATP - going with its gradient; rate of diffusion can hit a max (saturation) at which point increased concentration of solute will not increase rate. Ex: channel proteins, carrier/transporter proteins

26
Q

channel proteins

A

form a pore in the cell membrane, highly specific for a particular ion, facilitate diffusion leading to equilibrium; can be always open, voltage-gated, ligand-gated, mechanically-gated.
*Due to finite # of these, there is a saturation pt at which increased concentration of substrate will not increase the rate of diffusion.

27
Q

transporter/carrier proteins

A

facilitate diffusion of molecules bidirectionally across a membrane by binding its substrate, inducing a change in shape that moves the bound molecule through the lipid bilayer
*Due to finite # of these, there is a saturation pt at which increased concentration of substrate will not increase the rate of diffusion.

28
Q

active transport

A

transport that requires ATP and is concentrative - meaning that the solute can be moved against its concentration gradient.

29
Q

primary active transport

A

directly uses ATP to drive transport of solutes across a membrane; frequently called pumps, ex: NA+/K+ pump kicks out 3 Na ions and lets in 2 K ions per cycle.

30
Q

secondary active transport (cotransport)

A

indirectly uses ATP to drive transport; uses electrochemical gradients generated by active transporters such as the Na/K pump as an energy source to move molecules against their gradient. Further divided into symporters and antiporters.

31
Q

symporter

A

secondary active transporter that moves both substrates in the same direction

32
Q

antiporter

A

secondary active transporter that moves its substrates in opposite directions

33
Q

other cellular roles of electrochemical gradients

A
  1. cell communication - ex: neurons use Na channel to allow influx of Na to enter cytosol, thus depolarizing neuron and allowing for signaling through the action potential
  2. regulate enzyme activity - ex: many enzymes require Ca2+ to work, cells can essentially turn enzymes on and off by opening calcium channels and increasing or decreasing cellular calcium concentration
  3. regulate cellular secretion - ex: insulin secreted by beta islet cells
34
Q

sodium potassium pump creates these 3 gradients

A
  1. Outside to inside Na+ gradient
  2. Inside to outside K+ gradient
  3. Inside cell negative membrane potential