MCM_Final_TBL7 Flashcards

(83 cards)

1
Q

Extra Cellular Matrix is compised of…

A
  1. polysaccharide bound proteins
  2. spingolipids
    • keep cell hydrated and protected
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2
Q

protruding structures

A
  • connect cells together or
  • serve specialized functions
    • ex) villi
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3
Q

what lines the membrane?

A
  1. receptors
  2. other protein
  3. lipid rafts
  • (help to illict the function of pumps)
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4
Q

where is the basement layer?

A
  • located bellow the extra cellular matrix
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5
Q

which cystolic organelles are on the nucleus side of cell?

A
  1. rough ER
  2. mitochondria
  3. free ribosomes
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6
Q

which cystolic organelles are on the cell memebrane side of the cell?

A
  1. smooth ER
  2. peroxisomes
  3. golgi
  4. lysosomes
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7
Q

protein secretion

what is the path of an endogenous protein?

A
  • transcription and translation –> ER –> golgi –> destination
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8
Q

plasma membrane and secretions

(ex of some cellular secretions…)

  1. salivatory gland secretes …
  2. mucosal gland secretes …
  3. pancreas secretes …
  4. nerve neuron secretes …
A
  1. saliva via liquid
  2. mucus via liquid
  3. digestive zymogens via secretory glands
  4. neurotransmitters via vesicles
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9
Q

endoplasmic recticulum

A
  • two types
  • made up of interconnect flat sacs called cisternae
  • pathway: gene –> mRNA –> peptide
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10
Q

Rough ER

A
  • studded on exterior
  • functions:
    1. starts the synthesis of exported proteins
    2. makes proteins for other organelles (i.e lysomome proteins)
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11
Q

Smooth ER

A
  • smooth and near… generally closer to the membrane side of cell bc of its r_ole in metabolic functions_
  • Functions:
    1. stores G6P: sugar fate (decides if glucose leaves of stays in the cell)
    2. steroid hormone: estrogen
    3. detoxification: liver enzymes
    4. plasma membrane maintenance
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12
Q

Golgi

A
  • functions: protein modification and sorting

takes proteins from ER:

  1. sorts proteins by destination
  2. can add futher chemical modifications (O-glycan, start N-glycan)
    • barcode (ex is M-6-P)
  3. packages into vesicles for transport
  4. membrane LIPID maintenance
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13
Q

Transport Proteins: COPII goes …

A

from ER to Golgi (anterograde/forward)

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14
Q

Transport Proteins: Clatherin…

A
  • forms later vesicles for export (anterograde/forward)
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15
Q

Transport Proteins: COPI goes…

A

Golgi to ER (retrograde/backwards)

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16
Q

__________ + __________ transport proteins initiatie the process of ____________ of vesicles

Two pathways are (1) (2)

A
  • COPII + Clathrin transport proteins initiatie the process of exocytosis of vesicles
  1. constitutive secretory pathway (released immediately and is default of cells)
    • ex) pancreas —> digestive emzymes
    • lymphocytes
  2. regulated secretory pathway (stored in vesicles and needs a signal to bind to receptor before it secretes)
    • ex) neuron —> neurotransmitter
    • insulin, histamine, hormones
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17
Q

endocytosis

A
  • takes into the cell and the mechanism is DEPENDENT ON SIZE
    • immune cells use phagocytsis (repsonse)
    • duodenum cells use transporters (carb intake)
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18
Q

mitochondria

A
  • double membrane organelle, essential for metabolism
  • contains its OWN small circular DNA

Functions:

  1. ATP production via TCA, Oxidative Phosphorilation (ETC), B-Oxidation
  2. cell fate: apoptosis
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19
Q

Lysosomes

A
  • cell DIGESTION and RECYCLING
  • low pH to DENATURE biomolecules
  • contains many HYDROLASE enzymes that function at low pH
  • IMPERMEABLE membrane to enzymes
  • made from GOLGI
  • can FUSE with organelles and plasma membrane
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20
Q

Functions of Lysosomes (1-4)

A
  1. RECYCLES biomolecules to generate monomers or units for export
  2. AUTOPHAGY: organelle recycling through fusion (lysosome will fuse with mitochondria to for cell to make new mitochondria)
  3. MOVE LIPIDS between plasma membrane and golgi via FUSION
  4. G-6-P STORED HERE (glycolysis)
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21
Q

peroxisomes

A
  • involved in oxidative digestion and from ER

Functions: contian oxidative enzymes

  1. B-oxidation of VERY LONG FA
  2. A-oxidation of BRANCHED CHAIN AA
  3. AA oxidase
  4. oxidative SYNTHESIS of BILE & CHOLESTEROLE
  5. has to catalase to eliminate H2O2
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22
Q

Zellweger Spectrum Disorders

A
  • errors** in the **formation of peroxisomes with different severity due to PEX genes
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23
Q

Zellweger Syndrome

A
  • MOST SEVERE
  • very low peroxisome formation
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24
Q

Infant Refsum Disease

A
  • due to lack of peroxisomes/beta-oxidation of VLCFA, the very long chain FA accumulate
  • leads to:
    • cranial abnormalities
    • seziures
    • vison/hearing loss
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25
The nucleus contains
1. nuclear **envelope** (membrane) * entry in/out regulated by *nuclear* *pores* 2. **nucleolus** is the dark area where * **FUNCTIONAL RNAs** (ribsome, tRNA, small RNAs) are _transcribed and assembled_ 3. **heterochromatin** (DNA site)
26
Nuclear Envelope
* envelope allows _mRNA out_ *ONLY WHEN* they are ready (i.e mature mRNA) or _proteins in_ that have the *correct ID* * **nuclear pore complexes** regulate traffic in or out​ * the _OUTER_ envelope IS THE **Rough ER** * **chromatin** (DNA) is BOUND to the INNER membrane
27
colchicine
* used in **karyotyping** * it is an **INHIBITOR** that arrests the cell in **METAPHASE** so that the _chromosome pairs_ can be easily _vizualized_
28
Karyotyping
* used to ***vizualize*** _LARGE chromosome changes_ (LCC). * 0.5% of all live births have LCC * 50% of first trimester **miscarriages** have LCC * 95% of **tumor** cells have LCC * **FISH Technique** * **changes** in **_length**_ & _**gene location_** can be detected with FISH * _stains_ the chromosome w/ antibodies to determine what part of _gene is mising_
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Chromosomes
30
Chromosomes
* large **helix** of DNA complised of _two strands and base pairs_ * wound by **histones** to f_orm *nucleosomes*_ * nucleosomes FOLD into _chromatin_
31
What is Metabolic biological signaling? What conditions does it need? (A-D)
* signalling that involves **altering ATP usuage** and allocations in a specific way (fear --\> ATP usuage via epinerphrine signaling) Needs: A) **Specific** for a given **situation** B) **Amplifies** (triggers more **ATP use**) C) **Integrates** (can turn on/off) D) **Timely** (local and shuts off)
32
Autocrine Chemical Signaling
* cell targets itself * signal molecule is created by the same cell who will use it * ex) immune cells
33
Signalling Across Gap Junctions (chemical signaling)
* bewteen two cells *connected* by a gap junction * ex) two neurons communicate via neurotransmitters
34
Paracrine Chemical Signalling
* a cell targets a nearby cell * **"local signaling"** * helps *synchronize tissue functions* * ex) hormones (Growth Factor Hormone), histamine
35
Endrocine Chemical Signaling
* a cell targets a DISTANT cell through the BLOODSTREAM * ex) horomes (Epinephrine)
36
Generic Steps of Metabolic Signalling Pathway (1-4)
1. **Resting** state 1. *primary ligand binds* and starts the patway 2. **Activation** of a *key enzyme* that generates a SECONDARY *_MESSAGE_ (uses **ATP**)* 3. a **SECONDARY** ***_MESSENGER_*** activates the *target protein* 4. 1 target protein will stop the cascade locally ex) 1 epinephrine signal will use 100,000 glucoses
37
GPCR (G-Protein Coupled Receptor) Mechanism: Step 1
* _**total** **OFF**_ state * GCPR is **phosphorylated** * **GDP** is **bound** to *Trimeric G-Protein* subunits (alpha, beta, gamma)
38
GPCR (G-Protein Coupled Receptor) Mechanism: Step 2
* signal will induce changes: 1. *phosphate* **OFF** the GPCR 2. the **ligand** can now **bind** 3. *G-Protein* and *GPCR* **attach** to each other 4. **GTP** is **exchanged**
39
GPCR (G-Protein Coupled Receptor) Mechanism: Step 3
* **alpha** subunit (of the trimeric protein) **disocciates** * triggers a *structure **change***
40
GPCR (G-Protein Coupled Receptor) Mechanism: Step 4 (⍺-subunit)
big picture: adenyl cyclase (AC) ---\> cAMP ---\> PKA ---\> target protein 1. G⍺-s **bind with adenyl cyclase** * AC is active and **makes cAMP** * energy consumption is increased 1 adenyl cyclase makes many cAMP
41
GPCR (G-Protein Coupled Receptor) Mechanism: Step 5 (⍺-subunit)
* cAMP frees Protein Kinase A * seperates catalytic domain from regulatory domains cAMP acivates many PKA
42
GPCR (G-Protein Coupled Receptor) Mechanism: Step 6 (⍺-stimulatory)
* target **proteins are phosphorylated** and activity of them change * each tissue has different target proteins with _different biological responses_ Protein Kinase A uses many ATP to make a huge biological response
43
GPCR ⍺-s Action + Signal Ligands and Use
* **stimulates** adenyl **cyclase** 1. **Glucagon** (**prevent** **low** blood **glucose** by *converting* liver stored _glycogen to glucose_) 2. **Epinephrine** to *regulate* metabolic enzymes
44
GPCR (G-Protein Coupled Receptor) Mechanism: (⍺-q)
big picture (ex is Acetylcholine) : A) PhosphoLipase Cβ + PIP 2 ---\> IP3 Bi) IP3 ---\> Protein Kinase C --\> target protein Bii) IP3 ---\> Ca2+ release ---\> calmoduline kinase activation **αq** _binds_ and _activates_ Phospholipase C-Beta (**PLC β)**, which _cleaves_ PhosphatIdylinositol bisPhosphate (**PIP2**) _into_ diacylglycerol and Inositol triPhosphate (**IP3**), and _mediates_ the _activation_ of **Proetin Kinase C and Calmoduline Kinase II**.
45
GPCR ⍺-i Action + Signal Ligands and Use
* **inhibits** adenyl **cylase** 1. **serotonin (**relaxes you) 2. **cannabis (**relaxes you**)**
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GPCR ⍺-q Action + Signal Ligands and Use
* **activates** PL**Cβ** 1. **epinephrine** (_fear_) 2. **acetylcholine**
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GPCR ⍺s & GPCR ⍺i are...
* on/off pair * paired action is called **signal integration**
48
GPCR Signaling Bacterial Infection: **Cholera**
* *vibrio cholerae =* **cholera toxin** or **toxin**-coregulated **pilus** * symptoms: * voluminous rice water **diarrhea** * caused by c_ontaminated drinking water_ * **gram-negative** ***bacteria (***peptidoglycan sanwhich between membranes, so hard to see i.e negative) _use flagella_ to **bypass** the **mucosal** lining of the **intestines**
49
GPCR Signaling Bacterial Infection: **Whooping Cough**
* *Bordetella pertussis =* **pertussis toxin/ adenylate cyclase toxin** * _activates_ AC by **INHIBITING G⍺i** * symptoms: * **coughing** and progressive whooping symptoms * **eliminated** by **DTaP** vaccination
50
In what ways are GPCR signals terminated? (1-3)
1. **phosphodiesterase** DEGRADES _cAMP ---\> AMP_ or _GTP ---\> ​ GDP_ * therefore, you will see AMP in metabolic pathway when SIGNAL IS OFF 2. **phosphorylation** one of the target proteins is an enzyme that forces GPCR into a totally inactive state 3. **β-arrestin** will _bind to GPCR_ and *prevent* the G-protein complex from forming (**desensitization**) * causes _endocytosis of GPCR_ through **clathrin,** which will retrograde GPCR back to the lysosome for recyling
51
cytoskeleton are...
* mesh of **filamentous** elemens called: 1. microtubles 2. microfilaments 3. intermediate filaments (actin) * function: * **structural** stability for cell shape * important for cell **movement and rearrangement** of cytoplasmic components
52
microtubule structure
* **thickest**; vary in length with **hollow lumen** * **dense** wall made of **tubulin heterodimers (⍺-t**ubulin & **β-t**ubulin) * tubulin heterodimers _arrange in chains_ called **profilaments** that align _parralel_ to make walls * **13 profilaments** = one microtubule
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Microubules & Dynamic Instability
* exist in a state of **dynamic instability** (undergoing abrupt changes in legth through *polymerization* and *depolymerization*) * each microtubule is **_polarized_** with: * **+ end**: site of growth/**polymerization** * **- end**: site of shrinkage/**depolymerization**
54
Dynamic Instability Mechanism
1. **GTP-loaded tubulin subunits** *_initiate_* _polymerization_ 2. GTP **hydrolysis** changes the profiliment from tublin-_GTP structure to tubulin-GDP sturcture_ * growing microtubulines maintain a **cap** of tubulin-GTP _to keep straight_ * shrinking end characterized by fountain-like arrays 3. cycle _complete by exchange GDP from the shrinking_ products with GTP
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catastrophe
* transition from _growth to shrinkage_ in microtubule
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rescue
* transition from _shortenting to growth_ in microtubule
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Microtubule Organizing Center (MTOC)
* **initation (origin)** of the microtubule "microtubule nucleation" * contains **gamma-tubulin** * the starting point for assembly
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Microtubule Functions (1-4)
1. maintenance of **cell shap**e and **structure** 2. **transportation** of vesicles and organelles in cytoplasm 3. organization of **cilia** and **flagella** 4. formation of the **mitotic spindle** during cell division 1. **Taxol (Paclitaxel)** will _**permanently stabilize** microtubles_ and lead to *cell death* (useful for **cancer treatment** and hindering rapid cell growth in G1 phase)
59
Microfilaments (Actin-Filaments) Structure
* thinnest and flexible * consists of _**two** intertwing (**helical**) strands_ of **globular** proteins * **F-actin** = intact microfilaments * **G-actin** = unpolymerized/unassembled protein subunits * **powered by ATP hydrolysis** to form * hydrolysis of _ATP --\> ADP_ = destabilation/_depolymerization_ of the microfilament * **most abundant protein** in mammal cells
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Treadmilling
* **dynamic** movement in **microfillaments** * in **actin** filaments, _one end grows while the other end shrinks_ resulting in the filament seemingly "moving" across the cytosol
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Formin Protein
* promotes treadmilling in actin * promotes the _elongation of pre-existing_ actin filaments
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Profilin
* actin binding protein * involved in the **assembly** of the actin cytoskeleton
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Cofilin
* actin binding protein * involved in the **disassembly/shrinking** of the actin cytoskeletona
64
ARP2/3 Complex
* actin binding protein * involved in **branching** of the actin cytoskeleton
65
Microfilaments Function
* cell **organization** * establish **cell polarity** * core of actin filaments provides **microvilli** in intestins
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Contracticle Ring
**actin** plays an important role in **cell divison**: causes the _cell to stop moving_ and _orients/guides_ the microtubles of the *_mitotic spindles_* * the contracile ring = actin microfilament * seperates the daughter cells during *cytokinesis*
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Adehsion Belt
* microfillament * **maintains** the **structure** of _epitelial cell_ by a **belt** of _actin_ fillaments * _links_ the cytoskeleton of _adjacent cells_
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Stereocilia
* uses **_actin_** filament _rigidity_ to **sense vibration** * found on the surface of the **inner ear**
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Actin-Myosin
* **actin** serves as a track for a MOTOR protein called **myosin** * sliding of actin & mysosin = **muscle contractions**
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Cell Crawlling
* cells need to **move** in *repsonse to **stimuli*** * ​migration of white BC toward wound sites to fight infection * movement is assisted by **actin filaments** of the cytoskeleton of the cells
71
Cytochalasin-B (Anti-fungal Drug)
* **depolymerizes actin** filaments and *prevents cell crawling movement*
72
Phalloidin Toxin found in Death Cap Mushrooms (*Amanita phalloides)*
* **stabilizes actin PERMANANTLY** and *prevents cell crawling movement*
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Intermediate Filaments
* **rope** like * **toughest** and ***most durable*** * *CRITICAL* for maintaining **_cell shape and structure_** * abundant in cells that are subjected to **mechanical stress often** (*skin, connective tissue, and muscle cells*) * though _microtubules/fillaments_ help, they _break easily_
74
Intermediate Filaments Structure
* *two* COILED strands form **dimer** * _dimer_ will _stack_ to form **tetrameter** * **8 tetrameters = 1 filament**
75
Type I & II Intermediate Filaments
* **keratin**: forms the tissues of the **hair, skin, nails** * **protects** outside of the skin **against abraisions** and sticks cells together
76
Type III Intermediate Filaments
1. **Vimetin** * found in FIBROBLASTS (make XtraCell Matrix + collagen), ENDOTHETIAL cells, and LEUKOCYTES (White BC) 2. **Desmin** * found in MUSCLE cells 3. **Glial Fibrillary Acidic Factor** (**GFAP**) 1. found in ASTROCYTES ( a type of glial/glue cells that help neurons in the CNS/BRAIN)
77
Type IV Intermediate Filaments
* **neurofillaments**: subunirs of the _major_ intermediate _filaments_ of _neurons_
78
Type V Intermediate Fillaments
* **Lamins**: forms **NUCLEAR lamina** inside the nuclear **_envelope_** * provides **structural support** for the nucleus * assists with **CHROMATIN organization**
79
GFAP
* TYPE III intermediate filament * can be used for the **IDENTIFICATION of *brain tumor***
80
Molecular Motor Proteins: Function and Types (1-3)
* use **ATP hydrolysis** to ***move* cell cargo** (proteins, organelles, etc) _along_ the **_cytoskeletal filaments_** * _​**attach**_ to *cargo* with one end & to *microtubules/actin* with the other end Main Types are: 1. **Dynein** 2. **Kinesin** 3. **Myosin**
81
Axonal (Axoplasmic) Transport
* **movement** of *_cell cargo_* **to and from a neuron cell body through the axoplasm** (cytoplasm of its axon) * driven by **molecular** **motors** that run on **microtubule** track * neurons: specialized nerve cells that transmit nerve impulses
82
Anteriograde versus Retrograde Transport
* **Kinesin = (+) end** of microtubule **= Anterograde** * **Dyenein = (-) end** of microtube **= Retrograde**
83