Exam 1 Flashcards
The rough ER makes ?
Integral proteins, extracellular peripheral proteins, and secretory proteins
Ex. Insulin, immunoglobins
Insulin is made in the rough or smooth ER?
Rough ER
Insulin is a secretory protein
Sarcoplasmic Reticulum is found in?
Skeletal and cardiac muscle
Where is calcium stored?
Calcium is stored in cells in a structure called the sarcoplasmic reticulum.
The sarcoplasmic reticulum (SR) is a form of smooth muscle endoplasmic reticulum (ER) found in skeletal and cardiac muscle that functions as a regulator of Ca2+ storage and releases homeostasis during and after muscle contraction
Mitochondrial DNA ( mDNA) contains how many genes?
- 37 genes
- Many code for proteins involved in oxidative phosphorylation
Which organelle makes target specific vesicles?
Golgi complex
Which organelle degrades proteins, nucleic acids, sugars and lipids?
Lysosomes
Where is the site of rRNA synthesis?
Nucleus
Which protein filament is made up of actin proteins?
Microfilaments
Which proteins filament assist in muscle contraction?
Microfilaments
Which protein, (actin or tubuli), is the smallest and most abundant?
Actin
Which proteins filament provide structure and shape to eukaryotic cells?
Microtubules
Tubulin proteins polymerize into long chains or filaments called ?
microtubules
Cilia and flagella, projections from the cell, are made up of?
microtubules
What are the three types of cytoskeletal elements?
- Intermediate filaments ( strength and space fillers)
- Microfilaments (cell movement)
- Microtubules ( maintain shape and are transport paths in intracellular transport)
T/F Do muscle cells undergo continued mitosis?
FALSE
Muscle cells do not undergo continued mitosis.
They are Permanent cells.
Labile cells are?
Cells that regenerate frequently ( hours to days )
Ex. Skin and GI tract
Cells that replicate only when needed ( years to entire life) are called?
Stable cells
Ex. Liver and the proximal tubules of the kidney.
“Irreplaceable cells” ( entire life of individual)
Ex. Brain,skeletal, and RBC
Permanent cells
RBC have a lifespan of 120 days? Correct. Per Dr. V, “we are programmed with a certain amount, kind of like women have a set amount of eggs when they’re born. That’s all you get.”
Phospholipids are made up of?
Glycerol heads and 2 FA tails
Na+-K+ pump is an example of type of CM transport?
Primary active transport
(3 Na+ out and 2 K+ ions in making inside MORE negative)
Because the transport process uses ATP as an energy source, it is considered an example of primary active transport.
Cytolysis is due to which type of tonicity?
Hypotonic
outside environmenti has a lower concentration of solutes relative to the cytosol –> water moves in
Cell shrinks due to which type of tonicity?
Hypertonic
outside environmenti has a higher concentration of solutes relative to the cytosol –> water moves out
Substrate level phosphorylation occurs in the ?
Cytoplasm aka the soup
non-oxidative process –> no oxygen needed
What three metabolic phases make up cellular respiration?
Glycolysis, the Krebs cycle, and the electron transport chain
Oxidative metabolism ( 02 needed) consist of what two processes?
ETC ( electron transport chaing) and the Krebs cycle (citric acid cycle)
Preferred use of energy?
Glycogen
Where is glycogen stored?
In the liver and skeletal muscles.
What are the 3 major substrates in metabolism?
Glycogen (preferrred use of energy), Fats and Protein (least preferred for energy)
Glycolysis has a net gain of ___ATP molecules and ____NADH molecules?
2 Net ATP
2 NADH gained
What competes with calcium, blocking binding sites of Ca2+ and leading to muscle fatigue?
Lactic Acid
Pyruvate——————–>Lactate/Lactic Acid
Lactic Acid Fermentation
Deficiency in which cellular respiration enzyme leads to “inborn errors of metabolism”?
Pyruvate dehydrogenase deficiency
(enzyme responsible for the conversation of pyruvate to acetyl Co-A)
Pyruvate ———>acteyl Co-A
(Pyruvate dehydrogenase AKA PDH occurs in the matrix once pyruvate is shuttled inside)
FYI Pyruvate carboxylase deficiency and pyruvate dehhrogenase deficiency are the MCC of pyruvate metabolism disorders
What are the symptoms of pyruvate dehydrogenase deficiency in a new born?
N/V, respiratory problems, neuro delays, intellectual disability, underdeveloped corpus callosum and premature atrophy of cerebral cortex due to lactic acidosis
Sx start shortly after birth
One cycle of the Krebs cycle produces ___NADH, ___GTP, ____FADH2 AND ____CO2.
3 NADH
1 GTP
1 FADH2
2 CO2
**Cycle repeats 2x per glucose molecule!!