Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
20 Cards in this Set
- Front
- Back
- 3rd side (hint)
Three types of transport proteins?
|
Channels, Transporters, ATPase pumps
|
|
|
Channels
|
single file flow, continuous but specific & often gated
|
|
|
Transporters
|
one factor at a time via conformational change of protein. rate of diffuse slower than channel
|
|
|
ATPase pumps
|
ACTIVE transport via direct hydrolysis of ATP. (against conc. gradi)
|
|
|
Three types of Transporters
|
Uniporter, Symporter, Antiporter
|
|
|
Uniporter
|
one factor across membrane
|
|
|
Symporter
|
simultaneously 2 in same direction
|
|
|
Antiporter
|
simultaneously transports two in diff directions
|
|
|
P class pumps
|
tetrameres, two regulatory & two passage; ion pumps
|
|
|
F class pumps
|
in mitochondria membrane, used in ATPase synthesis, thru oxidative phospho & krebs you pump H ions out of mito matrix increasing Hions out. This brings neg charges, creating energy storage (capacitor)
|
Major info = reverse ATPases, use something going through to make ATP, also used in chloroplasts
|
|
V class
|
hydrolyzing ATP to drive ions through, pumping H into cells, relevant to lysosomes pumping H ions to lysosomes making them neg (but lysos use other prots to keep H from binding neg charges)
|
|
|
ABC Superfamily
|
consists of two transmembrane domains, two cytoplasmic ATP binding domains. Two examples include MDR1/CFTR1
|
|
|
MDR1
|
MultidrugResistantProtein - ATPase excretes hydrophobic compounds. Many toxins & drugs are hydrophobic, so detoxifies BUT also excretes drugs.
|
|
|
CFTR1
|
Differs from ABC family in two ways; 1 Functions as channel, not ATPase pump 2 Has regulatory domain, which has to be P'd by cAMP in addition to ATP hydrolysis. Significant in cystic fibrosis...
|
|
|
E1&2 states apply to which groups?
|
Transporters & P class ATPases
|
|
|
E1 =
|
Resting state conformation, high affinity site open
|
|
|
E2 =
|
closes high affinity site, opens low aff site - when factor is translocated to low site it is easily released
|
|
|
Binding mechanism for P class ATPases?
|
slightly differ by having separate ATPase domain for binding/hydrolyzing ATP. P from ATP to t-port protein forcing E1->E2 shift, factor translocates, dephosphs occurs and shift back to E1/release factor from low aff site
|
|
|
Na/K ATPase used for?
|
Electric potential & Na/K gradients; 3Na+ export: 2K+ imported for every ATP hydrolyzed
|
|
|
Pseudomonas aeruginosa
|
opportunistic bacteria associated with CF pts, lung infections etc
|
|