OP: Regulation Flashcards
describe flow of electrons
the e- flows from the molecules w/ lower E0 to that w/ highest E0
E0
standard redox potential
difference in E0 is associated w/ gibbs nrg and they are inversely related
G = -nf(delta)E0
establishing a proton gradient
e- transfer thru the ETC leads to pumping H+ from matrix to innermemb space
2 factors cause the proton motive force (pmf) to drive ATP synthesis by complex V
pmf
proton motive force
- -the 2 factors involved that drive protons from matrix to inner memb space
- -also the chemiosmotic hypothesis
pH gradient
memb potential
3 postulates of the chemiosmotic theory
- the mito ETC translocates protons across the inner memb as e- flows from one e- carrier to the next
- ATP synthase uses the pmf to drive the phosphorylation of ADP
- inner mito memb is impermeable to H+ or OH- ions. if the memb is disrupted, pmf cannot be created and ATP cannot be made
structure of ATP synthase
= complex V embedded in inner memb F0 = embedded in memb F1 = protrudes into matrix side, contains the catalytic domains (subunits)
F1 subunits
a3, b3, y, d, e
- -a and b arranged alternately in hexagon
- -above a/b is a y/e stalk
- -both bind nucleotides, b is catalytically active
ATP synthase properties
- -form homodimers
- -dimers join to form oligomers
- -maintains curves of inner memb
- -cristae allow the proton gradient to be in close proximity to the ATP synthase
synthesis of ATP
- -catalyzed by a large memb bound protein
- -harness the nrg contained in pmf, ATP synthase obtains necessary power to form ATP = 7.3 kcal/mol
oligomycin
an inhibitor of ATP synthesis
disrupts proton transport thru the channel
mechanism of action of ATP-ADP translocase
–they are not permeable across mito memb, thus need a carrier
–ATP-ADP translocase family
…….are in outer/inner mito membs
–flow of ATP and ADP is coupled, ADP only enters matrix if ATP leaves (also complex VI)
reduced NADH cannot cross the ?
mito memb
so uses 2 shuttle systems
1. malate-aspartate shuttle
2. glycerophosphate shuttle
malate-aspartate shuttle
operates in heart, liver, kidneys
generates NADH in mito-matrix
NADH enters to ETC at complex I
glycerophosphate shuttle
operates in skeletal muscle, brain
generates FADH2 in the inner mito memb
FADH2 joins to ETC at CoQ
regulation of cellular respiration
- -levels of ATP regulate respiration
- -e- can only flow thru ETC when ADP is phosphorylated
regulation by ADP levels called respiratory control or acceptor control
inhibition of OxPhos
when transfer of e-‘s is inhibited
- -a decrease in the pumping protons
- -a decrease in the protein gradient
- -inhibition of ATP synthesis
uncoupling and heat generation – hibernating animals
some organisms can uncouple oxphos from ATP synthesis used to generate heat and maintain body temp
–happens in brown adipose tissue
uncoupling protein
inner mito memb contains uncoupling protein = thermogenin (UCP 1)
transfers protons from cytoplasm to matrix side
–nrg converted to heat
UCP 2 and UCP 3 also uncouple oxphos from ATP synthesis – playing a role in nrg homeostasis