Title: ATP SYNTHASE Bovine F1ATPase
1ATP SYNTHASE(Bovine F1-ATPase )
- By Ashley, David, and Angela
2ATP Synthase
- Enzyme
- Synthesizes ATP from ADP and inorganic phosphate
- Synthesizes various forms of energy
- Projects inward from inner mitochondrial
membranes. - Inhibited by the Dccd (Dicyclohexylcarbodiimide)
3Overview of Structure
- FoF1 particle resembles a mushroom
- Head is the F1 particle
- Stalk is gamma subunit of F1
- Base and roots are the Fo particle embedded in
the membrane - Antibiotic oligomycin inhibits the Fo unit
4Mechanism
Intermembrane space
H ions
- Occurs in the outer mitochondrion compartment,
only when NADH is made from oxidation reactions,
which generates a proton gradient. - As the protons build up, a proton gradient is
formed. - Protons (H) enter the cell through the ATP
synthase complex- a proton channel that allows
re-entry of protons - The upper part of the ATP synthase complex
rotates when a new H enters - ATP is synthesized by the resulting current of
protons flowing through the membrane.
Matrix
5Organisms
- Plants
- Chloroplast thylakoid membrane
- Bacteria
- Eubacteria
- Yeast
- Animal
- Humans
6Location within organism
- In plants
- ATP synthase occurs in the chloroplast and is
intergrated into the thylakoid membrane - F1 sticks in the stroma, where dark reaction of
photosynthesis and ATP synthesis take place. - In E. coli
- Simplest known form, with 8 different subunit
types - In yeast
- Most complex form, with 20 different subunit
types
7Disease caused by ATP Synthase
- Autosomal dominant polycystic kidney disease
(ADPKD) - Monogenic disease- a modified single gene
- The C. elegans polycystins LOV-1 and PKD-2 are
required for male mating behaviors and are
localized to sensory cilia. - ATP-2 and other ATP synthase components
colocalize with LOV-1 and PKD-2 in cilia. - Disrupts the function of the ATP synthase or over
expression of atp-2, which results in a male
mating behavior defect.
8Significance of ATP synthase
- The synthesis of ATP from ATP synthase causes a
concentration gradient. - Concentration gradients are key components to the
biological world. - The potential energy from these gradients are
often used to perform biological work.
9Application uses
- Bioremediation and biodegradation-uses
microorganisms to clean up contaminated
environments. - Oil spills
- Pollutants
- If it werent for ATP synthase, ATP would not be
stored in living - systems like
- microorganisms
10Crystal Structure of ATP SYNTHASE
11General features
- There are a total of 9 chains and they are all
amino acids - Chain A,B, C are all identical
- each has a total of 510 residues with gaps, 492
residues w/o gap. - (gap residues1 to18)
- Chain D
- has a total of 475 residues with gaps, 466
residues w/o gap. - (gap11 to 8 and gap2 200)
- Chain E and F are identical
- has a total of 474 residues with gaps, 466
residues w/o gap. - (gap residues 1 to 8)
- Chain G
- has total of 272 residues with gaps, 263 residue
w/o gaps. - (gap 1 62 to 66 and gap2 97 to 100)
- Chain H
- Has total of 145 residue with gaps, 131 w/o gaps
- (gap residues 1 to 14)
- Chain I
- Has total of 47 residue with gaps, no gaps
12CHOFAS
- Predicted number of helices 14
13GOR4
- Predicted number of helices 14
14PELE
- Predicted number of helices 14
15CHOFAS
16GOR4
17PELE
18Protein Explorer
- Total number of helices (red)145
- Total number of strands (yellow)107
19Ligands
- There are a total of 13 ligands for all 9 chains,
but Chain A has 2 ligands.
20Whats around Magnesium?
21Active sites
- Chain A was not crystallized with any inhibitors,
but general inhibitors for the enyzme,
Dicyclohexylcarbodiimide (DCCd) and Oligomycin. - Chain A LYS175A, ARG373A, ARG171A, GLN172A,
THR173A, GLY174A, LYS175A, THR176A, SER177A,
GLU328A, PHE357A, GLN430A, and GLN432A
22Domains
- There are 2 functional, which are F0 and F1.
- F1 ATPase
- Its the central domain.
- Found in bacterial plasma membranes,
mitochondrial inner membranes, and chloroplast
thylakoid membranes. - F1, is composed of alpha, beta, gamma, delta and
epsilon subunits(3a, 3ß, ?, d, e).
23Domain F0
- F0 Domain
- Is an integral membrane
- This portion is composed of 3 subunits
- A, 2-B, and 12-C
- 12-C subuints
- They are hydrophobic
- Arranged in two circle
- Circle one the inner circle, which consist of
amino terminal - Circle two the outer circle, which consist of
carboxyl terminal
24Structural Motif
- There is 1 interesting structural motifs found
for Chain A - PS00017 151-gt159 ATP_GTP_A PDOC00017
- The best conserved of these motifs is a
glycine-rich region, which typically forms a
flexible loop between a beta-strand and an
alpha-helix. This sequence motif is generally
referred to as the P-loop.
25Chain G Motif
- A dimerization motif GXXXG within the F0 domain
of the membrane-spanning segment - Alteration of this motif leads to the loss of
subunit g and of supramolecular structures of the
ATP synthase. - most highly studied mode of helix-helix
association - is known to act as a universal scaffold for the
assembly of two transmembrane helices
26 Multiple Sequence Alignment
27MSA Information
- Legend shows the conserved and non-conserved
regions of sequence. - Gaps are noted by a dash mark within the
sequence.
- There are no noted indels in the sequence.
28BOXSHADE Color-Coded Plots of Pre-Aligned
Sequences
Conserved region Identical region Similar region
29Comparisons
- Shows that there are 62.8 identical regions
between the sequences with many similar residues
scattered throughout. - Only 0.03 is considered a truly conserved region
among the five sequences
30Infer an Unrooted Phylogeny from PS Alignment
PROTPARS
100
100
(((Bacterium,Plant_Thaliana),(Purple_Sea_Urchin,1E
79_g_chain)),Asian_Rooster)
Draw Unrooted Phylogenetic Tree from Alignment
DRAWTREE
(((Asian_Rooster,1E79_G_Chain) 100,
Purple_Sea_Urchin) 100 Plant_Thaliana,Bacterium)
31Summary
- 9 chains
- 2 inhibitors
- Mushroom shaped with membrane and matrix regions
- Found in almost every organism on the earth
- Very important due synthesis of energy within the
organisms - Most closely related to the Asian rooster based
on our phylogenic trees
32Questions and Comments
33References
- http//www.who.int/genomics/public/geneticdiseases
/en/index2.html - http//www.wisc.edu/molpharm/faculty/barr/Pub15563
610.pdf - http//vcell.ndsu.nodak.edu/animations/atpgradient
/movie.htm - http//www.rpi.edu/dept/bcbp/molbiochem/MBWeb/mb1/
part2/f1fo.htm - http//en.wikipedia.org/wiki/ImageDCC_Structure.p
ng - http//www.mrc-dunn.cam.ac.uk/research/atp_synthas
e/ - http//www.nature.com/nsmb/journal/v7/n11/full/nsb
1100_1055.html - http//www.sp.uconn.edu/terry/images/anim/ATPmito
.html - http//www.life.uiuc.edu/crofts/bioph354/lect10.ht
ml - http//en.wikipedia.org/wiki/ATP_synthase
- http//nobelprize.org/nobel_prizes/chemistry/laure
ates/1997/press.html - http//nobelprize.org/nobel_prizes/chemistry/laure
ates/1997/press.html - http//www.ncbi.nlm.nih.gov/
- http//en.wikipedia.org/wiki/Bioremediation
- Diego M. Bustos J. Biol. Chem., Vol. 280, Issue
32, 29004-29010, August 12, 2005.
http//www.jbc.org/cgi/content/abstract/280/32/290
04 - Clyde Gibbons, Martin G. Montgomery, Andrew G. W.
Leslie John E. Walker. The structure of the
central stalk in bovine F1-ATPase at 2.4 Å
resolution. Nature Structural Biology 7, 1055 -
1061 (2000). 17 April, 2008