Literature DB >> 1331039

H+ transport and coupling by the F0 sector of the ATP synthase: insights into the molecular mechanism of function.

R H Fillingame1.   

Abstract

The F0 sector of the ATP synthase complex facilitates proton translocation through the membrane, and via interaction with the F1 sector, couples proton transport to ATP synthesis. The molecular mechanism of function is being probed by a combination of mutant analysis and structural biochemistry, and recent progress on the Escherichia coli F0 sector is reviewed here. The E. coli F0 is composed of three types of subunits (a, b, and c) and current information on their folding and organization in F0 is reviewed. The structure of purified subunit c in chloroform-methanol-H2O resembles that in native F0, and progress in determining the structure by NMR methods is reviewed. Genetic experiments suggest that the two helices of subunit c must interact as a functional unit around an essential carboxyl group as protons are transported. In addition, a unique class of suppressor mutations identify a transmembrane helix of subunit a that is proposed to interact with the bihelical unit of subunit c during proton transport. The role of multiple units of subunit c in coupling proton translocation to ATP synthesis is considered. The special roles of Asp61 of subunit c and Arg210 of subunit a in proton translocation are also discussed.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1331039     DOI: 10.1007/bf00762366

Source DB:  PubMed          Journal:  J Bioenerg Biomembr        ISSN: 0145-479X            Impact factor:   2.945


  25 in total

1.  Deletions in hydrophilic domains of subunit a from the Escherichia coli F1F0-ATP synthase interfere with membrane insertion or F0 assembly.

Authors:  M J Lewis; R D Simoni
Journal:  J Biol Chem       Date:  1992-02-15       Impact factor: 5.157

2.  Mutations in three of the putative transmembrane helices of subunit a of the Escherichia coli F1F0-ATPase disrupt ATP-driven proton translocation.

Authors:  C R Paule; R H Fillingame
Journal:  Arch Biochem Biophys       Date:  1989-10       Impact factor: 4.013

3.  A topological analysis of subunit alpha from Escherichia coli F1F0-ATP synthase predicts eight transmembrane segments.

Authors:  M J Lewis; J A Chang; R D Simoni
Journal:  J Biol Chem       Date:  1990-06-25       Impact factor: 5.157

4.  The essential carboxyl group in subunit c of the F1F0 ATP synthase can be moved and H(+)-translocating function retained.

Authors:  M J Miller; M Oldenburg; R H Fillingame
Journal:  Proc Natl Acad Sci U S A       Date:  1990-07       Impact factor: 11.205

5.  Subunit interactions within the chloroplast ATP synthase (CF0-CF1) as deduced by specific depletion of CF0 polypeptides.

Authors:  Y Feng; R E McCarty
Journal:  J Biol Chem       Date:  1990-07-25       Impact factor: 5.157

6.  Cross-linking and labeling of the Escherichia coli F1F0-ATP synthase reveal a compact hydrophilic portion of F0 close to an F1 catalytic subunit.

Authors:  J P Aris; R D Simoni
Journal:  J Biol Chem       Date:  1983-12-10       Impact factor: 5.157

Review 7.  The mechanism and regulation of ATP synthesis by F1-ATPases.

Authors:  R L Cross
Journal:  Annu Rev Biochem       Date:  1981       Impact factor: 23.643

8.  Proton translocation by the F1F0ATPase of Escherichia coli. Mutagenic analysis of the a subunit.

Authors:  B D Cain; R D Simoni
Journal:  J Biol Chem       Date:  1989-02-25       Impact factor: 5.157

9.  Topology, organization, and function of the psi subunit in the F0 sector of the H+-ATPase of Escherichia coli.

Authors:  J Hermolin; J Gallant; R H Fillingame
Journal:  J Biol Chem       Date:  1983-12-10       Impact factor: 5.157

10.  H+-ATPase activity of Escherichia coli F1F0 is blocked after reaction of dicyclohexylcarbodiimide with a single proteolipid (subunit c) of the F0 complex.

Authors:  J Hermolin; R H Fillingame
Journal:  J Biol Chem       Date:  1989-03-05       Impact factor: 5.157

View more
  7 in total

1.  Protein-like proton exchange in a synthetic host cavity.

Authors:  William M Hart-Cooper; Carmelo Sgarlata; Charles L Perrin; F Dean Toste; Robert G Bergman; Kenneth N Raymond
Journal:  Proc Natl Acad Sci U S A       Date:  2015-11-30       Impact factor: 11.205

2.  Comparative biochemical studies of ATPases in cells from patients with the T8993G or T8993C mitochondrial DNA mutations.

Authors:  M E Vázquez-Memije; S Shanske; F M Santorelli; P Kranz-Eble; D C DeVivo; S DiMauro
Journal:  J Inherit Metab Dis       Date:  1998-12       Impact factor: 4.982

Review 3.  Vacuolar H(+)-ATPase: from mammals to yeast and back.

Authors:  N Nelson; D J Klionsky
Journal:  Experientia       Date:  1996-12-15

4.  Structure analysis of membrane-reconstituted subunit c-ring of E. coli H+-ATP synthase by solid-state NMR.

Authors:  Yasuto Todokoro; Masatoshi Kobayashi; Takeshi Sato; Toru Kawakami; Ikuko Yumen; Saburo Aimoto; Toshimichi Fujiwara; Hideo Akutsu
Journal:  J Biomol NMR       Date:  2010-07-02       Impact factor: 2.835

Review 5.  The mitochondrial ATP synthase of Trypanosoma brucei: structure and regulation.

Authors:  N Williams
Journal:  J Bioenerg Biomembr       Date:  1994-04       Impact factor: 2.945

6.  Cytoplasmic transfer of the mtDNA nt 8993 T-->G (ATP6) point mutation associated with Leigh syndrome into mtDNA-less cells demonstrates cosegregation with a decrease in state III respiration and ADP/O ratio.

Authors:  I Trounce; S Neill; D C Wallace
Journal:  Proc Natl Acad Sci U S A       Date:  1994-08-30       Impact factor: 11.205

Review 7.  Rotor subunits adaptations in ATP synthases from photosynthetic organisms.

Authors:  Anthony Cheuk; Thomas Meier
Journal:  Biochem Soc Trans       Date:  2021-04-30       Impact factor: 5.407

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.