Literature DB >> 2862141

Size of the plasma membrane H+-ATPase from Neurospora crassa determined by radiation inactivation and comparison with the sarcoplasmic reticulum Ca2+-ATPase from skeletal muscle.

B J Bowman, C J Berenski, C Y Jung.   

Abstract

Using radiation inactivation, we have measured the size of the H+-ATPase in Neurospora crassa plasma membranes. Membranes were exposed to either high energy electrons from a Van de Graaff generator or to gamma irradiation from 60Co. Both forms of radiation caused an exponential loss of ATPase activity in parallel with the physical destruction of the Mr = 104,000 polypeptide of which this enzyme is composed. By applying target theory, the size of the H+-ATPase in situ was found to be approximately 2.3 X 10(5) daltons. We also used radiation inactivation to measure the size of the Ca2+-ATPase of sarcoplasmic reticulum and got a value of approximately 2.4 X 10(5) daltons, in agreement with previous reports. By irradiating a mixture of Neurospora plasma membranes and rabbit sarcoplasmic reticulum, we directly compared the sizes of these two ATPases and found them to be essentially the same. We conclude that both H+-ATPase and Ca2+-ATPase are oligomeric enzymes, most likely composed of two approximately 100,000-dalton polypeptides.

Entities:  

Mesh:

Substances:

Year:  1985        PMID: 2862141

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  14 in total

1.  In vivo cross-linking supports a head-to-tail mechanism for regulation of the plant plasma membrane P-type H+-ATPase.

Authors:  Thao T Nguyen; Grzegorz Sabat; Michael R Sussman
Journal:  J Biol Chem       Date:  2018-09-14       Impact factor: 5.157

2.  Structural studies of the vacuolar membrane ATPase from Neurospora crassa and comparison with the tonoplast membrane ATPase from Zea mays.

Authors:  E J Bowman; S Mandala; L Taiz; B J Bowman
Journal:  Proc Natl Acad Sci U S A       Date:  1986-01       Impact factor: 11.205

3.  Effects of ionizing radiations on proteins. Evidence of non-random fragmentations and a caution in the use of the method for determination of molecular mass.

Authors:  M Le Maire; L Thauvette; B de Foresta; A Viel; G Beauregard; M Potier
Journal:  Biochem J       Date:  1990-04-15       Impact factor: 3.857

4.  Radiation-damaged tyrosinase molecules are inactive.

Authors:  E S Kempner; J H Miller
Journal:  Biophys J       Date:  1989-01       Impact factor: 4.033

5.  Pleiotropic plasma membrane ATPase mutations of Saccharomyces cerevisiae.

Authors:  J H McCusker; D S Perlin; J E Haber
Journal:  Mol Cell Biol       Date:  1987-11       Impact factor: 4.272

Review 6.  H+-ATPases from mitochondria, plasma membranes, and vacuoles of fungal cells.

Authors:  B J Bowman; E J Bowman
Journal:  J Membr Biol       Date:  1986       Impact factor: 1.843

7.  Effects of solubilization on the inhibition of the p-type ATPase from maize roots by N-(ethoxycarbonyl)-2-ethoxy-1,2-dihydroquinoline.

Authors:  D K Brauer; M Gurriel; S I Tu
Journal:  Plant Physiol       Date:  1992-12       Impact factor: 8.340

Review 8.  Genetic and cell biological aspects of the yeast vacuolar H(+)-ATPase.

Authors:  Y Anraku; N Umemoto; R Hirata; Y Ohya
Journal:  J Bioenerg Biomembr       Date:  1992-08       Impact factor: 2.945

9.  Inactivation of secretory phospholipase A2 by ionizing radiation.

Authors:  L J Reynolds; E S Kempner; L L Hughes; E A Dennis
Journal:  Biophys J       Date:  1995-05       Impact factor: 4.033

Review 10.  Chemiosmotic coupling of ion transport in the yeast vacuole: its role in acidification inside organelles.

Authors:  Y Wada; Y Anraku
Journal:  J Bioenerg Biomembr       Date:  1994-12       Impact factor: 2.945

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.