Literature DB >> 2991529

Functional reconstitution of lens gap junction proteins into proteoliposomes.

H Nikaido, E Y Rosenberg.   

Abstract

Membranes rich in junction complexes were prepared from bovine lens, and the fragments of the membranes were reconstituted into proteoliposomes with a large excess of phosphatidylcholine and dicetylphosphate. The osmotic swelling behavior of these liposomes showed that the lens junction membranes contributed protein components that produced channels with a nominal diameter of 1.4 nm. Most preparations of lens junctions produced rates of osmotic swelling much slower than those found in proteoliposomes containing equivalent amounts of Escherichia coli porin, and we discuss several possible explanations for this observation.

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Year:  1985        PMID: 2991529     DOI: 10.1007/bf01872008

Source DB:  PubMed          Journal:  J Membr Biol        ISSN: 0022-2631            Impact factor:   1.843


  31 in total

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Journal:  Invest Ophthalmol       Date:  1965-08

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Authors:  E M RENKIN
Journal:  J Gen Physiol       Date:  1954-11-20       Impact factor: 4.086

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Authors:  D A Goodenough
Journal:  Invest Ophthalmol Vis Sci       Date:  1979-11       Impact factor: 4.799

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Authors:  W R Loewenstein
Journal:  Physiol Rev       Date:  1981-10       Impact factor: 37.312

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Authors:  G Schwarzmann; H Wiegandt; B Rose; A Zimmerman; D Ben-Haim; W R Loewenstein
Journal:  Science       Date:  1981-07-31       Impact factor: 47.728

6.  Bulk isolation of mouse hepatocyte gap junctions. Characterization of the principal protein, connexin.

Authors:  D A Goodenough
Journal:  J Cell Biol       Date:  1974-05       Impact factor: 10.539

7.  Calcium-mediated changes in gap junction structure: evidence from the low angle X-ray pattern.

Authors:  P N Unwin; P D Ennis
Journal:  J Cell Biol       Date:  1983-11       Impact factor: 10.539

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Authors:  C Peracchia; L L Peracchia
Journal:  J Cell Biol       Date:  1980-12       Impact factor: 10.539

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Authors:  E L Hertzberg; D J Anderson; M Friedlander; N B Gilula
Journal:  J Cell Biol       Date:  1982-01       Impact factor: 10.539

10.  Immunocytochemical localization of the main intrinsic polypeptide (MIP) in ultrathin frozen sections of rat lens.

Authors:  P G Fitzgerald; D Bok; J Horwitz
Journal:  J Cell Biol       Date:  1983-11       Impact factor: 10.539

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  7 in total

1.  Phosphorylation modulates the voltage dependence of channels reconstituted from the major intrinsic protein of lens fiber membranes.

Authors:  G R Ehring; N Lagos; G A Zampighi; J E Hall
Journal:  J Membr Biol       Date:  1992-02       Impact factor: 1.843

2.  Channel reconstitution in liposomes and planar bilayers with HPLC-purified MIP26 of bovine lens.

Authors:  L Shen; P Shrager; S J Girsch; P J Donaldson; C Peracchia
Journal:  J Membr Biol       Date:  1991-10       Impact factor: 1.843

3.  Reconstitution of channels from preparations enriched in lens gap junction protein MP70.

Authors:  P Donaldson; J Kistler
Journal:  J Membr Biol       Date:  1992-08       Impact factor: 1.843

4.  The permeability of reconstituted liposomes containing the purified lens fiber cell integral membrane proteins MP20, MP26 and MP70.

Authors:  L J Jarvis; C F Louis
Journal:  J Membr Biol       Date:  1992-12       Impact factor: 1.843

5.  Properties of channels reconstituted from the major intrinsic protein of lens fiber membranes.

Authors:  G R Ehring; G Zampighi; J Horwitz; D Bok; J E Hall
Journal:  J Gen Physiol       Date:  1990-09       Impact factor: 4.086

6.  The structural organization and protein composition of lens fiber junctions.

Authors:  G A Zampighi; J E Hall; G R Ehring; S A Simon
Journal:  J Cell Biol       Date:  1989-06       Impact factor: 10.539

7.  Electron microscopic observations of reconstituted proteoliposomes with the purified major intrinsic membrane protein of eye lens fibers.

Authors:  I Dunia; S Manenti; A Rousselet; E L Benedetti
Journal:  J Cell Biol       Date:  1987-10       Impact factor: 10.539

  7 in total

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