Literature DB >> 3720742

Structure of initiation factor eIF-3 from rat liver. Hydrodynamic and electron microscopic investigations.

J Behlke, U A Bommer, G Lutsch, A Henske, H Bielka.   

Abstract

On the basis of hydrodynamic, electron microscopic and biochemical investigations a new model of the structure of initiation factor eIF-3 is proposed. From sedimentation and diffusion coefficients of 16.35 S and 2.13 X 10(-7) cm2/s, respectively, as well as from sedimentation equilibrium measurements, a molecular mass of about 650 kDa was determined for isolated eIF-3. This is in agreement with molecular mass estimations by sodium dodecyl sulphate gel electrophoresis. A partial specific volume of 0.723 cm3/g was determined by means of the amino acid composition and the specific volume increments of the amino acids. From this value and from the molecular mass, a volume of 780 nm3 was calculated for eIF-3. In electron micrographs of isolated eIF-3, images with triangular profiles and side lengths of 14 nm, 16 nm, and 17 nm have been observed. Taking into account the calculated volume and considering the triangular image as one face of the particle, it is suggested that eIF-3 has the shape of a flat triangular prism with a height of about 7 nm and the above-mentioned side-lengths. This model is in agreement with results of electron microscopic investigations of eIF-3 in native small ribosomal subunits [Lutsch, G., Benndorf, R., Westermann, P., Bommer, U.-A. & Bielka, H. (1986) Eur. J. Cell Biol. 40/2, in press]. The high frictional ratio of about 1.7 also supports eIF-3 to be rather of a flat than of a globular shape.

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Year:  1986        PMID: 3720742     DOI: 10.1111/j.1432-1033.1986.tb09698.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  7 in total

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Authors:  Amsaveni Ramachandran; Sriram Ravindran; Anne George
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2.  VIP21-caveolin, a membrane protein constituent of the caveolar coat, oligomerizes in vivo and in vitro.

Authors:  S Monier; R G Parton; F Vogel; J Behlke; A Henske; T V Kurzchalia
Journal:  Mol Biol Cell       Date:  1995-07       Impact factor: 4.138

3.  Molecular mass determination by sedimentation velocity experiments and direct fitting of the concentration profiles.

Authors:  J Behlke; O Ristau
Journal:  Biophys J       Date:  1997-01       Impact factor: 4.033

4.  A region rich in aspartic acid, arginine, tyrosine, and glycine (DRYG) mediates eukaryotic initiation factor 4B (eIF4B) self-association and interaction with eIF3.

Authors:  N Méthot; M S Song; N Sonenberg
Journal:  Mol Cell Biol       Date:  1996-10       Impact factor: 4.272

5.  Reconstitution reveals the functional core of mammalian eIF3.

Authors:  Mamiko Masutani; Nahum Sonenberg; Shigeyuki Yokoyama; Hiroaki Imataka
Journal:  EMBO J       Date:  2007-06-21       Impact factor: 11.598

6.  Identification of a translation initiation factor 3 (eIF3) core complex, conserved in yeast and mammals, that interacts with eIF5.

Authors:  L Phan; X Zhang; K Asano; J Anderson; H P Vornlocher; J R Greenberg; J Qin; A G Hinnebusch
Journal:  Mol Cell Biol       Date:  1998-08       Impact factor: 4.272

Review 7.  Human eIF3: from 'blobology' to biological insight.

Authors:  Jamie H D Cate
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2017-03-19       Impact factor: 6.237

  7 in total

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