Literature DB >> 3736672

Post-translational insertion of a fragment of the glucose transporter into microsomes requires phosphoanhydride bond cleavage.

M Mueckler, H F Lodish.   

Abstract

Most eukaryotic secretory and membrane proteins insert co-translationally into the membrane of the rough endoplasmic reticulum (RER), and are targeted there by one or more NH2-terminal or internal signal sequences. However, little is known about the actual translocation and membrane integration processes. In particular, any energy requirements for targeting and integration have remained obscure because of the inability to uncouple the processes from concomitant protein synthesis. We recently showed that the human glucose transporter (GT), an integral membrane glycoprotein, can insert post-translationally into dog pancreatic microsomes with low but demonstrable efficiency in vitro, and that a fragment corresponding to the NH2-terminal 340 amino acids and 8 of the 12 membrane-spanning alpha-helixes of GT (GT-N) can insert with significantly greater efficiency. We report here that post-translational insertion of GT-N into pancreatic microsomes requires energy in the form of a phosphodiester bond, and suggest that co-translational insertion of proteins into the RER may also require energy independent of that used for polypeptide synthesis.

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Year:  1986        PMID: 3736672     DOI: 10.1038/322549a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  23 in total

1.  Determinant of the extracellular location of the N-terminus of human multidrug-resistance-associated protein.

Authors:  J T Zhang
Journal:  Biochem J       Date:  2000-06-15       Impact factor: 3.857

2.  The adenovirus E3-6.7K protein adopts diverse membrane topologies following posttranslational translocation.

Authors:  Alexander R Moise; Jason R Grant; Roger Lippé; Reinhard Gabathuler; Wilfred A Jefferies
Journal:  J Virol       Date:  2004-01       Impact factor: 5.103

3.  An ATP-binding membrane protein is required for protein translocation across the endoplasmic reticulum membrane.

Authors:  D L Zimmerman; P Walter
Journal:  Cell Regul       Date:  1991-10

4.  Membrane integration of in vitro-translated gap junctional proteins: co- and post-translational mechanisms.

Authors:  J T Zhang; M Chen; C I Foote; B J Nicholson
Journal:  Mol Biol Cell       Date:  1996-03       Impact factor: 4.138

5.  Predicting the orientation of eukaryotic membrane-spanning proteins.

Authors:  E Hartmann; T A Rapoport; H F Lodish
Journal:  Proc Natl Acad Sci U S A       Date:  1989-08       Impact factor: 11.205

6.  On the transfer of integral proteins into membranes.

Authors:  S J Singer; P A Maher; M P Yaffe
Journal:  Proc Natl Acad Sci U S A       Date:  1987-04       Impact factor: 11.205

Review 7.  The role of topogenic sequences in the movement of proteins through membranes.

Authors:  A Robinson; B Austen
Journal:  Biochem J       Date:  1987-09-01       Impact factor: 3.857

Review 8.  Biogenesis of mitochondrial porin: the import pathway.

Authors:  R Pfaller; R Kleene; W Neupert
Journal:  Experientia       Date:  1990-02-15

9.  Post-translational integration and oligomerization of connexin 26 in plasma membranes and evidence of formation of membrane pores: implications for the assembly of gap junctions.

Authors:  Shoeb Ahmad; W Howard Evans
Journal:  Biochem J       Date:  2002-08-01       Impact factor: 3.857

10.  An ATP- and hsc70-dependent oligomerization of nascent heat-shock factor (HSF) polypeptide suggests that HSF itself could be a "sensor" for the cellular stress response.

Authors:  M J Schlesinger; C Ryan
Journal:  Protein Sci       Date:  1993-08       Impact factor: 6.725

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