Literature DB >> 2457024

An amino acid sequence which directs membrane insertion causes loss of membrane potential.

J I Horabin1, R E Webster.   

Abstract

A 55-amino acid segment, normally present between residues 241 and 295 of the 348-residue gene I protein of the filamentous bacteriophage f1, acts as an internal signal sequence for gene I protein or, when present in fusion proteins, for EcoRI endonuclease or alkaline phosphatase. The resulting proteins are inserted so that they span the membrane with sequences on the amino side of the 55-residue segment in the cytoplasm and those near the carboxy side outside the cytoplasmic membrane. The presence of these proteins in the membrane results in the rapid inhibition of cell growth, probably from a loss of the membrane potential. We describe some of the elements in this 55-residue segment that appear to be crucial for its interaction with the membrane.

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Year:  1988        PMID: 2457024

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


  10 in total

1.  Membrane localization and topology of a viral assembly protein.

Authors:  J K Guy-Caffey; M P Rapoza; K A Jolley; R E Webster
Journal:  J Bacteriol       Date:  1992-04       Impact factor: 3.490

Review 2.  Alkaline phosphatase fusions: sensors of subcellular location.

Authors:  C Manoil; J J Mekalanos; J Beckwith
Journal:  J Bacteriol       Date:  1990-02       Impact factor: 3.490

3.  A mutation in the amino terminus of a hybrid TrpC-TonB protein relieves overproduction lethality and results in cytoplasmic accumulation.

Authors:  J T Skare; S K Roof; K Postle
Journal:  J Bacteriol       Date:  1989-08       Impact factor: 3.490

Review 4.  Insertion of proteins into bacterial membranes: mechanism, characteristics, and comparisons with the eucaryotic process.

Authors:  M H Saier; P K Werner; M Müller
Journal:  Microbiol Rev       Date:  1989-09

5.  Gene A32 product of vaccinia virus may be an ATPase involved in viral DNA packaging as indicated by sequence comparisons with other putative viral ATPases.

Authors:  E V Koonin; T G Senkevich; V I Chernos
Journal:  Virus Genes       Date:  1993-02       Impact factor: 2.332

6.  The filamentous bacteriophage assembly proteins require the bacterial SecA protein for correct localization to the membrane.

Authors:  M P Rapoza; R E Webster
Journal:  J Bacteriol       Date:  1993-03       Impact factor: 3.490

7.  Analysis of the structure and subcellular location of filamentous phage pIV.

Authors:  M Russel; B Kaźmierczak
Journal:  J Bacteriol       Date:  1993-07       Impact factor: 3.490

8.  Genetic analysis of the filamentous bacteriophage packaging signal and of the proteins that interact with it.

Authors:  M Russel; P Model
Journal:  J Virol       Date:  1989-08       Impact factor: 5.103

9.  Expression of chimeric ras protein with OmpF signal peptide in Escherichia coli: localization of OmpF fusion protein in the inner membrane.

Authors:  T Yamamoto; N Okawa; T Endo; A Kaji
Journal:  Appl Microbiol Biotechnol       Date:  1991-08       Impact factor: 4.813

10.  Specific localization of the lysis protein of bacteriophage MS2 in membrane adhesion sites of Escherichia coli.

Authors:  B Walderich; J V Höltje
Journal:  J Bacteriol       Date:  1989-06       Impact factor: 3.490

  10 in total

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