Literature DB >> 3525558

Structural requirement at the cleavage site for efficient processing of the lipoprotein secretory precursor of Escherichia coli.

S Inouye, G Duffaud, M Inouye.   

Abstract

A phenotypically silent mutation in the signal peptide of the Escherichia coli outer membrane prolipoprotein was combined with other mutations in the mature lipoprotein structure. Under conditions where the individual mutations permit normal lipoprotein secretion, the prolipoprotein with both mutations was unable to be normally modified or processed. These results demonstrate that a given signal peptide is fully functional only if it is structurally compatible with the protein to be secreted. This structural compatibility between the signal peptide and the secretory protein is considered to be dependent on the secondary structure formed at or near the signal peptide cleavage site.

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Year:  1986        PMID: 3525558

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


  15 in total

Review 1.  Export and sorting of the Escherichia coli outer membrane protein OmpA.

Authors:  R Freudl; M Klose; U Henning
Journal:  J Bioenerg Biomembr       Date:  1990-06       Impact factor: 2.945

2.  Enhancement of protein translocation across the membrane by specific mutations in the hydrophobic region of the signal peptide.

Authors:  J Goldstein; S Lehnhardt; M Inouye
Journal:  J Bacteriol       Date:  1990-03       Impact factor: 3.490

3.  Evidence for the loop model of signal-sequence insertion into the endoplasmic reticulum.

Authors:  A S Shaw; P J Rottier; J K Rose
Journal:  Proc Natl Acad Sci U S A       Date:  1988-10       Impact factor: 11.205

4.  Optimization of bacteriocin release protein (BRP)-mediated protein release by Escherichia coli: random mutagenesis of the pCloDF13-derived BRP gene to uncouple lethality and quasi-lysis from protein release.

Authors:  F J van der Wal; G Koningstein; C M ten Hagen; B Oudega; J Luirink
Journal:  Appl Environ Microbiol       Date:  1998-02       Impact factor: 4.792

5.  cDNA and genomic cloning and expression of the P48 monocytic differentiation/activation factor, a Mycoplasma fermentans gene product.

Authors:  R E Hall; S Agarwal; D P Kestler; J A Cobb; K M Goldstein; N S Chang
Journal:  Biochem J       Date:  1996-11-01       Impact factor: 3.857

6.  Positive charges at the NH2 terminus convert the membrane-anchor signal peptide of cytochrome P-450 to a secretory signal peptide.

Authors:  E Szczesna-Skorupa; N Browne; D Mead; B Kemper
Journal:  Proc Natl Acad Sci U S A       Date:  1988-02       Impact factor: 11.205

Review 7.  Lipoproteins in bacteria.

Authors:  S Hayashi; H C Wu
Journal:  J Bioenerg Biomembr       Date:  1990-06       Impact factor: 2.945

8.  In vivo analysis of sequence requirements for processing and degradation of the colicin A lysis protein signal peptide.

Authors:  S P Howard; L Lindsay
Journal:  J Bacteriol       Date:  1998-06       Impact factor: 3.490

9.  Molecular cloning, expression, and DNA sequence analysis of the gene that encodes the 16-kilodalton outer membrane lipoprotein of Serpulina hyodysenteriae.

Authors:  W Thomas; R Sellwood
Journal:  Infect Immun       Date:  1993-03       Impact factor: 3.441

10.  Molecular characterization of a conserved 20-kilodalton membrane-associated lipoprotein antigen of Helicobacter pylori.

Authors:  M Kostrzynska; P W O'Toole; D E Taylor; T J Trust
Journal:  J Bacteriol       Date:  1994-10       Impact factor: 3.490

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