Literature DB >> 6309789

Comparison of the macroscopic and single channel conductance properties of colicin E1 and its COOH-terminal tryptic peptide.

J O Bullock, F S Cohen, J R Dankert, W A Cramer.   

Abstract

A COOH-terminal tryptic fragment (Mr approximately equal to 20,000) of colicin E1 has been proposed to contain the membrane channel-forming domain of the colicin molecule. A comparison is made of the conductance properties of colicin E1 and its COOH-terminal fragment in planar bilayer membranes. The macroscopic and single channel properties of colicin E1 and its COOH-terminal tryptic fragment are very similar, if not indistinguishable, implying that the NH2-terminal, two-thirds of the colicin E1 molecule, does not significantly influence its channel properties. The channel-forming activity of both polypeptides is dependent upon the presence of a membrane potential, negative on the trans side of the membrane. The average single channel conductance of colicin E1 and the COOH-terminal fragment is 20.9 +/- 3.9 and 19.1 +/- 2.9 picosiemens, respectively. The rate at which both proteins form conducting channels increases as the pH is lowered from 7 to 5. Both molecules require negatively charged lipids for activity to be expressed, exhibit the same ion selectivity, and rectify the current to the same extent. Both polypeptides associate irreversibly with the membrane in the absence of voltage, but subsequent formation of conducting channels requires a negative membrane potential.

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Year:  1983        PMID: 6309789

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


  28 in total

1.  Colicin E1 forms a dimer after urea-induced unfolding.

Authors:  B A Steer; A A DiNardo; A R Merrill
Journal:  Biochem J       Date:  1999-06-15       Impact factor: 3.857

2.  Tuning the membrane surface potential for efficient toxin import.

Authors:  Stanislav D Zakharov; Tatyana I Rokitskaya; Vladimir L Shapovalov; Yuri N Antonenko; William A Cramer
Journal:  Proc Natl Acad Sci U S A       Date:  2002-06-11       Impact factor: 11.205

3.  Constraints imposed by protease accessibility on the trans-membrane and surface topography of the colicin E1 ion channel.

Authors:  Y L Zhang; W A Cramer
Journal:  Protein Sci       Date:  1992-12       Impact factor: 6.725

4.  Ion selectivity of colicin E1: II. Permeability to organic cations.

Authors:  J O Bullock; E R Kolen; J L Shear
Journal:  J Membr Biol       Date:  1992-05       Impact factor: 1.843

5.  Characterization of a novel microcin that kills enterohemorrhagic Escherichia coli O157:H7 and O26.

Authors:  Lauren J Eberhart; James R Deringer; Kelly A Brayton; Ashish A Sawant; Thomas E Besser; Douglas R Call
Journal:  Appl Environ Microbiol       Date:  2012-07-06       Impact factor: 4.792

6.  Formation of ion channels by colicin B in planar lipid bilayers.

Authors:  J O Bullock; S K Armstrong; J L Shear; D P Lies; M A McIntosh
Journal:  J Membr Biol       Date:  1990-03       Impact factor: 1.843

7.  Colicin N forms voltage- and pH-dependent channels in planar lipid bilayer membranes.

Authors:  H U Wilmsen; A P Pugsley; F Pattus
Journal:  Eur Biophys J       Date:  1990       Impact factor: 1.733

8.  Membrane topography of ColE1 gene products: the hydrophobic anchor of the colicin E1 channel is a helical hairpin.

Authors:  H Y Song; F S Cohen; W A Cramer
Journal:  J Bacteriol       Date:  1991-05       Impact factor: 3.490

9.  Localization of the immunity protein-reactive domain in unmodified and chemically modified COOH-terminal peptides of colicin E1.

Authors:  L J Bishop; E S Bjes; V L Davidson; W A Cramer
Journal:  J Bacteriol       Date:  1985-10       Impact factor: 3.490

10.  Ion selectivity of colicin E1: III. Anion permeability.

Authors:  J O Bullock; E R Kolen
Journal:  J Membr Biol       Date:  1995-03       Impact factor: 1.843

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