Evidence map›Paper›PMID 15452437›Full record

ArticleJournal of biomolecular NMR2004

Characterisation of a mobile protein-binding epitope in the translocation domain of colicin E9.

Colin J Macdonald, Kaeko Tozawa, Emily S Collins, Christopher N Penfold, Richard James, Colin Kleanthous, Nigel J Clayden, Geoffrey R Moore

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Article in Journal of biomolecular NMR, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

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0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Colicin biology.Microbiology and molecular biology reviews : MMBR · 2007
    Review
  5. Competitive recruitment of the periplasmic translocation portal TolB by a natively disordered domain of colicin E9.Proceedings of the National Academy of Sciences of the United States of America · 2006
    Article
  6. Article
4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Colin J MacdonaldSchool of Chemical Sciences and Pharmacy, University of East Anglia, Norwich NR4 7TJ, UK.
Kaeko Tozawa
Emily S Collins
Christopher N Penfold
Richard James
Colin Kleanthous
Nigel J Clayden
Geoffrey R Moore

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The 61 kDa colicin E9 protein toxin enters the cytoplasm of susceptible cells by interacting with outer membrane and periplasmic helper proteins, and kills them by hydrolysing their DNA. The membrane translocation function is located in the N-terminal domain of the colicin, with a key signal sequence being a pentapeptide region that governs the interaction with the helper protein TolB (the TolB box). Previous NMR studies (Collins et al., 2002 J. Mol. Biol. 318, 787-804) have shown that the N-terminal 83 residues of colicin E9, which includes the TolB box, is largely unstructured and highly flexible. In order to further define the properties of this region we have studied a fusion protein containing residues 1-61 of colicin E9 connected to the N-terminus of the E9 DNase by an eight-residue linking sequence. 53 of the expected 58 backbone NH resonances for the first 61 residues and all of the expected 7 backbone NH resonances of the linking sequence were assigned with 3D (1)H-(13)C-(15)N NMR experiments, and the backbone dynamics of these regions investigated through measurement of (1)H-(15)N relaxation properties. Reduced spectral density mapping, extended Lipari-Szabo modelling, and fitting backbone R(2) relaxation rates to a polymer dynamics model identifies three clusters of interacting residues, each containing a tryptophan. Each of these clusters is perturbed by TolB binding to the intact colicin, showing that the significant region for TolB binding extends beyond the recognized five amino acids of the TolB box and demonstrating that the binding epitope for TolB involves a considerable degree of order within an otherwise disordered and flexible domain. Abbreviations : Im9, the immunity protein for colicin E9; E9 DNase, the endonuclease domain of colicin E9; HSQC, heteronuclear single quantum coherence; ppm, parts per million; DSS, 2,2-(dimethylsilyl)propanesulfonic acid; TSP, sodium 3-trimethylsilypropionate; T(1 - 61)-DNase fusion protein, residues 1-61 of colicin E9 connected to the N-terminus of the E9 DNase by an eight residue thrombin cleavage sequence.

Indexed as

Amino Acid SequenceBinding SitesBiological Transport, ActiveCarbon IsotopesColicinsDeoxyribonucleasesEpitopesEscherichia coliEscherichia coli ProteinsMolecular WeightNitrogen IsotopesNuclear Magnetic Resonance, BiomolecularProtein BindingProtein ConformationProtein Structure, TertiaryQuantum TheoryCarbon IsotopesColicinsDeoxyribonucleasesEpitopesEscherichia coli ProteinsNitrogen Isotopes

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.