ArticleProceedings of the National Academy of Sciences of the United States of America1998
Membrane-bound state of the colicin E1 channel domain as an extended two-dimensional helical array.
Article in Proceedings of the National Academy of Sciences of the United States of America, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.
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17 citing papers in PubMed.
- Spectroscopic evidence of tetanus toxin translocation domain bilayer-induced refolding and insertion.Biophysical journal · 2021Article
- The Cytoplasm-Entry Domain of Antibacterial CdiA Is a Dynamic α-Helical Bundle with Disulfide-Dependent Structural Features.Journal of molecular biology · 2019Article
- Membrane partitioning of the pore-forming domain of colicin A. Role of the hydrophobic helical hairpin.Biophysical journal · 2013Article
- Quantification of transition dipole strengths using 1D and 2D spectroscopy for the identification of molecular structures via exciton delocalization: application to α-helices.The Journal of chemical physics · 2012Article
- Hydrophilic residues are crucial for ribosomal protein L11 (RPL11) interaction with zinc finger domain of MDM2 and p53 protein activation.The Journal of biological chemistry · 2011Article
- Article
- Low pH-induced pore formation by the T domain of botulinum toxin type A is dependent upon NaCl concentration.The Journal of membrane biology · 2010Article
- pH (low) insertion peptide (pHLIP) inserts across a lipid bilayer as a helix and exits by a different path.Proceedings of the National Academy of Sciences of the United States of America · 2010Article
- Colicin biology.Microbiology and molecular biology reviews : MMBR · 2007Review
- Interactions of apomyoglobin with membranes: mechanisms and effects on heme uptake.Protein science : a publication of the Protein Society · 2007Article
- Chemical and photochemical modification of colicin E1 and gramicidin A in bilayer lipid membranes.The Journal of membrane biology · 2004Article
- Evidence for crucial electrostatic interactions between Bcl-2 homology domains BH3 and BH4 in the anti-apoptotic Nr-13 protein.The Biochemical journal · 2002Article
- Tuning the membrane surface potential for efficient toxin import.Proceedings of the National Academy of Sciences of the United States of America · 2002Article
- Identification of specific residues in colicin E1 involved in immunity protein recognition.Journal of bacteriology · 2001Article
- Optical anisotropy in lipid bilayer membranes: coupled plasmon-waveguide resonance measurements of molecular orientation, polarizability, and shape.Biophysical journal · 2001Article
- Unfolding and refolding of cytochrome c driven by the interaction with lipid micelles.Protein science : a publication of the Protein Society · 2000Article
- Structure in the channel forming domain of colicin E1 bound to membranes: the 402-424 sequence.Protein science : a publication of the Protein Society · 1999Article
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7 authors.
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Abstract
Atomic level structures have been determined for the soluble forms of several colicins and toxins, but the structural changes that occur after membrane binding have not been well characterized. Changes occurring in the transition from the soluble to membrane-bound state of the C-terminal 190-residue channel polypeptide of colicin E1 (P190) bound to anionic membranes are described. In the membrane-bound state, the alpha-helical content increases from 60-64% to 80-90%, with a concomitant increase in the average length of the helical segments from 12 to 16 or 17 residues, close to the length required to span the membrane bilayer in the open channel state. The average distance between helical segments is increased and interhelix interactions are weakened, as shown by a major loss of tertiary structure interactions, decreased efficiency of fluorescence resonance energy transfer from an energy donor on helix V of P190 to an acceptor on helix IX, and decreased resonance energy transfer at higher temperatures, not observed in soluble P190, implying freedom of motion of helical segments. Weaker interactions are also shown by a calorimetric thermal transition of low cooperativity, and the extended nature of the helical array is shown by a 3- to 4-fold increase in the average area subtended per molecule to 4,200 A2 on the membrane surface. The latter, with analysis of the heat capacity changes, implies the absence of a developed hydrophobic core in the membrane-bound P190. The membrane interfacial layer thus serves to promote formation of a highly helical extended two-dimensional flexible net. The properties of the membrane-bound state of the colicin channel domain (i.e., hydrophobic anchor, lengthened and loosely coupled alpha-helices, and close association with the membrane interfacial layer) are plausible structural features for the state that is a prerequisite for voltage gating, formation of transmembrane helices, and channel opening.
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