Literature DB >> 7532020

Molecular flexibility demonstrated by paramagnetic enhancements of nuclear relaxation. Application to alamethicin: a voltage-gated peptide channel.

C L North1, J C Franklin, R G Bryant, D S Cafiso.   

Abstract

A nitroxide spin label attached to the C-terminus of the channel forming peptide alamethicin produces an enhancement of the nuclear spin-lattice relaxation rates of peptide protons as a result of both intermolecular and intramolecular magnetic dipole-dipole interactions. The intermolecular contribution provides evidence that alamethicin monomers collide preferentially in a C-terminal-to-N-terminal configuration in methanol. From the intramolecular paramagnetic enhancement of nuclear spin-lattice relaxation times, effective distances between the unpaired electron on the nitroxide at the C-terminus of alamethicin and protons along the peptide backbone were calculated. These distances are much shorter than distances based on the reported crystal structure of alamethicin, and cannot be accounted for by motion in the bonds that attach the nitroxide to the peptide. In addition, the differences between distances deduced from the nuclear spin relaxation and the distances seen in the crystal structure increase toward the N-terminal end of the peptide. The simplest explanation for these data is that the alamethicin backbone suffers large structural fluctuations that yield shorter effective distances between the C-terminus and positions along the backbone. This finding can be interpreted in terms of a molecular mechanism for the voltage-gating of the alamethicin channel. When the distances between a paramagnetic center and a nucleus fluctuate, paramagnetic enhancements are expected to yield distances that are weighted by r-6, and distances calculated using the Solomon-Bloembergen equations may more nearly represent a distance of closest approach than a time average distance. Therefore, the use of paramagnetic centers such as spin labels or metal ions with long electron T1 values provides a distance measurement that reflects a dynamically averaged structure where the averaging process heavily weights short distances. The results of such measurements, when combined with other structural information, may provide particularly clear evidence for the magnitude of structural fluctuations involving distances greater than 10 A.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 7532020      PMCID: PMC1225559          DOI: 10.1016/S0006-3495(94)80667-8

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  11 in total

1.  Internal motional averaging and three-dimensional structure determination by nuclear magnetic resonance.

Authors:  C B Post
Journal:  J Mol Biol       Date:  1992-04-20       Impact factor: 5.469

2.  Restrained and unrestrained molecular dynamics simulations in the NVT ensemble of alamethicin.

Authors:  F Fraternali
Journal:  Biopolymers       Date:  1990       Impact factor: 2.505

3.  Dynamics and aggregation of the peptide ion channel alamethicin. Measurements using spin-labeled peptides.

Authors:  S J Archer; J F Ellena; D S Cafiso
Journal:  Biophys J       Date:  1991-08       Impact factor: 4.033

Review 4.  Alamethicin: a peptide model for voltage gating and protein-membrane interactions.

Authors:  D S Cafiso
Journal:  Annu Rev Biophys Biomol Struct       Date:  1994

5.  A voltage-gated ion channel model inferred from the crystal structure of alamethicin at 1.5-A resolution.

Authors:  R O Fox; F M Richards
Journal:  Nature       Date:  1982-11-25       Impact factor: 49.962

6.  Uniform 15N labeling of a fungal peptide: the structure and dynamics of an alamethicin by 15N and 1H NMR spectroscopy.

Authors:  A A Yee; J D O'Neil
Journal:  Biochemistry       Date:  1992-03-31       Impact factor: 3.162

7.  Backbone dynamics of calmodulin studied by 15N relaxation using inverse detected two-dimensional NMR spectroscopy: the central helix is flexible.

Authors:  G Barbato; M Ikura; L E Kay; R W Pastor; A Bax
Journal:  Biochemistry       Date:  1992-06-16       Impact factor: 3.162

8.  Determination of the molecular dynamics of alamethicin using 13C NMR: implications for the mechanism of gating of a voltage-dependent channel.

Authors:  L P Kelsh; J F Ellena; D S Cafiso
Journal:  Biochemistry       Date:  1992-06-09       Impact factor: 3.162

Review 9.  Alamethicin and related membrane channel forming polypeptides.

Authors:  M K Mathew; P Balaram
Journal:  Mol Cell Biochem       Date:  1983       Impact factor: 3.396

10.  High-resolution 1H NMR study of the solution structure of alamethicin.

Authors:  G Esposito; J A Carver; J Boyd; I D Campbell
Journal:  Biochemistry       Date:  1987-02-24       Impact factor: 3.162

View more
  14 in total

1.  Site-directed parallel spin-labeling and paramagnetic relaxation enhancement in structure determination of membrane proteins by solution NMR spectroscopy.

Authors:  Binyong Liang; John H Bushweller; Lukas K Tamm
Journal:  J Am Chem Soc       Date:  2006-04-05       Impact factor: 15.419

2.  Helix bending in alamethicin: molecular dynamics simulations and amide hydrogen exchange in methanol.

Authors:  N Gibbs; R B Sessions; P B Williams; C E Dempsey
Journal:  Biophys J       Date:  1997-06       Impact factor: 4.033

3.  Simulation studies of alamethicin-bilayer interactions.

Authors:  P C Biggin; J Breed; H S Son; M S Sansom
Journal:  Biophys J       Date:  1997-02       Impact factor: 4.033

4.  Structure Changes of a Membrane Polypeptide under an Applied Voltage Observed with Surface-Enhanced 2D IR Spectroscopy.

Authors:  Erin R Birdsall; Megan K Petti; Vivek Saraswat; Joshua S Ostrander; Michael S Arnold; Martin T Zanni
Journal:  J Phys Chem Lett       Date:  2021-02-12       Impact factor: 6.475

5.  Distance estimates from paramagnetic enhancements of nuclear relaxation in linear and flexible model peptides.

Authors:  J Jacob; B Baker; R G Bryant; D S Cafiso
Journal:  Biophys J       Date:  1999-08       Impact factor: 4.033

6.  Hydrogen bonding in helical polypeptides from molecular dynamics simulations and amide hydrogen exchange analysis: alamethicin and melittin in methanol.

Authors:  R B Sessions; N Gibbs; C E Dempsey
Journal:  Biophys J       Date:  1998-01       Impact factor: 4.033

7.  Peptaibol zervamicin IIb structure and dynamics refinement from transhydrogen bond J couplings.

Authors:  Z O Shenkarev; T A Balashova; Z A Yakimenko; T V Ovchinnikova; A S Arseniev
Journal:  Biophys J       Date:  2004-06       Impact factor: 4.033

8.  Two classes of alamethicin transmembrane channels: molecular models from single-channel properties.

Authors:  D O Mak; W W Webb
Journal:  Biophys J       Date:  1995-12       Impact factor: 4.033

9.  Membrane orientation of the N-terminal segment of alamethicin determined by solid-state 15N NMR.

Authors:  C L North; M Barranger-Mathys; D S Cafiso
Journal:  Biophys J       Date:  1995-12       Impact factor: 4.033

10.  Structure and alignment of the membrane-associated peptaibols ampullosporin A and alamethicin by oriented 15N and 31P solid-state NMR spectroscopy.

Authors:  Evgeniy S Salnikov; Herdis Friedrich; Xing Li; Philippe Bertani; Siegmund Reissmann; Christian Hertweck; Joe D J O'Neil; Jan Raap; Burkhard Bechinger
Journal:  Biophys J       Date:  2009-01       Impact factor: 4.033

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.