Literature DB >> 10024456

The structure of bacteriorhodopsin at 3.0 A resolution based on electron crystallography: implication of the charge distribution.

K Mitsuoka1, T Hirai, K Murata, A Miyazawa, A Kidera, Y Kimura, Y Fujiyoshi.   

Abstract

Electron crystallography has the potential to visualise the charge status of atoms. This is due to the significantly different scattering factors of neutral and ionised atoms for electrons in the low-resolution range (typically less than 5 A). In previous work, we observed two different types of densities around acidic residues in the experimental (|Fo|) map of bacteriorhodopsin (bR), a light-driven proton pump. We suggested that these might reflect different states of the acidic residues; namely, the protonated (neutral) and the deprotonated (negatively charged) state. To evaluate the observed charge more quantitatively, we refined the atomic model for bR and eight surrounding lipids using our electron crystallographic data set between 8.0 and 3.0 A resolution, where the charge effect is small. The refined model yielded an R-factor of 23.7% and a free R-factor of 33.0%. To evaluate the effect of charges on the density map, we calculated a difference (|Fo|-|Fc|) map including data of a resolution lower than 8.0 A resolution, where the charge effect is significant. We found strong peaks in the difference map mainly in the backbone region of the transmembrane helices. We interpreted these peaks to come from the polarisation of the polar groups in the main chain of the alpha-helices and we examined this by assuming a partial charge of 0.5 for the peptide carbonyl groups. The resulting R and free R-factors dropped from 0.250 and 0.341 to 0.246 and 0.336, respectively. Furthermore, we also observed some strong peaks around some side-chains, which could be assigned to positively charged atoms. Thus, we could show that Asp36 and Asp102 are likely to interact with cations nearby. In addition, peaks found around the acidic residues Glu74, Glu194 and Glu212 have different features and might represent positive charges on polarised water molecules or hydroxonium ions. Copyright 1998 Academic Press Limited.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10024456     DOI: 10.1006/jmbi.1998.2529

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  69 in total

1.  Fourier transform infrared evidence for early deprotonation of Asp(85) at alkaline pH in the photocycle of bacteriorhodopsin mutants containing E194Q.

Authors:  T Lazarova; C Sanz; E Querol; E Padrós
Journal:  Biophys J       Date:  2000-04       Impact factor: 4.033

2.  Structure of the bacteriorhodopsin mutant F219L N intermediate revealed by electron crystallography.

Authors:  J Vonck
Journal:  EMBO J       Date:  2000-05-15       Impact factor: 11.598

3.  Modeling of the structural features of integral-membrane proteins reverse-environment prediction of integral membrane protein structure (REPIMPS).

Authors:  S Dastmalchi; M B Morris; W B Church
Journal:  Protein Sci       Date:  2001-08       Impact factor: 6.725

4.  Quantitative comparison of zero-loss and conventional electron diffraction from two-dimensional and thin three-dimensional protein crystals.

Authors:  Koji Yonekura; Saori Maki-Yonekura; Keiichi Namba
Journal:  Biophys J       Date:  2002-05       Impact factor: 4.033

5.  Unfolding pathways of native bacteriorhodopsin depend on temperature.

Authors:  Harald Janovjak; Max Kessler; Dieter Oesterhelt; Hermann Gaub; Daniel J Müller
Journal:  EMBO J       Date:  2003-10-01       Impact factor: 11.598

6.  The structures of the active center in dark-adapted bacteriorhodopsin by solution-state NMR spectroscopy.

Authors:  Heiko Patzelt; Bernd Simon; Antonius terLaak; Brigitte Kessler; Ronald Kühne; Peter Schmieder; Dieter Oesterhelt; Hartmut Oschkinat
Journal:  Proc Natl Acad Sci U S A       Date:  2002-07-15       Impact factor: 11.205

7.  Robert Feulgen Lecture. Microscopic assessment of membrane protein structure and function.

Authors:  Andreas Engel
Journal:  Histochem Cell Biol       Date:  2003-07-24       Impact factor: 4.304

8.  Structural changes during the formation of early intermediates in the bacteriorhodopsin photocycle.

Authors:  Shigehiko Hayashi; Emad Tajkhorshid; Klaus Schulten
Journal:  Biophys J       Date:  2002-09       Impact factor: 4.033

9.  Stability of bacteriorhodopsin alpha-helices and loops analyzed by single-molecule force spectroscopy.

Authors:  Daniel J Müller; Max Kessler; Filipp Oesterhelt; Clemens Möller; Dieter Oesterhelt; Hermann Gaub
Journal:  Biophys J       Date:  2002-12       Impact factor: 4.033

10.  Molecular force modulation spectroscopy revealing the dynamic response of single bacteriorhodopsins.

Authors:  Harald Janovjak; Daniel J Müller; Andrew D L Humphris
Journal:  Biophys J       Date:  2004-12-01       Impact factor: 4.033

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.