Literature DB >> 19431894

Evidence for unbenignant nature of glucose as a replacement for water in purple membranes.

N J Gibson1, J Y Cassim.   

Abstract

The net angle (theta(alpha)) between the seven helical segments of the bacteriorhodopsin (bR) polypeptide and the normal to the membrane plane of the purple membrane (PM) is approximately 0 degrees when determined by oriented far-ultraviolet (UV) circular dichroism (OCD) and midinfrared linear dichroism (IRLD). However, theta(alpha) is approximately 11 degrees when determined by high-resolution electron cryo-microscopy and electron diffraction (EMD). The spectral studies are made with fresh hydrated PM films at ambient temperature, whereas diffraction studies are made with aged glucose-embedded PM at -120 to -268 degrees . The current study presents oriented far-UV OCD results of hydrated PM films embedded with glucose, which can best be interpreted as a change in the magnitude of theta(alpha) (Deltatheta(alpha)) from 0 to 23 degrees as a consequence of glucose embedment. Possible alternative explanations contrary to this conclusion are discussed and ruled out. Therefore, it is suggested that a theta(alpha) of approximately 11 degrees as determined by the EMD method may not be an intrinsic structural characteristic of the native PM but an induced one. The differences in the Deltatheta(alpha) value due to glucose embedment as determined by the two different approaches (23 vs. 11 degrees ) may be attributed to the drastic differences in the experimental conditions used, especially temperature. It is expected that at extremely low temperatures protein dynamics would be highly restricted and Deltatheta(alpha) relatively curtailed. It is concluded that glucose may not be as benign to biological structures as has been assumed in the past.

Entities:  

Year:  1993        PMID: 19431894      PMCID: PMC1262468          DOI: 10.1016/S0006-3495(93)81510-8

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


  38 in total

1.  Large Scale Global Structural Changes of the Purple Membrane during the Photocycle.

Authors:  J E Draheim; J Y Cassim
Journal:  Biophys J       Date:  1985-04       Impact factor: 4.033

2.  Further characterization of protein secondary structures in purple membrane by circular dichroism and polarized infrared spectroscopies.

Authors:  E Nabedryk; A M Bardin; J Breton
Journal:  Biophys J       Date:  1985-12       Impact factor: 4.033

3.  Infrared spectrum of the purple membrane: clue to a proton conduction mechanism?

Authors:  S Krimm; A M Dwivedi
Journal:  Science       Date:  1982-04-23       Impact factor: 47.728

4.  Orientation of intrinsic proteins in photosynthetic membranes. Polarized infrared spectroscopy of chloroplasts and chromatophores.

Authors:  E Nabedryk; J Breton
Journal:  Biochim Biophys Acta       Date:  1981-05-13

5.  Fourier transform infrared difference spectroscopy of bacteriorhodopsin and its photoproducts.

Authors:  K Bagley; G Dollinger; L Eisenstein; A K Singh; L Zimányi
Journal:  Proc Natl Acad Sci U S A       Date:  1982-08       Impact factor: 11.205

6.  Projected structure of purple membrane determined to 3.7 A resolution by low temperature electron microscopy.

Authors:  S B Hayward; R M Stroud
Journal:  J Mol Biol       Date:  1981-09-25       Impact factor: 5.469

7.  Oriented secondary structure in integral membrane proteins. I. Circular dichroism and infrared spectroscopy of cytochrome oxidase in multilamellar films.

Authors:  M D Bazzi; R W Woody
Journal:  Biophys J       Date:  1985-12       Impact factor: 4.033

8.  Nature of forces stabilizing the transmembrane protein bacteriorhodopsin in purple membrane.

Authors:  N J Gibson; J Y Cassim
Journal:  Biophys J       Date:  1989-10       Impact factor: 4.033

9.  Dehydration-induced molecular structural changes of purple membrane of halobacterium halobium.

Authors:  J E Draheim; N J Gibson; J Y Cassim
Journal:  Biophys J       Date:  1988-11       Impact factor: 4.033

10.  Bacteriorhodopsin is an inside-out protein.

Authors:  D M Engelman; G Zaccai
Journal:  Proc Natl Acad Sci U S A       Date:  1980-10       Impact factor: 11.205

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