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Catalysis of Ground State cis → trans Isomerization of Bacteriorhodopsin’s Retinal Chromophore by a Hydrogen-Bond Network

Journal Article · · Journal of Membrane Biology
 [1];  [2];  [3];  [4];  [5]
  1. Freie Univ., Berlin (Germany). Dept. of Physical and Theoretical Chemistry, Theoretical Molecular Biophysics, Inst. for Chemistry und Biochemistry
  2. Technische Univ. Braunschweig (Germany). Inst. of Physical and Theoretical Chemistry; BASF SE, Ludwigshafen am Rhein (Germany)
  3. Freie Univ., Berlin (Germany). Dept. of Physics, Theoretical Molecular Biophysics
  4. Karlsruhe Inst. of Technology (KIT) (Germany). Inst. for Physical Chemistry, Dept. of Theoretical Chemical Biology
  5. Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Center for Molecular Biophysics; Univ. of Tennessee, Knoxville, TN (United States). Dept. of Biochemistry and Molecular and Cellular Biology
+ Show Author Affiliations

For the photocycle of the membrane protein bacteriorhodopsin to proceed efficiently, the thermal 13-cis to all-trans back-isomerization of the retinal chromophore must return the protein to its resting state on a time-scale of milliseconds. Here, we report on quantum mechanical/molecular mechanical energy calculations examining the structural and energetic determinants of the retinal cis–trans isomerization in the protein environment. The results suggest that a hydrogen-bonded network consisting of the retinal Schiff base, active site amino acid residues, and water molecules can stabilize the twisted retinal, thus reducing the intrinsic energy cost of the cis–trans thermal isomerization barrier.

Research Organization:
Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States)
Sponsoring Organization:
USDOE
Grant/Contract Number:
AC05-00OR22725
OSTI ID:
1462860
Journal Information:
Journal of Membrane Biology, Journal Name: Journal of Membrane Biology Journal Issue: 3 Vol. 251; ISSN 0022-2631
Publisher:
SpringerCopyright Statement
Country of Publication:
United States
Language:
English

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Figures / Tables (8)

Table 1(p. 5)table Table 1
Figure 1(p. 20)figure Figure 1
Figure 2(p. 21)figure Figure 2
Figure 3(p. 22)figure Figure 3
Figure 4(p. 23)figure Figure 4
Figure 5(p. 24)figure Figure 5
Figure 6(p. 25)figure Figure 6
Table 2(p. 26)table Table 2

Similar Records

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C14-C15 single bond isomerizations of the retinal chromophore involved in the proton-pumping mechanism of bacteriorhodopsin
Journal Article · Fri Jan 31 23:00:00 EST 1986 · Proc. Natl. Acad. Sci. U.S.A.; (United States) · OSTI ID:5630052
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Related Subjects

59 BASIC BIOLOGICAL SCIENCES
Bacteriorhodopsin
Calculations
Energy
Isomerization
QM/MM
Retinal