Literature DB >> 15894635

Two-photon absorption of bacteriorhodopsin: formation of a red-shifted thermally stable photoproduct F620.

Thorsten Fischer1, Norbert A Hampp.   

Abstract

By means of high-intensity 532 nm laser pulses, a photochemical conversion of the initial B(570) state of bacteriorhodopsin (BR) to a stable photoproduct absorbing maximally at approximately 620 nm in BR suspensions and at approximately 610 nm in BR films is induced. This state, which we named F(620), is photochemically further converted to a group of three products with maximal absorptions in the wavelength range from 340 nm to 380 nm, which show identical spectral properties to the so-called P(360) state reported in the literature. The photoconversion from B(570) to F(620) is most likely a resonant two-photon absorption induced step. The formation of F(620) and P(360) leads to a distinguished photo-induced permanent optical anisotropy in BR films. The spectral dependence of the photo-induced anisotropy and the anisotropy orientations at the educt (B(570)) and product (F(620)) wavelengths are strong indicators that F(620) is formed in a direct photochemical step from B(570). The chemical nature of the P(360) products probably is that of a retro-retinal containing BR, but the structural characteristics of the F(620) state are still unclear. The photo-induced permanent anisotropy induced by short laser pulses in BR films helps to better understand the photochemical pathways related to this transition, and it is interesting in view of potential applications as this feature is the molecular basis for permanent optical data storage using BR films.

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Year:  2005        PMID: 15894635      PMCID: PMC1366602          DOI: 10.1529/biophysj.104.055806

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


  8 in total

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Authors:  C H Chang; R Jonas; S Melchiore; R Govindjee; T G Ebrey
Journal:  Biophys J       Date:  1986-03       Impact factor: 4.033

2.  Quantum efficiency of the photochemical cycle of bacteriorhodopsin.

Authors:  R Govindjee; S P Balashov; T G Ebrey
Journal:  Biophys J       Date:  1990-09       Impact factor: 4.033

3.  Early picosecond events in the photocycle of bacteriorhodopsin.

Authors:  H J Polland; M A Franz; W Zinth; W Kaiser; E Kölling; D Oesterhelt
Journal:  Biophys J       Date:  1986-03       Impact factor: 4.033

4.  The laser-induced blue state of bacteriorhodopsin: mechanistic and color regulatory roles of protein-protein interactions, protein-lipid interactions, and metal ions.

Authors:  Mark B Masthay; David M Sammeth; Merritt C Helvenston; Charles B Buckman; Wuyi Li; Michael J Cde-Baca; John T Kofron
Journal:  J Am Chem Soc       Date:  2002-04-03       Impact factor: 15.419

5.  Photocycles of bacteriorhodopsin in light- and dark-adapted purple membrane studied by time-resolved absorption spectroscopy.

Authors:  J Hofrichter; E R Henry; R H Lozier
Journal:  Biophys J       Date:  1989-10       Impact factor: 4.033

6.  Photochemical conversion of the O-intermediate to 9-cis-retinal-containing products in bacteriorhodopsin films.

Authors:  A Popp; M Wolperdinger; N Hampp; C Brüchle; D Oesterhelt
Journal:  Biophys J       Date:  1993-10       Impact factor: 4.033

7.  Salt and pH-dependent changes of the purple membrane absorption spectrum.

Authors:  Y Kimura; A Ikegami; W Stoeckenius
Journal:  Photochem Photobiol       Date:  1984-11       Impact factor: 3.421

8.  Rhodopsin-like protein from the purple membrane of Halobacterium halobium.

Authors:  D Oesterhelt; W Stoeckenius
Journal:  Nat New Biol       Date:  1971-09-29
  8 in total
  1 in total

1.  Two bathointermediates of the bacteriorhodopsin photocycle, from time-resolved nanosecond spectra in the visible.

Authors:  Andrei K Dioumaev; Janos K Lanyi
Journal:  J Phys Chem B       Date:  2009-12-31       Impact factor: 2.991

  1 in total

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