» Articles » PMID: 28350445

Structural Changes in an Anion Channelrhodopsin: Formation of the K and L Intermediates at 80 K

Overview
Journal Biochemistry
Specialty Biochemistry
Date 2017 Mar 29
PMID 28350445
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

A recently discovered natural family of light-gated anion channelrhodopsins (ACRs) from cryptophyte algae provides an effective means of optogenetically silencing neurons. The most extensively studied ACR is from Guillardia theta (GtACR1). Earlier studies of GtACR1 have established a correlation between formation of a blue-shifted L-like intermediate and the anion channel "open" state. To study structural changes of GtACR1 in the K and L intermediates of the photocycle, a combination of low-temperature Fourier transform infrared (FTIR) and ultraviolet-visible absorption difference spectroscopy was used along with stable-isotope retinal labeling and site-directed mutagenesis. In contrast to bacteriorhodopsin (BR) and other microbial rhodopsins, which form only a stable red-shifted K intermediate at 80 K, GtACR1 forms both stable K and L-like intermediates. Evidence includes the appearance of positive ethylenic and fingerprint vibrational bands characteristic of the L intermediate as well as a positive visible absorption band near 485 nm. FTIR difference bands in the carboxylic acid C═O stretching region indicate that several Asp/Glu residues undergo hydrogen bonding changes at 80 K. The Glu68 → Gln and Ser97 → Glu substitutions, residues located close to the retinylidene Schiff base, altered the K:L ratio and several of the FTIR bands in the carboxylic acid region. In the case of the Ser97 → Glu substitution, a significant red-shift of the absorption wavelength of the K and L intermediates occurs. Sequence comparisons suggest that L formation in GtACR1 at 80 K is due in part to the substitution of the highly conserved Leu or Ile at position 93 in helix 3 (BR sequence) with the homologous Met105 in GtACR1.

Citing Articles

Multiple retinal isomerizations during the early phase of the bestrhodopsin photoreaction.

Kaziannis S, Broser M, van Stokkum I, Dostal J, Busse W, Munhoven A Proc Natl Acad Sci U S A. 2024; 121(12):e2318996121.

PMID: 38478688 PMC: 10962995. DOI: 10.1073/pnas.2318996121.


My remembrances of H.G. Khorana: exploring the mechanism of bacteriorhodopsin with site-directed mutagenesis and FTIR difference spectroscopy.

Rothschild K Biophys Rev. 2023; 15(1):103-110.

PMID: 36909952 PMC: 9995631. DOI: 10.1007/s12551-023-01046-9.


Rhodopsins: An Excitingly Versatile Protein Species for Research, Development and Creative Engineering.

de Grip W, Ganapathy S Front Chem. 2022; 10:879609.

PMID: 35815212 PMC: 9257189. DOI: 10.3389/fchem.2022.879609.


Proton transfer pathway in anion channelrhodopsin-1.

Tsujimura M, Kojima K, Kawanishi S, Sudo Y, Ishikita H Elife. 2021; 10.

PMID: 34930528 PMC: 8691836. DOI: 10.7554/eLife.72264.


The crystal structure of bromide-bound ACR1 reveals a pre-activated state in the transmembrane anion tunnel.

Li H, Huang C, Govorunova E, Sineshchekov O, Yi A, Rothschild K Elife. 2021; 10.

PMID: 33998458 PMC: 8172240. DOI: 10.7554/eLife.65903.


References
1.
Tajkhorshid E, Baudry J, Schulten K, Suhai S . Molecular dynamics study of the nature and origin of retinal's twisted structure in bacteriorhodopsin. Biophys J. 2000; 78(2):683-93. PMC: 1300671. DOI: 10.1016/S0006-3495(00)76626-4. View

2.
Ogren J, Mamaev S, Russano D, Li H, Spudich J, Rothschild K . Retinal chromophore structure and Schiff base interactions in red-shifted channelrhodopsin-1 from Chlamydomonas augustae. Biochemistry. 2014; 53(24):3961-70. PMC: 4072394. DOI: 10.1021/bi500445c. View

3.
Edmonds B, Luecke H . Atomic resolution structures and the mechanism of ion pumping in bacteriorhodopsin. Front Biosci. 2004; 9:1556-66. DOI: 10.2741/1264. View

4.
Muders V, Kerruth S, Lorenz-Fonfria V, Bamann C, Heberle J, Schlesinger R . Resonance Raman and FTIR spectroscopic characterization of the closed and open states of channelrhodopsin-1. FEBS Lett. 2014; 588(14):2301-6. DOI: 10.1016/j.febslet.2014.05.019. View

5.
Neumann-Verhoefen M, Neumann K, Bamann C, Radu I, Heberle J, Bamberg E . Ultrafast infrared spectroscopy on channelrhodopsin-2 reveals efficient energy transfer from the retinal chromophore to the protein. J Am Chem Soc. 2013; 135(18):6968-76. DOI: 10.1021/ja400554y. View