Journal
BIOCHEMISTRY
Volume 56, Issue 16, Pages 2197-2208Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.biochem.7b00002
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Funding
- National Science Foundation [CBET-1264434]
- National Institutes of Health [R01GM027750]
- Hermann Eye Fund
- Robert A. Welch Foundation [AU-0009]
- Div Of Chem, Bioeng, Env, & Transp Sys
- Directorate For Engineering [1264434] Funding Source: National Science Foundation
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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 hands 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: hat 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.
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