7spx
Crystal structure of photoactive yellow protein (PYP); F28oCNF constructCrystal structure of photoactive yellow protein (PYP); F28oCNF construct
Structural highlights
FunctionPYP_HALHA Photoactive blue light protein. Probably functions as a photoreceptor for a negative phototaxis response. Publication Abstract from PubMedNitriles are widely used vibrational probes; however, the interpretation of their IR frequencies is complicated by hydrogen bonding (H-bonding) in protic environments. We report a new vibrational Stark effect (VSE) that correlates the electric field projected on the -C identical withN bond to the transition dipole moment and, by extension, the nitrile peak area or integrated intensity. This linear VSE applies to both H-bonding and non-H-bonding interactions. It can therefore be generally applied to determine electric fields in all environments. Additionally, it allows for semiempirical extraction of the H-bonding contribution to the blueshift of the nitrile frequency. Nitriles were incorporated at H-bonding and non-H-bonding protein sites using amber suppression, and each nitrile variant was structurally characterized at high resolution. We exploited the combined information available from variations in frequency and integrated intensity and demonstrate that nitriles are a generally useful probe for electric fields. Nitrile Infrared Intensities Characterize Electric Fields and Hydrogen Bonding in Protic, Aprotic, and Protein Environments.,Weaver JB, Kozuch J, Kirsh JM, Boxer SG J Am Chem Soc. 2022 May 4;144(17):7562-7567. doi: 10.1021/jacs.2c00675. Epub 2022, Apr 25. PMID:35467853[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
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