Identifying and Modulating Accidental Fermi Resonance: 2D IR and DFT Study of 4‑Azido‑l‑phenylalanine
journal contributionposted on 01.08.2018, 00:00 authored by Jia Zhang, Li Wang, Jin Zhang, Jiangrui Zhu, Xin Pan, Zhifeng Cui, Jiangyun Wang, Weihai Fang, Yunliang Li
Azido-modified aromatic amino acids have been used as powerful infrared probes for the site-specific detection of proteins because of their large transition dipole strengths. However, their complex absorption profiles hinder their wider application. The complicated absorption profile of 4-azido-l-phenylalanine (pN3Phe) in isopropanol was identified and attributed to accidental Fermi resonances (FRs) by means of linear absorption and two-dimensional (2D) IR spectroscopies. The 2D IR results of pN3Phe in H2O and D2O further demonstrate that the FRs are distinctively influenced by the hydrogen-bonding environment. Under the influence of FRs, the 2D IR shape is distorted, indicating that pN3Phe is not a good candidate in spectral diffusion studies. A three-state model and first-principles calculations were used to analyze unperturbed energy levels, unveiling the FRs between the azide asymmetric stretching band and two combination bands. Furthermore, the anharmonic frequency calculations suggest that changing the substitution position of the azide group from para to meta can effectively modulate the FRs by reducing the coupling strength. This work provides a deep understanding of the FRs in azido-modified aromatic amino acids and sheds light on the modification of azido-modified amino acids for wider utilization as vibrational probes.
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4- azido-l-phenylalaninecombination bandsdiffusion studies2 D IR shapeanharmonic frequency calculationsacidhydrogen-bonding environmentthree-state model2 D IR resultspN 3 Phesite-specific detectionabsorption profileFRD 2 OFermi Resonancevibrational probesH 2 Ofirst-principles calculations2 D IRFermi resonancesazide groupsubstitution positionabsorption profilesDFT StudyIR spectroscopiesenergy levels