Using 2D-IR Spectroscopy to Measure the Structure, Dynamics, and Intermolecular Interactions of Proteins in H₂O

Abstract

Metrics & MoreArticle Recommendations CONSPECTUS: Infrared (IR) spectroscopy probes molecular structure at the level of the chemical bond or functional group. In the case of proteins, the most informative band in the IR spectrum is the amide I band, which arises predominantly from the C�O stretching vibration of the peptide link. The folding of proteins into secondary and tertiary structures leads to vibrational coupling between peptide units, generating specific amide I spectral signatures that provide a fingerprint of the macromolecular conformation. Ultrafast two-dimensional IR (2D-IR) spectroscopy allows the amide I band of a protein to be spread over a second frequency dimension in a way that mirrors 2D-NMR methods. This means that amide I 2D-IR spectroscopy produces a spectral map that is exquisitely sensitive to protein structure and dynamics and so provides detailed insights that cannot be matched by IR absorption spectroscopy. As a result, 2D-IR spectroscopy has emerged as a powerful tool for probing protein structure and dynamics over a broad range of time and length scales in the solution phase at room temperature. However, the protein amide I band coincides with an IR absorption from the bending vibration of water (δ HOH ), the natural biological solvent. To circumvent this problem, protein IR studies are routinely performed in D 2 O solutions because H/D substitution shifts the solvent bending mode (δ DOD ) to a lower frequency, revealing the amide I band. While effective, this method raises fundamental questions regarding the impact of the change in solvent mass on the structural or solvation dynamics of the protein and the removal of the energetic resonance between solvent and solute.In this Account, a series of studies applying 2D-IR to study the spectroscopy and dynamics of proteins in H 2 O-rich solvents is reviewed. A comparison of IR absorption spectroscopy and 2D-IR spectroscopy of protein-containing fluids is used to demonstrate the basis of the approach before a series of applications is presented. These range from measurements of fundamental protein biophysics to recent applications of machine learning to gain insight into protein−drug binding in complex mixtures. An outlook is presented, considering the potential for 2D-IR measurements to contribute to our understanding of protein behavior under nearphysiological conditions, along with an evaluation of the obstacles that still need to be overcome.

Poly(l-threonine-co-l-threonine Succinate) Thermogels for Sustained Release of Lixisenatide

“…The major amide I band of the PTTs was observed at 1620 cm –1 , indicating that the β-sheet is the major secondary structure of PTTs (Figure b). D 2 O was used as the solvent because the vibrational frequency of the H 2 O bending mode overlaps in this region, whereas that of D 2 O is observed at 1100–1300, and does not interfere with the interpretation of the amide I band. , As the temperature increased from 20 to 50 °C, the ratio of absorbance at 1620 to 1454 cm –1 increased, suggesting that the β-sheet content partially increased during the sol-to-gel transition (Figure b inset) . In addition, 1 H NMR spectra were also monitored as the temperature increased from 20 to 50 °C.…”