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Andrew Durgan Department of Chemistry & Biochemistry Gonzaga University September 24, 2009 • Introduction – Carbon-Deuterium Labeled Amino Acids – Methods: Vibrational Techniques – Infrared Spectroscopy (IR) • IR versus Raman Spectroscopy • IR Sampling • Results – IR of Ca-D Proline – 13C NMR of Proline – Calculations of Proline Conformations • Conclusion/Future Research -C-D Protein IR Spectrum O-H, C-H, N-H • • • • • Amide bands & C=C, C=O, C=N C-D frequency shifted away from unlabeled vibrations Site-specific isotopic labeling improves structural resolution C-D bonds report on their local environment Ca-D bonds report on ψ/Φ dihedral changes Deuterium labeling produces essentially no perturbation Cα D • Unique ring structure imposes backbone conformational constraints • Proline appears in many neuropeptides • cis-trans Amide isomerization is hypothesized to play a role in neuropeptide selectivity Infrared (IR) Raman Pro/Con Does not cause local heating or photodecomposition of the sample Can cause local heating or photodecomposition of the sample More accessible instrumentation Less accessible instrumentation due to laser requirement Con/Pro Spectral observations can be obscured by H2O (g) and CO2 (g) absorptions Spectral observations are not obscured by H2O (g) and CO2 (g) absorptions. Conclusion: Both spectroscopic techniques can be useful to C-D labeled amino acid investigations. • Potassium Bromide Pellets 2 mg of sample were homogenized with 80 mg of KBr • Transmission Spectra 20 µL of aqueous samples (0.050 – 1.0 M) were dispensed between CaF2 plates with a 75 mm spacer. • Scan Parameters The sample chamber was purged with N2 and 8000 scans at 4 cm-1 resolution were collected using an MCT detector. At least four absorptions related to Pro-a-d1 were readily observed at approximately 2245, 2202, 2140, and 2060 cm-1 -3 x 10 Absorbance 3 Solid: 2245 2202 2140 2060 At least 4 absorptions Solution: 2240 2199 2135 2050 2 1 0 2250 2200 2150 2100 2050 2000 -1 Wavenumber (cm ) Similar to solid sampling, at least four absorptions related to Pro-a-d1 were observed at approximately 2240, 2199, 2135, and 2050 cm-1 d b a c e c e d b a 180 160 140 120 100 80 60 40 ppm D Hsyn Cβ Cα • B3LYP/6-31G* calculations with anharmonic corrections (Gaussian 03) were used to explore frequency changes • Protonated proline was used as a model C' D-Cα-Cβ-Hsyn Dihedral D-Cα-C′-OH • The D-Ca-Cb-Hsyn and D-Ca-C'-OH Dihedral dihedrals capture the ring flip and CO2H rotation respectively 5.2 kcal/mol 5.4 kcal/mol ring flip 2239 cm-1 2225 cm-1 CO2H rotation CO2H rotation ring flip 0.5 kcal/mol 0 kcal/mol 2246 cm-1 2244 cm-1 Relative electronic energies and C-D stretching frequencies are presented. For zwitterionic Pro, only two conformations might be expected due to symmetry of the carboxylate group. A combination band at 2255 cm-1 was predicted to be in resonance with the Ca-D stretch for all four conformations. CH2 / NH2 twisting and D-Ca-N bend CH2 / NH2 twisting and H-O-C' bend 1035 cm-1 1220 cm-1 These calculations predict possible resonances associated with CH2 / NH2 twisting and/or CH2 / NH2 twisting overtones. -3 x 10 Absorbance 3 At least 4 absorptions 2 1 0 2250 2200 2150 2100 2050 2000 -1 Wavenumber (cm ) • Pro ring flipping is faster than the NMR timescale but not the IR timescale, which is consistent with the observation of multiple IR absorptions and only one set of NMR signals. • Calculations predict that the observed absorption bands arise from Pro ring flipping, resonances associated with CH2 / NH2 twisting, and possible CH2 / NH2 twisting overtones. • Specific assignments are in progress. D O D O D O - D O + + NH D D D NH3 - D D NH3 D • Trp & Phe show absorptions at 2310 / 2280 & 2275 cm-1 • Future work includes incorporating C-D labeled amino acids (Pro, Phe, & Trp) into neuropeptides (e.g. Try-Pro-Trp-Phe). • • • • • • Dr. Matthew Cremeens, Gonzaga University Christy Watson, Gonzaga University Matt Deslman, Gonzaga University Dr. Steven Corcelli, Notre Dame Gonzaga Science Research Program Howard Hughes Medical Institute