タンパク質における量子メチル・トンネリング周波数の直接観測と測定:Tm編集二重電子間電子共鳴EPR分光法を用いて
Thomas Schmidt1, Francesco Torricella1, G Marius Clore1
1Laboratory of Chemical Physics, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892-0520, USA. thomas.schmidt@nih.gov.
Abstract:
Using a leucine methyl protonated, otherwise fully deuterated, {U[2H]; [Leu-[13CH3]}, isotopically labeled model protein, spin-labeled at two sites with the rigid R1p nitroxide sidechain, one of which is present in two distinct conformers, we show that the oscillations in the ratio of integrated intensities of the two peaks in the double electron-electron resonance (DEER)-derived probability distance distribution as a function of the second echo period time T in a series of Tm-edited DEER experiments arise from methyl tunnelling spin echo envelope modulation. Quantitative analysis yields an average methyl tunneling rate of 0.12 MHz, indicative of a high rotational barrier. These data provide the first direct observation of methyl tunneling in a protein by electron paramagnetic resonance.
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