Heteronuclear Adiabatic Relaxation Dispersion (HARD) for quantitative analysis of conformational dynamics in proteins

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• 作者：Nathaniel J. Traaseth^a ; ^e ; Fa-An Chao^a ; Larry R. Masterson^a ; Silvia Mangia^c ; Michael Garwood^c ; Shalom Michaeli^c ; Burckhard Seelig^a ; ^d ; Gianluigi Veglia^a ; ^b ; ^{vegli001@umn.edu}
• 关键词：HARD ; Heteronuclear Adiabatic Relaxation Dispersion ; CPMG ; Carr&ndash ; Purcell&ndash ; Meiboom&ndash ; Gill ; R1蟻 ; longitudinal rotating frame relaxation rate constant ; R2蟻 ; transverse rotating frame relaxation rate constant
• 刊名：Journal of Magnetic Resonance
• 出版年：2012
• 期刊代码：126_10907807
• 类别：ch
• 出版时间：June, 2012
• 卷：219
• 期：Complete
• 页码：75-82
• 文件大小：876 K

摘要

NMR relaxation methods probe biomolecular motions over a wide range of timescales. In particular, the rotating frame spin-lock R_1蟻 and Carr-Purcell-Meiboom-Gill (CPMG) R₂ experiments are commonly used to characterize 渭s to ms dynamics, which play a critical role in enzyme folding and catalysis. In an effort to complement these approaches, we introduced the Heteronuclear Adiabatic Relaxation Dispersion (HARD) method, where dispersion in rotating frame relaxation rate constants (longitudinal R_1蟻 and transverse R_2蟻) is created by modulating the shape and duration of adiabatic full passage (AFP) pulses. Previously, we showed the ability of the HARD method to detect chemical exchange dynamics in the fast exchange regime (k_ex 鈭?#xA0;10⁴-10⁵ s^鈭?). In this article, we show the sensitivity of the HARD method to slower exchange processes by measuring R_1蟻 and R_2蟻 relaxation rates for two soluble proteins (ubiquitin and 10C RNA ligase). One advantage of the HARD method is its nominal dependence on the applied radio frequency field, which can be leveraged to modulate the dispersion in the relaxation rate constants. In addition, we also include product operator simulations to define the dynamic range of adiabatic R_1蟻 and R_2蟻 that is valid under all exchange regimes. We conclude from both experimental observations and simulations that this method is complementary to CPMG-based and rotating frame spin-lock R_1蟻 experiments to probe conformational exchange dynamics for biomolecules. Finally, this approach is germane to several NMR-active nuclei, where relaxation rates are frequency-offset independent.