Optimization of cross-polarization at low radiofrequency fields for sensitivity enhancement in solid-state NMR of membrane proteins reconstituted in magnetically aligned bicelles
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作者:
Koroloff, Sophie N.
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N Carolina State Univ, Dept Chem, Raleigh, NC 27695 USAN Carolina State Univ, Dept Chem, Raleigh, NC 27695 USA
Koroloff, Sophie N.
[1
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Nevzorov, Alexander A.
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N Carolina State Univ, Dept Chem, Raleigh, NC 27695 USAN Carolina State Univ, Dept Chem, Raleigh, NC 27695 USA
Nevzorov, Alexander A.
[1
]
机构:
[1] N Carolina State Univ, Dept Chem, Raleigh, NC 27695 USA
Solid-state NMR (ssNMR) of oriented membrane proteins (MPs) is capable of providing structural and dynamic information at nearly physiological conditions. However, NMR experiments performed on oriented membrane proteins generally suffer from low sensitivity. Moreover, utilization of high-power radiofrequency (RF) irradiations for magnetization transfer may give rise to sample heating, thereby decreasing the efficiency of conventional cross-polarization schemes. Here we have optimized the recently developed repetitive cross-polarization (REP-CP) sequence (Tang et al., 2011) to further increase the magnetization transfer efficiency for membrane proteins reconstituted in magnetically aligned bicelles and compared its performance to single-contact Hartmann-Hahn cross-polarization (CP), CP-MOIST and the adiabatic transfer. It has been found that employing the REP-CP sequence at RF amplitudes of 19 kHz instead of the commonly used higher RF fields (>45 kHz) enhances the efficiency of REP-CP. An additional 30% signal can be obtained as compared to the previously published REP-CP, and 20% when compared to the re-optimized REP-CP at 50 kHz RF fields. Moreover, the N-55 signal gain of low-power REP-CP was found to be 40% over the adiabatic CP and up to 80% over CP-MOIST. Thus, the low-power REP-CP sequence surpasses all of the previous CP schemes in addition of having the tremendous advantage of reducing the RF powers by a factor of seven, thereby preserving the liquid-like bicelle sample. By contrast, in purely static (NAL crystal) and semi-rigid systems (Pf1 phage), the adiabatic CP was found to be more effective. Periodic oscillations of the intensity profile (distinct from the transient oscillations) as a function of the CP contact time and B-1 RF field strengths were observed during the REP-CP optimization with the oscillations becoming more pronounced with lower RF fields. Many-spin simulations were performed to explain the oscillations and their periodicity. (C) 2015 Elsevier Inc. All rights reserved.
机构:
JEOL Beijing Co Ltd, Beijing 100190, Peoples R China
JEOL RESONANCE Inc, Akishima, Tokyo 1968558, JapanJEOL Beijing Co Ltd, Beijing 100190, Peoples R China
Ye, Yue-Qi
Martineau-Corcos, Charlotte
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Univ Versailles St Quentin En Yvelines, CNRS UMR8180, Inst Lavoisier Versailles, 45 Ave Etats Unis, F-78035 Versailles, France
Univ Orleans, CNRS, CEMHTI UPR3079, F-45071 Orleans, FranceJEOL Beijing Co Ltd, Beijing 100190, Peoples R China
Martineau-Corcos, Charlotte
Taulelle, Francis
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机构:
Univ Versailles St Quentin En Yvelines, CNRS UMR8180, Inst Lavoisier Versailles, 45 Ave Etats Unis, F-78035 Versailles, France
Katholieke Univ Leuven, Ctr Surface Chem & Catalysis, Celestijnenlaan 200F Box 2461, B-3001 Leuven, BelgiumJEOL Beijing Co Ltd, Beijing 100190, Peoples R China
Taulelle, Francis
Nishiyama, Yusuke
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机构:
JEOL RESONANCE Inc, Akishima, Tokyo 1968558, Japan
RIKEN JEOL Collaborat Ctr, Yokohama, Kanagawa 2300045, JapanJEOL Beijing Co Ltd, Beijing 100190, Peoples R China
机构:
US DOE, Ames Lab, Ames, IA 50011 USAUS DOE, Ames Lab, Ames, IA 50011 USA
Kobayashi, Takeshi
Lafon, Olivier
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机构:
Univ Lille Nord de France, F-59000 Lille, France
Univ Lille 1, Ecole Natl Super Chim Lille, CNRS, Unite Catalyse & Chim Solide,UMR 8181, F-59652 Villeneuve Dascq, FranceUS DOE, Ames Lab, Ames, IA 50011 USA
Lafon, Olivier
Thankamony, Aany S. Lilly
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机构:
Univ Lille Nord de France, F-59000 Lille, France
Univ Lille 1, Ecole Natl Super Chim Lille, CNRS, Unite Catalyse & Chim Solide,UMR 8181, F-59652 Villeneuve Dascq, FranceUS DOE, Ames Lab, Ames, IA 50011 USA
Thankamony, Aany S. Lilly
Slowing, Igor I.
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US DOE, Ames Lab, Ames, IA 50011 USAUS DOE, Ames Lab, Ames, IA 50011 USA
Slowing, Igor I.
Kandel, Kapil
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US DOE, Ames Lab, Ames, IA 50011 USA
Iowa State Univ, Dept Chem, Ames, IA 50011 USAUS DOE, Ames Lab, Ames, IA 50011 USA
机构:
Univ Lille Nord de France, F-59000 Lille, France
Univ Lille 1, Lab Spectrochim Infrarouge & Raman LASIR, CNRS, UMR 8516, F-59652 Villeneuve Dascq, FranceUS DOE, Ames Lab, Ames, IA 50011 USA
Vezin, Herve
Amoureux, Jean-Paul
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机构:
Univ Lille Nord de France, F-59000 Lille, France
Univ Lille 1, Ecole Natl Super Chim Lille, CNRS, Unite Catalyse & Chim Solide,UMR 8181, F-59652 Villeneuve Dascq, FranceUS DOE, Ames Lab, Ames, IA 50011 USA
Amoureux, Jean-Paul
Bodenhausen, Geoffrey
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机构:
Ecole Polytech Fed Lausanne, EPFL, Inst Sci & Ingn Chim, CH-1015 Lausanne, Switzerland
Univ Paris 06, CNRS, UMR 7203, Ecole Normale Super,Dept Chim, Paris, FranceUS DOE, Ames Lab, Ames, IA 50011 USA
Bodenhausen, Geoffrey
Pruski, Marek
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US DOE, Ames Lab, Ames, IA 50011 USA
Iowa State Univ, Dept Chem, Ames, IA 50011 USAUS DOE, Ames Lab, Ames, IA 50011 USA
机构:
Univ Tokyo, Grad Sch Agr & Life Sci, Bunkyo Ku, Tokyo 1138657, JapanUniv Tokyo, Grad Sch Agr & Life Sci, Bunkyo Ku, Tokyo 1138657, Japan
Fujisawa, Shuji
Kobayashi, Kayoko
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Kyoto Univ, Div Forest & Biomat Sci, Grad Sch Agr, Sakyo Ku, Kyoto 6068502, JapanUniv Tokyo, Grad Sch Agr & Life Sci, Bunkyo Ku, Tokyo 1138657, Japan
Kobayashi, Kayoko
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Saito, Tsuguyuki
Ashida, Jun
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机构:
JEOL Ltd, Chiyoda Ku, Tokyo 1000004, JapanUniv Tokyo, Grad Sch Agr & Life Sci, Bunkyo Ku, Tokyo 1138657, Japan