Conformational dynamics of partially denatured myoglobin studied by time-resolved electrospray mass spectrometry with online hydrogen-deuterium exchange

被引:53
|
作者
Simmons, DA
Dunn, SD
Konermann, L [1 ]
机构
[1] Univ Western Ontario, Dept Chem, London, ON N6A 5B7, Canada
[2] Univ Western Ontario, Dept Biochem, London, ON N6A 5B7, Canada
关键词
D O I
10.1021/bi034285e
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This study demonstrates the use of electrospray mass spectrometry in conjunction with rapid online mixing ("time-resolved" ESI-MS) for monitoring protein conformational dynamics under equilibrium conditions. The hydrogen/deuterium exchange (HDX) kinetics of mildly denatured myoglobin (Mb) at pD 9.3, in the presence of 27% acetonitrile, were studied with millisecond time resolution. Analytical ultracentrifugation indicates that the average protein compactness under these solvent conditions is similar to that of native holomyoglobin (hMb). The mass spectrum shows protein ions in a wide array of charge and heme binding states, indicating the presence of multiple coexisting conformations. The experimental approach used allows the HDX kinetics of all of these species to be monitored separately. A combination of EX1 and EX2 behavior was observed for hMb ions in charge states 7+ to 9+, which predominantly represent nativelike hMb in solution. The EX1 kinetics are biphasic, indicating the presence of two protein populations that undergo conformational opening events with different rate constants. The EX2 kinetics observed for nativelike hMb are biphasic as well. All other charge and heme binding states represent non-native protein conformations that are involved in rapid interconversion processes, thus leading to monoexponential EX2 kinetics with a common rate constant. Burst phase labeling for these non-native proteins occurs at 125 sites. In contrast, the nativelike protein conformation shows burst phase labeling only for 88 sites. A kinetic model is developed which is based on the assumption of three distinct (un)folding units in Mb. The model implies that the free energy landscape of the protein exhibits a major barrier. The crossing of this barrier is most likely associated with slow, cooperative opening/closing events of the heme binding pocket. Rapid conformational fluctuations on either side of the barrier give rise to the observed EX2 kinetics. Simulated HDX kinetics based on this model are in excellent agreement with the experimental data.
引用
收藏
页码:5896 / 5905
页数:10
相关论文
共 50 条
  • [41] Structural characterization of the thrombin activation of coagulation factor VIII studied by hydrogen-deuterium exchange mass spectrometry
    Faber, J. H.
    Svensson, A.
    Andersen, M. D.
    Olsen, O. H.
    Stennicke, H.
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2011, 9 : 29 - 29
  • [42] Equilibrium unfolding of metastable antitrypsin studied by hydrogen-deuterium exchange and mass spectrometry and differential scanning calorimetry
    Tsutsui, Yuko
    BIOPHYSICAL JOURNAL, 2007, : 400A - 400A
  • [43] Structural Insights into Glucan Phosphatase Dynamics Using Amide Hydrogen-Deuterium Exchange Mass Spectrometry
    Hsu, Simon
    Kim, Youngjun
    Li, Sheng
    Durrant, Eric S.
    Pace, Rachel M.
    Woods, Virgil L., Jr.
    Gentry, Matthew S.
    BIOCHEMISTRY, 2009, 48 (41) : 9891 - 9902
  • [44] Computational Tools for Hydrogen-Deuterium Exchange Mass Spectrometry Data Analysis
    Stofella, Michele
    Grimaldi, Antonio
    Smit, Jochem H.
    Claesen, Jurgen
    Paci, Emanuele
    Sobott, Frank
    CHEMICAL REVIEWS, 2024, 124 (21) : 12242 - 12263
  • [45] A simple method for differentiation of monoisotopic drug metabolites with hydrogen-deuterium exchange liquid chromatography/electrospray mass spectrometry
    Tolonen, A
    Turpeinen, M
    Uusitalo, J
    Pelkonen, O
    EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2005, 25 (01) : 155 - 162
  • [46] Characterization of Ceramides with Phytosphingosine Backbone by Hydrogen-deuterium Exchange Mass Spectrometry
    Dapic, Irena
    Brkljacic, Lidija
    Jakasa, Ivone
    Kobetic, Renata
    CROATICA CHEMICA ACTA, 2019, 92 (03) : 411 - 417
  • [47] Determination of the conformation of human α-crystallin by hydrogen-deuterium exchange/mass spectrometry
    Smith, JB
    Hasan, A
    Yu, J
    Smith, DL
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2000, 41 (04) : S582 - S582
  • [48] Dimerization interface of osteoprotegerin revealed by hydrogen-deuterium exchange mass spectrometry
    Xiao, Yiming
    Li, Miaomiao
    Larocque, Rinzhi
    Zhang, Fuming
    Malhotra, Anju
    Chen, Jianle
    Linhardt, Robert J.
    Konermann, Lars
    Xu, Ding
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2018, 293 (45) : 17523 - 17535
  • [49] Hydrogen-deuterium exchange mass spectrometry of membrane proteins in lipid nanodiscs
    Redhair, Michelle
    Clouser, Amanda F.
    Atkins, William M.
    CHEMISTRY AND PHYSICS OF LIPIDS, 2019, 220 : 14 - 22
  • [50] Conformational dynamics of GW182 silencing domain and CNOT1 fragment as monitored by hydrogen-deuterium exchange mass spectrometry
    Cieplak-Rotowska, M. K.
    Tarnowski, K.
    Dadlez, M.
    Fabian, M. R.
    Sonenberg, N.
    Darzynkiewicz, E.
    Niedzwiecka, A.
    FEBS JOURNAL, 2015, 282 : 332 - 332