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  1. Article ; Online: Polarizing agents and mechanisms for high-field dynamic nuclear polarization of frozen dielectric solids.

    Hu, Kan-Nian

    Solid state nuclear magnetic resonance

    2011  Volume 40, Issue 2, Page(s) 31–41

    Abstract: This article provides an overview of polarizing mechanisms involved in high-frequency dynamic nuclear polarization (DNP) of frozen biological samples at temperatures maintained using liquid nitrogen, compatible with contemporary magic-angle spinning (MAS) ...

    Abstract This article provides an overview of polarizing mechanisms involved in high-frequency dynamic nuclear polarization (DNP) of frozen biological samples at temperatures maintained using liquid nitrogen, compatible with contemporary magic-angle spinning (MAS) nuclear magnetic resonance (NMR). Typical DNP experiments require unpaired electrons that are usually exogenous in samples via paramagnetic doping with polarizing agents. Thus, the resulting nuclear polarization mechanism depends on the electron and nuclear spin interactions induced by the paramagnetic species. The Overhauser Effect (OE) DNP, which relies on time-dependent spin-spin interactions, is excluded from our discussion due the lack of conducting electrons in frozen aqueous solutions containing biological entities. DNP of particular interest to us relies primarily on time-independent, spin-spin interactions for significant electron-nucleus polarization transfer through mechanisms such as the Solid Effect (SE), the Cross Effect (CE) or Thermal Mixing (TM), involving one, two or multiple electron spins, respectively. Derived from monomeric radicals initially used in high-field DNP experiments, bi- or multiple-radical polarizing agents facilitate CE/TM to generate significant NMR signal enhancements in dielectric solids at low temperatures (<100 K). For example, large DNP enhancements (∼300 times at 5 T) from a biologically compatible biradical, 1-(TEMPO-4-oxy)-3-(TEMPO-4-amino)propan-2-ol (TOTAPOL), have enabled high-resolution MAS NMR in sample systems existing in submicron domains or embedded in larger biomolecular complexes. The scope of this review is focused on recently developed DNP polarizing agents for high-field applications and leads up to future developments per the CE DNP mechanism. Because DNP experiments are feasible with a solid-state microwave source when performed at <20K, nuclear polarization using lower microwave power (<100 mW) is possible by forcing a high proportion of biradicals to fulfill the frequency matching condition of CE (two EPR frequencies separated by the NMR frequency) using the strategies involving hetero-radical moieties and/or molecular alignment. In addition, the combination of an excited triplet and a stable radical might provide alternative DNP mechanisms without the microwave requirement.
    MeSH term(s) Electric Impedance ; Freezing ; Magnetic Phenomena ; Magnetic Resonance Spectroscopy/methods ; Photochemical Processes
    Language English
    Publishing date 2011-08-06
    Publishing country Netherlands
    Document type Journal Article ; Research Support, N.I.H., Intramural ; Review
    ZDB-ID 1122088-0
    ISSN 1527-3326 ; 0926-2040
    ISSN (online) 1527-3326
    ISSN 0926-2040
    DOI 10.1016/j.ssnmr.2011.08.001
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: A Monte Carlo/simulated annealing algorithm for sequential resonance assignment in solid state NMR of uniformly labeled proteins with magic-angle spinning.

    Tycko, Robert / Hu, Kan-Nian

    Journal of magnetic resonance (San Diego, Calif. : 1997)

    2010  Volume 205, Issue 2, Page(s) 304–314

    Abstract: We describe a computational approach to sequential resonance assignment in solid state NMR studies of uniformly (15)N,(13)C-labeled proteins with magic-angle spinning. As input, the algorithm uses only the protein sequence and lists of (15)N/(13)C(alpha) ...

    Abstract We describe a computational approach to sequential resonance assignment in solid state NMR studies of uniformly (15)N,(13)C-labeled proteins with magic-angle spinning. As input, the algorithm uses only the protein sequence and lists of (15)N/(13)C(alpha) crosspeaks from 2D NCACX and NCOCX spectra that include possible residue-type assignments of each crosspeak. Assignment of crosspeaks to specific residues is carried out by a Monte Carlo/simulated annealing algorithm, implemented in the program MC_ASSIGN1. The algorithm tolerates substantial ambiguity in residue-type assignments and coexistence of visible and invisible segments in the protein sequence. We use MC_ASSIGN1 and our own 2D spectra to replicate and extend the sequential assignments for uniformly-labeled HET-s(218-289) fibrils previously determined manually by Siemer et al. (J. Biomol. NMR, 34 (2006) 75-87) from a more extensive set of 2D and 3D spectra. Accurate assignments by MC_ASSIGN1 do not require data that are of exceptionally high quality. Use of MC_ASSIGN1 (and its extensions to other types of 2D and 3D data) is likely to alleviate many of the difficulties and uncertainties associated with manual resonance assignments in solid state NMR studies of uniformly labeled proteins, where spectral resolution and signal-to-noise are often sub-optimal.
    MeSH term(s) Algorithms ; Amino Acids/chemistry ; Ammonia/chemistry ; Data Interpretation, Statistical ; Isotope Labeling ; Magnetic Resonance Spectroscopy/methods ; Magnetic Resonance Spectroscopy/statistics & numerical data ; Monte Carlo Method ; Proteins/chemistry
    Chemical Substances Amino Acids ; Proteins ; Ammonia (7664-41-7)
    Language English
    Publishing date 2010-05-25
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Intramural
    ZDB-ID 1469665-4
    ISSN 1096-0856 ; 1557-8968 ; 1090-7807 ; 0022-2364
    ISSN (online) 1096-0856 ; 1557-8968
    ISSN 1090-7807 ; 0022-2364
    DOI 10.1016/j.jmr.2010.05.013
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: What can solid state NMR contribute to our understanding of protein folding?

    Hu, Kan-Nian / Tycko, Robert

    Biophysical chemistry

    2010  Volume 151, Issue 1-2, Page(s) 10–21

    Abstract: Complete understanding of the folding process that connects a structurally disordered state of a protein to an ordered, biochemically functional state requires detailed characterization of intermediate structural states with high resolution and site ... ...

    Abstract Complete understanding of the folding process that connects a structurally disordered state of a protein to an ordered, biochemically functional state requires detailed characterization of intermediate structural states with high resolution and site specificity. While the intrinsically inhomogeneous and dynamic nature of unfolded and partially folded states limits the efficacy of traditional X-ray diffraction and solution NMR in structural studies, solid state NMR methods applied to frozen solutions can circumvent the complications due to molecular motions and conformational exchange encountered in unfolded and partially folded states. Moreover, solid state NMR methods can provide both qualitative and quantitative structural information at the site-specific level, even in the presence of structural inhomogeneity. This article reviews relevant solid state NMR methods and their initial applications to protein folding studies. Using either chemical denaturation to prepare unfolded states at equilibrium or a rapid freezing apparatus to trap non-equilibrium, transient structural states on a sub-millisecond time scale, recent results demonstrate that solid state NMR can contribute essential information about folding processes that is not available from more familiar biophysical methods.
    MeSH term(s) Nuclear Magnetic Resonance, Biomolecular ; Protein Conformation ; Protein Denaturation ; Protein Folding ; Proteins/chemistry
    Chemical Substances Proteins
    Language English
    Publishing date 2010-05-23
    Publishing country Netherlands
    Document type Journal Article ; Research Support, N.I.H., Intramural ; Review
    ZDB-ID 185052-0
    ISSN 1873-4200 ; 0301-4622
    ISSN (online) 1873-4200
    ISSN 0301-4622
    DOI 10.1016/j.bpc.2010.05.009
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Zero-quantum frequency-selective recoupling of homonuclear dipole-dipole interactions in solid state nuclear magnetic resonance.

    Hu, Kan-Nian / Tycko, Robert

    The Journal of chemical physics

    2009  Volume 131, Issue 4, Page(s) 45101

    Abstract: We describe a method for measuring magnetic dipole-dipole interactions, and hence distances, between pairs of like nuclear spins in a many-spin system under magic-angle spinning (MAS). This method employs a homonuclear dipolar recoupling sequence that ... ...

    Abstract We describe a method for measuring magnetic dipole-dipole interactions, and hence distances, between pairs of like nuclear spins in a many-spin system under magic-angle spinning (MAS). This method employs a homonuclear dipolar recoupling sequence that creates an average dipole-dipole coupling Hamiltonian under MAS with full zero-quantum symmetry, including both secular and flip-flop terms. Flip-flop terms are then attenuated by inserting rotor-synchronized periods of chemical shift evolution between recoupling blocks, leaving an effective Hamiltonian that contains only secular terms to a good approximation. Couplings between specific pairs of nuclear spins can then be selected with frequency-selective pi pulses. We demonstrate this technique, which we call zero-quantum shift evolution assisted homonuclear recoupling, in a series of one-dimensional and two-dimensional (13)C NMR experiments at 17.6 T and 40.00 kHz MAS frequency on uniformly (13)C-labeled L-threonine powder and on the helix-forming peptide MB(i+4)EK, synthesized with a pair of uniformly (13)C-labeled L-alanine residues. Experimental demonstrations include measurements of distances between (13)C sites that are separated by three bonds, placing quantitative constraints on both sidechain and backbone torsion angles in polypeptides.
    MeSH term(s) Magnetic Resonance Spectroscopy/methods ; Quantum Theory ; Threonine/chemistry
    Chemical Substances Threonine (2ZD004190S)
    Language English
    Publishing date 2009-08-05
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Intramural
    ZDB-ID 3113-6
    ISSN 1089-7690 ; 0021-9606
    ISSN (online) 1089-7690
    ISSN 0021-9606
    DOI 10.1063/1.3176874
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: A general Monte Carlo/simulated annealing algorithm for resonance assignment in NMR of uniformly labeled biopolymers.

    Hu, Kan-Nian / Qiang, Wei / Tycko, Robert

    Journal of biomolecular NMR

    2011  Volume 50, Issue 3, Page(s) 267–276

    Abstract: We describe a general computational approach to site-specific resonance assignments in multidimensional NMR studies of uniformly (15)N,(13)C-labeled biopolymers, based on a simple Monte Carlo/simulated annealing (MCSA) algorithm contained in the program ... ...

    Abstract We describe a general computational approach to site-specific resonance assignments in multidimensional NMR studies of uniformly (15)N,(13)C-labeled biopolymers, based on a simple Monte Carlo/simulated annealing (MCSA) algorithm contained in the program MCASSIGN2. Input to MCASSIGN2 includes lists of multidimensional signals in the NMR spectra with their possible residue-type assignments (which need not be unique), the biopolymer sequence, and a table that describes the connections that relate one signal list to another. As output, MCASSIGN2 produces a high-scoring sequential assignment of the multidimensional signals, using a score function that rewards good connections (i.e., agreement between relevant sets of chemical shifts in different signal lists) and penalizes bad connections, unassigned signals, and assignment gaps. Examination of a set of high-scoring assignments from a large number of independent runs allows one to determine whether a unique assignment exists for the entire sequence or parts thereof. We demonstrate the MCSA algorithm using two-dimensional (2D) and three-dimensional (3D) solid state NMR spectra of several model protein samples (α-spectrin SH3 domain and protein G/B1 microcrystals, HET-s(218-289) fibrils), obtained with magic-angle spinning and standard polarization transfer techniques. The MCSA algorithm and MCASSIGN2 program can accommodate arbitrary combinations of NMR spectra with arbitrary dimensionality, and can therefore be applied in many areas of solid state and solution NMR.
    MeSH term(s) Algorithms ; Biopolymers/chemistry ; Magnetic Resonance Spectroscopy/methods
    Chemical Substances Biopolymers
    Language English
    Publishing date 2011-06-28
    Publishing country Netherlands
    Document type Journal Article ; Research Support, N.I.H., Intramural
    ZDB-ID 1081696-3
    ISSN 1573-5001 ; 0925-2738
    ISSN (online) 1573-5001
    ISSN 0925-2738
    DOI 10.1007/s10858-011-9517-1
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Organic Arsenic in the Soil Environment: Speciation, Occurrence, Transformation, and Adsorption Behavior

    Huang, Jen-How / Hu, Kan-Nian / Decker, Berryinne

    Water, air and soil pollution. 2011 July, v. 219, no. 1-4

    2011  

    Abstract: An attempt is made to describe the fate and behavior of organic arsenic (As) compounds in the soil environment, based on an extensive literature researches. The objective of this review is to provide an overview on the state of knowledge to date about ... ...

    Abstract An attempt is made to describe the fate and behavior of organic arsenic (As) compounds in the soil environment, based on an extensive literature researches. The objective of this review is to provide an overview on the state of knowledge to date about the occurrence and potential transformation of organic As, including methylation, degradation, and hydration, in soils and their uptake and accumulation in plants and animals. Accordingly, the biogeochemical cycle of organic As in the soil environment is proposed.
    Keywords adsorption ; animals ; arsenic ; biogeochemical cycles ; edaphic factors ; methylation ; organic soils
    Language English
    Dates of publication 2011-07
    Size p. 401-415.
    Publishing place Springer-Verlag
    Document type Article
    ZDB-ID 120499-3
    ISSN 1573-2932 ; 0049-6979 ; 0043-1168
    ISSN (online) 1573-2932
    ISSN 0049-6979 ; 0043-1168
    DOI 10.1007/s11270-010-0716-2
    Database NAL-Catalogue (AGRICOLA)

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  7. Article ; Online: Detection of a transient intermediate in a rapid protein folding process by solid-state nuclear magnetic resonance.

    Hu, Kan-Nian / Yau, Wai-Ming / Tycko, Robert

    Journal of the American Chemical Society

    2009  Volume 132, Issue 1, Page(s) 24–25

    Abstract: We describe the use of solid-state NMR spectroscopy to characterize a partially folded state of the 35-residue helical protein HP35 created by rapid freeze-quenching from a thermally unfolded state on the 10-20 micros time scale. Two-dimensional solid- ... ...

    Abstract We describe the use of solid-state NMR spectroscopy to characterize a partially folded state of the 35-residue helical protein HP35 created by rapid freeze-quenching from a thermally unfolded state on the 10-20 micros time scale. Two-dimensional solid-state (13)C NMR spectra of (13)C-labeled HP35 in frozen glycerol/water solution exhibit two sets of signals, one corresponding to strongly unfolded protein molecules and the other to an ensemble of molecules having native helical secondary structure but incomplete tertiary structure. The NMR data indicate that secondary structure forms within the freeze-quenching time scale but that full folding involves a slower phase of structural annealing. The approximately 5 micros folding time observed in earlier studies of HP35 by time-resolved optical techniques may not represent the time scale for full folding.
    MeSH term(s) Freezing ; Kinetics ; Magnetic Resonance Spectroscopy ; Models, Molecular ; Neurofilament Proteins/chemistry ; Peptide Fragments/chemistry ; Protein Denaturation ; Protein Folding ; Protein Structure, Secondary ; Protein Structure, Tertiary
    Chemical Substances Neurofilament Proteins ; Peptide Fragments ; villin headpiece subdomain peptide
    Language English
    Publishing date 2009-12-09
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Intramural
    ZDB-ID 3155-0
    ISSN 1520-5126 ; 0002-7863
    ISSN (online) 1520-5126
    ISSN 0002-7863
    DOI 10.1021/ja908471n
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Quantum mechanical theory of dynamic nuclear polarization in solid dielectrics.

    Hu, Kan-Nian / Debelouchina, Galia T / Smith, Albert A / Griffin, Robert G

    The Journal of chemical physics

    2011  Volume 134, Issue 12, Page(s) 125105

    Abstract: Microwave driven dynamic nuclear polarization (DNP) is a process in which the large polarization present in an electron spin reservoir is transferred to nuclei, thereby enhancing NMR signal intensities. In solid dielectrics there are three mechanisms ... ...

    Abstract Microwave driven dynamic nuclear polarization (DNP) is a process in which the large polarization present in an electron spin reservoir is transferred to nuclei, thereby enhancing NMR signal intensities. In solid dielectrics there are three mechanisms that mediate this transfer--the solid effect (SE), the cross effect (CE), and thermal mixing (TM). Historically these mechanisms have been discussed theoretically using thermodynamic parameters and average spin interactions. However, the SE and the CE can also be modeled quantum mechanically with a system consisting of a small number of spins and the results provide a foundation for the calculations involving TM. In the case of the SE, a single electron-nuclear spin pair is sufficient to explain the polarization mechanism, while the CE requires participation of two electrons and a nuclear spin, and can be used to understand the improved DNP enhancements observed using biradical polarizing agents. Calculations establish the relations among the electron paramagnetic resonance (EPR) and nuclear magnetic resonance (NMR) frequencies and the microwave irradiation frequency that must be satisfied for polarization transfer via the SE or the CE. In particular, if δ, Δ < ω(0I), where δ and Δ are the homogeneous linewidth and inhomogeneous breadth of the EPR spectrum, respectively, we verify that the SE occurs when ω(M) = ω(0S) ± ω(0I), where ω(M), ω(0S) and ω(0I) are, respectively, the microwave, and the EPR and NMR frequencies. Alternatively, when Δ > ω(0I) > δ, the CE dominates the polarization transfer. This two-electron process is optimized when ω(0S(1))-ω(0S(2)) = ω(0I) and ω(M)~ω(0S(1)) or ω(0S(2)), where ω(0S(1)) and ω(0S(2)) are the EPR Larmor frequencies of the two electrons. Using these matching conditions, we calculate the evolution of the density operator from electron Zeeman order to nuclear Zeeman order for both the SE and the CE. The results provide insights into the influence of the microwave irradiation field, the external magnetic field, and the electron-electron and electron-nuclear interactions on DNP enhancements.
    MeSH term(s) Electric Conductivity ; Electron Spin Resonance Spectroscopy/methods ; Electrons ; Magnetic Resonance Spectroscopy/methods ; Microwaves ; Quantum Theory
    Language English
    Publishing date 2011-04-06
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 3113-6
    ISSN 1089-7690 ; 0021-9606
    ISSN (online) 1089-7690
    ISSN 0021-9606
    DOI 10.1063/1.3564920
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Restraints on backbone conformations in solid state NMR studies of uniformly labeled proteins from quantitative amide 15N-15N and carbonyl 13C-13C dipolar recoupling data.

    Hu, Kan-Nian / Qiang, Wei / Bermejo, Guillermo A / Schwieters, Charles D / Tycko, Robert

    Journal of magnetic resonance (San Diego, Calif. : 1997)

    2012  Volume 218, Page(s) 115–127

    Abstract: Recent structural studies of uniformly (15)N, (13)C-labeled proteins by solid state nuclear magnetic resonance (NMR) rely principally on two sources of structural restraints: (i) restraints on backbone conformation from isotropic (15)N and (13)C chemical ...

    Abstract Recent structural studies of uniformly (15)N, (13)C-labeled proteins by solid state nuclear magnetic resonance (NMR) rely principally on two sources of structural restraints: (i) restraints on backbone conformation from isotropic (15)N and (13)C chemical shifts, based on empirical correlations between chemical shifts and backbone torsion angles; (ii) restraints on inter-residue proximities from qualitative measurements of internuclear dipole-dipole couplings, detected as the presence or absence of inter-residue crosspeaks in multidimensional spectra. We show that site-specific dipole-dipole couplings among (15)N-labeled backbone amide sites and among (13)C-labeled backbone carbonyl sites can be measured quantitatively in uniformly-labeled proteins, using dipolar recoupling techniques that we call (15)N-BARE and (13)C-BARE (BAckbone REcoupling), and that the resulting data represent a new source of restraints on backbone conformation. (15)N-BARE and (13)C-BARE data can be incorporated into structural modeling calculations as potential energy surfaces, which are derived from comparisons between experimental (15)N and (13)C signal decay curves, extracted from crosspeak intensities in series of two-dimensional spectra, with numerical simulations of the (15)N-BARE and (13)C-BARE measurements. We demonstrate this approach through experiments on microcrystalline, uniformly (15)N, (13)C-labeled protein GB1. Results for GB1 show that (15)N-BARE and (13)C-BARE restraints are complementary to restraints from chemical shifts and inter-residue crosspeaks, improving both the precision and the accuracy of calculated structures.
    MeSH term(s) Algorithms ; Amides/chemistry ; Bacterial Proteins/chemistry ; Carbon Isotopes ; Computer Simulation ; Crystallization ; Data Interpretation, Statistical ; Escherichia coli/chemistry ; Escherichia coli/genetics ; Magnetic Resonance Spectroscopy/methods ; Models, Molecular ; Nitrogen Isotopes ; Protein Carbonylation ; Protein Conformation ; Proteins/chemistry ; Software
    Chemical Substances Amides ; Bacterial Proteins ; Carbon Isotopes ; Nitrogen Isotopes ; Proteins
    Language English
    Publishing date 2012-03-09
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Intramural
    ZDB-ID 1469665-4
    ISSN 1096-0856 ; 1557-8968 ; 1090-7807 ; 0022-2364
    ISSN (online) 1096-0856 ; 1557-8968
    ISSN 1090-7807 ; 0022-2364
    DOI 10.1016/j.jmr.2012.03.001
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Quantitative determination of site-specific conformational distributions in an unfolded protein by solid-state nuclear magnetic resonance.

    Hu, Kan-Nian / Havlin, Robert H / Yau, Wai-Ming / Tycko, Robert

    Journal of molecular biology

    2009  Volume 392, Issue 4, Page(s) 1055–1073

    Abstract: Solid-state nuclear magnetic resonance (NMR) techniques are used to investigate the structure of the 35-residue villin headpiece subdomain (HP35) in folded, partially denatured, and fully denatured states. Experiments are carried out in frozen glycerol/ ... ...

    Abstract Solid-state nuclear magnetic resonance (NMR) techniques are used to investigate the structure of the 35-residue villin headpiece subdomain (HP35) in folded, partially denatured, and fully denatured states. Experiments are carried out in frozen glycerol/water solutions, with chemical denaturation by guanidine hydrochloride (GdnHCl). Without GdnHCl, two-dimensional solid-state (13)C NMR spectra of samples prepared with uniform (13)C labeling of selected residues show relatively sharp cross-peaks at chemical shifts that are consistent with the known three-helix bundle structure of folded HP35. At high GdnHCl concentrations, most cross-peaks broaden and shift, qualitatively indicating disruption of the folded structure and development of static conformational disorder in the frozen denatured state. Conformational distributions at one residue in each helical segment are probed quantitatively with three solid-state NMR techniques that provide independent constraints on backbone varphi and psi torsion angles in samples with sequential pairs of carbonyl (13)C labels. Without GdnHCl, the combined data are well fit by alpha-helical conformations. At [GdnHCl]=4.5 M, corresponding to the approximate denaturation midpoint, the combined data are well fit by a combination of alpha-helical and partially extended conformations at each site, but with a site-dependent population ratio. At [GdnHCl]=7.0 M, corresponding to the fully denatured state, the combined data are well fit by a combination of partially extended and polyproline II conformations, again with a site-dependent population ratio. Two entirely different models for conformational distributions lead to nearly the same best-fit distributions, demonstrating the robustness of these conclusions. This work represents the first quantitative investigation of site-specific conformational distributions in partially folded and unfolded states of a protein by solid-state NMR.
    MeSH term(s) Amino Acid Sequence ; Computer Simulation ; Freezing ; Microfilament Proteins/analysis ; Microfilament Proteins/chemistry ; Models, Molecular ; Normal Distribution ; Nuclear Magnetic Resonance, Biomolecular/methods ; Peptide Fragments/chemistry ; Protein Denaturation/physiology ; Protein Folding ; Protein Structure, Tertiary/physiology
    Chemical Substances Microfilament Proteins ; Peptide Fragments ; villin
    Language English
    Publishing date 2009-07-30
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Intramural
    ZDB-ID 80229-3
    ISSN 1089-8638 ; 0022-2836
    ISSN (online) 1089-8638
    ISSN 0022-2836
    DOI 10.1016/j.jmb.2009.07.073
    Database MEDical Literature Analysis and Retrieval System OnLINE

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