Topics in SSNMR and Dynamics of Proteins: Consequences of Intermediate Exchange

Similar documents
Topics in SSNMR and Conformational Dynamics of Biopolymers: Consequences of Intermediate Exchange

Quantification of Dynamics in the Solid-State

Lecture #6 Chemical Exchange

3 Chemical exchange and the McConnell Equations

An introduction to Solid State NMR and its Interactions

NMR Relaxation and Molecular Dynamics

Introduction to Relaxation Theory James Keeler

Effects of Chemical Exchange on NMR Spectra

Cross Polarization 53 53

Heteronuclear Decoupling and Recoupling

The Positive Muon as a Probe in Chemistry. Dr. Iain McKenzie ISIS Neutron and Muon Source STFC Rutherford Appleton Laboratory

Protein dynamics from NMR Relaxation data

Spectral Broadening Mechanisms

NMR in Structural Biology

Structure, dynamics and heterogeneity: solid-state NMR of polymers. Jeremy Titman, School of Chemistry, University of Nottingham

6 NMR Interactions: Zeeman and CSA

NMR: Formalism & Techniques

Spin Dynamics Basics of Nuclear Magnetic Resonance. Malcolm H. Levitt

NMR Dynamics and Relaxation

Advanced Quadrupolar NMR. Sharon Ashbrook School of Chemistry, University of St Andrews

VIII Chemical Exchange

Chemical Shift Anisotropy & Multidimensional Recoupling for Uniformly Labeled Proteins

Effects of Chemical Exchange on NMR Spectra

Physikalische Chemie IV (Magnetische Resonanz) HS Solution Set 2. Hand out: Hand in:

K ex. Conformational equilibrium. equilibrium K B

Slow symmetric exchange

Solid-state NMR and proteins : basic concepts (a pictorial introduction) Barth van Rossum,

Relaxation. Ravinder Reddy

Spin Relaxation and NOEs BCMB/CHEM 8190

T 1, T 2, NOE (reminder)

Biophysical Chemistry: NMR Spectroscopy

Chem8028(1314) - Spin Dynamics: Spin Interactions

Classical Description of NMR Parameters: The Bloch Equations

PROTEIN NMR SPECTROSCOPY

Lecture #7 In Vivo Water

Spin-Boson Model. A simple Open Quantum System. M. Miller F. Tschirsich. Quantum Mechanics on Macroscopic Scales Theory of Condensed Matter July 2012

CHEM / BCMB 4190/6190/8189. Introductory NMR. Lecture 10

Solid-state NMR of spin > 1/2

Classical Description of NMR Parameters: The Bloch Equations

Dipole Recoupling at High Spinning Frequencies. and. High Magnetic Fields

Spectral Broadening Mechanisms. Broadening mechanisms. Lineshape functions. Spectral lifetime broadening

NMR Studies of Polyethylene: Towards the Organization of Semi Crystalline Polymers

NMR Theory and Techniques for Studying Molecular Dynamics

SUPPLEMENTARY NOTE 1: ADDITIONAL CHARACTERIZATION OF NANODIAMOND SOLUTIONS AND THE OVERHAUSER EFFECT

Control of Spin Systems

Principles of Nuclear Magnetic Resonance in One and Two Dimensions

PRACTICAL ASPECTS OF NMR RELAXATION STUDIES OF BIOMOLECULAR DYNAMICS

- Basic understandings: - Mapping interactions:

It is possible to choose the temperature for each experiment by setting a temperature under the Temp pane (under the Standard panel).

Chemical Exchange. Spin-interactions External interactions Magnetic field Bo, RF field B1

Supplementary Figure 1: Spin noise spectra of 55 Mn in bulk sample at BL =10.5 mt, before subtraction of the zero-frequency line. a, Contour plot of

NMR journey. Introduction to solution NMR. Alexandre Bonvin. Topics. Why use NMR...? Bijvoet Center for Biomolecular Research

Muon Spin Relaxation Functions

Timescales of Protein Dynamics

NMR (CHEM8028) Solid-state NMR: Anisotropic interactions and how we use them. Dr Philip Williamson January 2015

Frequency- and Time-Domain Spectroscopy

CONTENTS. 2 CLASSICAL DESCRIPTION 2.1 The resonance phenomenon 2.2 The vector picture for pulse EPR experiments 2.3 Relaxation and the Bloch equations

General NMR basics. Solid State NMR workshop 2011: An introduction to Solid State NMR spectroscopy. # nuclei

H NMR Studies of Molecular Dynamics. Basis Seminar on June 25th by Cornelius Friedrichs

The Physical Basis of the NMR Experiment

Biophysical Chemistry: NMR Spectroscopy

5.74 Introductory Quantum Mechanics II

Model-Free Approach to Internal Motions in Proteins

Timescales of Protein Dynamics

More NMR Relaxation. Longitudinal Relaxation. Transverse Relaxation

Introduction to NMR Product Operators. C. Griesinger. Max Planck Institute for Biophysical Chemistry. Am Faßberg 11. D Göttingen.

4 Spin-echo, Spin-echo Double Resonance (SEDOR) and Rotational-echo Double Resonance (REDOR) applied on polymer blends

Author(s) Takegoshi, K; Nakamura, S; Terao, T.

Theory of double quantum two-dimensional electron spin resonance with application to distance measurements

Muons in Chemistry Training School Dr N J Clayden School of Chemistry University of East Anglia Norwich

MR Fundamentals. 26 October Mitglied der Helmholtz-Gemeinschaft

Longitudinal-relaxation enhanced fast-pulsing techniques: New tools for biomolecular NMR spectroscopy

Magnetic Resonance Imaging. Pål Erik Goa Associate Professor in Medical Imaging Dept. of Physics

Numerical Methods for Pulse Sequence Optimisation

ANALYTICAL AND NUMERICAL INVESTIGATIONS *

Principios Básicos de RMN en sólidos destinado a usuarios. Gustavo Monti. Fa.M.A.F. Universidad Nacional de Córdoba Argentina

Correlation spectroscopy

arxiv:cond-mat/ v1 1 Dec 1999

Principles of Magnetic Resonance Imaging

Chemistry 431. Lecture 23

NUCLEAR MAGNETIC RESONANCE. Introduction. Vol. 10 NUCLEAR MAGNETIC RESONANCE 637

Principles of Magnetic Resonance

Molecular Dynamics and Local Molecular Conformation in Solid Materials Studied by Nuclear Magnetic Resonance

Electron spins in nonmagnetic semiconductors

QENS in the Energy Domain: Backscattering and Time-of

4 DQF-COSY, Relayed-COSY, TOCSY Gerd Gemmecker, 1999

Magnetic resonance in Dense Atomic Hydrogen Gas

TECNICHE DI ALTA E BASSA RISOLUZIONE IN NMR STATO SOLIDO

8 NMR Interactions: Dipolar Coupling

NMR, the vector model and the relaxation

PRACTICAL ASPECTS OF NMR RELAXATION STUDIES OF BIOMOLECULAR DYNAMICS

Site-Resolved Determination of Peptide Torsion Angle O from the Relative Orientations of Backbone N-H and C-H Bonds by Solid-State NMR

Uses of Nuclear Magnetic Resonance (NMR) in Metal Hydrides and Deuterides. Mark S. Conradi

Shimming of a Magnet for Calibration of NMR Probes UW PHYSICS REU 2013

NMR-spectroscopy of proteins in solution. Peter Schmieder

e 2m p c I, (22.1) = g N β p I(I +1), (22.2) = erg/gauss. (22.3)

Protein Dynamics, Allostery and Function

Introduction solution NMR

Renormalization of microscopic Hamiltonians. Renormalization Group without Field Theory

Hyperfine interaction

Transcription:

Topics in SSNMR and Dynamics of Proteins: Consequences of Intermediate Exchange A McDermott, Columbia University Winter School in Biomolecular NMR, Stowe VT January 20-23 2008

Effects on NMR Spectra: Local, Angular Dynamics on Timescales from sec to ps Krushelnitsky & Reichert Prog NMR 2005 1/23/08 2 DHFR Compression: Wright et al, Chem Rev 2006

Notional Regimes for Motion Regime Definition Timescale Consequences Fast τ c << 1/Δω ps-ns Relaxation, reduced apparent tensor breadth Intermediate Exchange τ c 1/Δω τ c > T 2 (or ZQ T 1ρ T 2 etc.) µs Lineshape, 10 7 10 s -1 short coherence times Slow T 1 >τ c >1/Δ ms-sec Population ω exchange Ultraslow τ c > T 1 min- days Time Dep Expts Rate and Amplitude controlled by Temp, Pressure and Hydration 1/23/08 3 A: Def

Chemical Exchange Intermediate Exchange Timescale C 1 k21 k 12 C2 [ K eq = C ] 2 [ C ] = k 12 1 k 21 1/23/08 4

Differential Equation Describing Precession, Chemical Exchange, and Relaxation M 1 t M 2 = iω k R 1 12 2 k 21 M 1 k t 12 iω 2 k 21 R 2 M 2 1/23/08 5 A: Def next

Effect of Precession and Relaxation on Magnetization M 1 t M 2 = iω R 1 2 0 M 1 0 iω t 2 R 2 M 2 M i M x i + im y i M 1 t = ( iω 1 + R 2 )M 1 M i (t) = M i (0)e ( iω i +R 2 )t M(t) = i M i (t) Matrix is diagonal, two separable, solvable equations. 1/23/08 A: Def 6

Effects of Chemical Exchange on Magnetization M 1 t M 2 = k 12 k 21 M 1 k t 12 k 21 M 2 1/23/08 7

Effects of Exchange on Chemical Concentrations C 1 k21 k 12 C 2 C 1 t = k 12 C 1 + k 21 C 2 C 2 t = +k 12 C 1 k 21 C 2 C 1 t C 2 = k 12 k 21 C 1 k t 12 k 21 C 2 1/23/08 8

Solving for Concentration over Time by Matrix Methods v c t = K v c v c = C 1 ;K = k 12 k 21 ; C 2 k 12 k 21 v c (t) = e Kt v c (0) D = U 1 KU K = UDU 1 e Kt = Ue Dt U 1 v c (t) = Ue Dt U 1 v c (0) 1/23/08 9

Ku v v i = λ i u i ; u v i = u i1 D = λ 1 0 0 λ 2 U = K = a c u 11 u 12 u 21 u 22 b d K λi = a λ c λ = a + d 2 ± u i2 b d λ = a λ ( a + d) 2 4( ad bc) 2 Eigenvalue Approach to Diagonalization ( )( d λ) bc = 0 1/23/08 10 A: Meaning of λ

Let s Look at Three Cases λ = a + d ± 2 X = a b = 0 1 c d 1 0 K'= a c K = a c ( a + d) 2 4( ad bc) 2 b d = k k k k b = k 12 k 21 d k 12 k 21 1/23/08 11

Try to Solve a Meaningless Example λ = a + d ± 2 X = a b = 0 1 c d 1 0 λ = 0 ± ( a + d) 2 4( ad bc) ( 0) 2 4( 0 +1) 2 2 = 1 1/23/08 12

Solve the Eigenvalue Problem for Symmetric Two Site Exchange ( a + d) 2 4( ad bc) λ = a + d ± 2 2 K'= a b c d = k k k k λ = 2k 2 ± 2k D = 2k 0 0 0 ( ) 2 4 k 2 k 2 2 ( ) = k ± k 1/23/08 13

Solve for the Transformation Matrices U and U -1 Ku v v i = λ i u i k k u v 1 = 2ku v 1 k k ku 11 ku 12 = 2ku 11 ; ku 11 + ku 12 = 2ku 12 ;u 11 = u 12 k k k u v k 2 = 0k v u 2 ku 21 ku 22 = 0ku 21 ; ku 21 + ku 22 = 0ku 22 ;u 21 = u 22 u U = 11 u 21 = 1 1 u 12 u 22 1 1 U = a c b ;U 1 = 1 d U d c b ;U 1 = 1 1 1 a 2 1 1 1/23/08 14

Homework: Confirm that this expression yields the inverse generally U = a b c d U 1 = 1 U d c b a Homework : Confirm in this specific case that this is the correct transformation matrix K = k k k k U = 1 1 1 1 Homework: Write equations for the concentration over time and check their validity 1/23/08 15

Arbitrary Two-Site Exchange Can Also be Solved ( a + d) 2 4( ad bc) λ = a + d ± 2 2 K = a b = k 12 k 21 c d k 12 k 21 λ = k 12 k 21 2 λ = k ± k k k 12 + k 21 ± ( k 12 k 21 ) 2 4 k 12 k 21 k 12 k 21 2 ( ) See Bernasconi 1976 Relaxation Kinetics Academic Press 1/23/08 16

Note that K is not symmetric; is it always diagonalizable for any dimension? Connected with microscopic reversibility, a similarity transformation (U) symmetrizes K (to form K ), assuring us that it is always diagonalizable. HOMEWORK: Show that if U is defined as below, it renders the matrix of rate constants symmetric. A real symmetric matrix is always diagonalizable. C n k nm = C m k mn U ij = P i δ ij K ' ij = K ij K ji = P j P i K ij 1/23/08 17

Combined Effects of Precession, Chemical Exchange, and Relaxation M 1 t M 2 = iω + k + R 1 2 k M 1 k iω + k + R t 2 M 2 v m (t) = Ue Dt U 1 v m (0) 1/23/08 18

K + R + il = iω + R 2 + k k λ = ( R 2 + k) ± k 2 Ω 2 U = a c b ;U 1 ij = d a = i(ω + Ω 2 k 2 ) 1 ad bc k iω + R 2 + k d c b a b = i(ω Ω 2 k 2 ) c = d = k ( )( d b) M(t) = M 1 (t) + M 2 (t) = a + c ad bc ( )( a c) e λ 1 t + b + d ad bc e λ 2 t 1/23/08 19 A: Meaning of Eigenval, Im vre

Amplitudes in More Detail: Slow Exchange: k<<ω ( )( d b) M(t) = M 1 (t) + M 2 (t) = a + c ad bc λ 1,2 = ( R 2 + k) ± k 2 Ω 2 R 2 + k ± iω a = i(ω + Ω 2 k 2 ) 2iΩ b = i(ω Ω 2 k 2 ) 0 c = d = k ( )( a c) e λ1t + b + d ad bc e λ 2t M(t) = M 1 (t) + M 2 (t) = e λ 1t + e λ 2t = e iωt e (R 2 +k )t + e iωt e (R 2 +k)t S(ω) = k + R 2 ( R 2 + k) 2 + Ω ω ( ) + k + R 2 2 ( R 2 + k) 2 + ( Ω + ω) 2 1/23/08 20 A: Meaning of Ampl Re vs Im

Amplitudes in More Detail: Fast Limit: k>>ω ( )( d b) M(t) = M 1 (t) + M 2 (t) = a + c ad bc λ 1,2 = ( R 2 + k) ± k 2 = ( R 2 + 2k),R 2 a = i(ω + Ω 2 k 2 ) k ( )( a c) e λ1t + b + d ad bc e λ 2t b = i(ω c = d = k Ω 2 k 2 ) k M(t) = M 1 (t) + M 2 (t) 0e λ 1t + 2e λ 2t 2e R 2t S(ω) 2R 2 R 2 2 + ( ω) 2 1/23/08 21

S fast (ω) 2R 2 R 2 2 + ( ω) 2 S slow (ω) = k + R 2 ( R 2 + k) 2 + Ω ω ( ) + k + R 2 2 ( R 2 + k) 2 + ( Ω + ω) 2 1/23/08 22

Triosephosphate Isomerase: Lid Opening~Turnover 1/23/08 23 Sharon Rozovsky et al, JMB 2001

Slow Exchange Limit Contributions to Linewidth K + R + il = iω + R + k 2 k λ = ( R 2 + k) ± k 2 Ω 2 k << Ω λ R 2 + k ± iω k iω + R 2 + k 1/23/08 24

Fast Limit Contributions to Linewidth K + R + il = iω + R + k 2 k λ = ( R 2 + k) ± k 2 Ω 2 k >> Ω λ ( R 2 + 2k), R 2 ( ) x <<1; 1+ x 1+ x 2 +... k iω + R 2 + k λ ( R 2 + 2k), ( R 2 + Ω2 ) 2k 1/23/08 25

Exchange Broadening Interference with Isotropic Chemical Shift Evolution Slow Limit scales with k or 1/τ c Fast Limit scales with 1/k or τ c Maximal effect (coalescence, critical point) when k~δω iso /sqrt(2) to k~δω iso The ability to probe this broadening allows one to study rare events (poorly populated species) 1/23/08 26

Fast Limit Contributions to Linewidth T1ρ, Related to Woessner 1961 J Chem Phys; fast limit R ex = p 1 p 2 ΔΩ 2 /k 1 1+ ω e 2 k 2 CPMG: Allerhand and Gutowsky 1965 J Chem Phys; fast limit approx R ex = 1 2τ ex 1 1 τ CPMG ξ sinh 1 sinh τ CPMGξ τ 2 ex ξ = k 2 4 p 1 p 2 ( ΔΩ) 2 1/23/08 27

Important Alternatives to N-site Hopping Models Smoluchowski equation for continuous diffusion in a potential, U. Potentially more direct connection to molecular interpretation. 1D example below includes diffusion and convection Finite difference numerical approaches used See work of Robert Vold: applications to SSNMR ( ) = D 2 R φ φ + 1 2 kt U' φ ( ) φ + 1 kt U'' ( φ ) 1/23/08 28

Distributed Dynamics P(t)dt = 1 2kΓ(1+1/β) exp( t k β )dt Kaplan and Garroway showed (JMR 1982) that homogeneous and inhomogeneous distributions or rates can be distinguished based on NMR lineshapes. 1/23/08 29

1/23/08 30

Intermediate Exchange Lineshapes H H P( t) dt = 1 k dt 1/23/08 31

Triosephosphate Isomerase Lid Motion Rate ~ Turnover

DNA Dynamics at a Methylation Site [5 -(dgatagcgctatc)-3 ] DNA dodecamer Dynamics Apparent in SSNMR Lineshape Not Seen in Solution NMR Relaxation Miller, Drobny, Varani et al JACS 2006 1/23/08 33

Chemical Exchange During MAS ( ) = ω iso + δ C 1 cos( γ + ω r t) + C 2 cos( 2γ + 2ω r t) + S 1 sin( γ + ω r t) + S 2 cos( 2γ + 2ω r t) ω t [ ] C 1 = 2 sin( 2β) 1+ η cos( 2α ) 2 3 C 2 = 1 2 sin2 β η ( 3 1+ cos2 β)cos 2α S 1 = η 2 3 sin β ( )sin 2α ( ) S 2 = η 3 cos ( β )sin( 2α) ( ) δ η is the tensor width : σ zz - σ iso is the asymmetry : (σ xx - σ yy ) / δ R Z (α)r Y (β)r Z (γ) transforms to the Rotor Fixed Frame at t=0 from the Laboratory Fixed Frame 1/23/08 34

ω t Fast MAS vs. Liquid ( ) = ω iso + δ C 1 cos( γ + ω r t) + C 2 cos( 2γ + 2ω r t) + S 1 sin( γ + ω r t) + S 2 cos( 2γ + 2ω r t) ω r >> δ ( ) ω iso ω t [ ] Simulated using SPINEVOLUTION (Veshtort and Griffin) (Meier and Earl, 1985 JACS; Lyerla Yannoni Fyfe 1982 Acc Chem Res 1/23/08 35

Tensor Orientation Change : Slow MAS 1/23/08 36 See Frydman et al 1990 and Schmidt et al 1986

Tensor Orientation Change : Static See Solum Zilm Michl Grant 1983 1/23/08 37

MAS Lineshapes: Sensitivity to Near Intermediate Exchange Conditions 1/23/08 38 Kristensen et al JMR

Exchange Linewidths f(ω r ) Figure 2 A Schmidt and S Vega J Chem Phys 1987 Linewidths for a system Undergoing 2 site flips: Floquet Treatment vs. Perturbation Approx. R ex δ 2 15 1+ η2 3 τ c 1+ 4ω r 2 τ c 2 ( ) + 2τ ( c 1+ ω 2 2 r τ ) c Suwelack Rothwell and Waugh 80 1/23/08 39

Exchange Linewidths f(ω r ) R ex δ 2 15 for three crystallites 1+ η2 3 τ c 1+ 4ω r 2 τ c 2 ( ) + 2τ ( c 1+ ω 2 2 r τ ) c R ex δ 2 15 9 ( 1+ 3η) 4ω 2 r τ c R ex 3 15 δ 2 1+ η2 τ c 3 1/23/08 40

R ex Linewith Contributions for Interference with Chemical Shift Evolution Slow Limit scales with k or 1/τ c Fast Limit scales with 1/k or τ c Maximal effect (coalescence, critical point) when k~δω iso /sqrt(2) to k~δω iso 1/23/08 41

R ex Linewith Contributions for Interference with Chemical Shift TENSOR Refocusing Slow Limit scales with k or 1/τ c Fast Limit scales with 1/k or τ c Amplitude related to δ/ ω r Maximal effect when k~ω r Effect gone when ω r > δ (or if k is moved out of kinetic regime by heating, cooling, drying etc.) 1/23/08 42

More Generally, This Approach Also Applies to the Density Matrix, With Couplings, etc. v m t = il + R + K ( ) v v ρ = il + R + K t ( ) v ρ m L = [ H,ρ] v ( il(t )+R+K) v ρ (t 0 + t) = e ρ (t 0 ) 1/23/08 43

Interference With Decoupling; Amine Rotor R ex 4ω d 2 I( I +1) 15 τ c 1+ ω 2 2 1 τ c R ex 4ω 2 d I( I +1) τ c 15 R ex 4ω 2 d I( I +1) 15 1 ω 1 2 τ c Rothwell and Waugh 1981 Long et al JACS 1994 1/23/08 44

R ex Linewith Contributions for Interference with Proton Decoupling Slow Limit scales with k or 1/τ c Fast Limit scales with 1/k or τ c Amplitude related to ω D Maximal effect when k~ω 1 Effect gone when ω 1 >>> ω D HH (or if k is moved out of kinetic regime by heating, cooling, drying etc.) 1/23/08 45

R ex -like Interference with Coherent Transfer Assume Coherent Transfer of Longitudinal Magnetization (eg Iz-Sz) involves Intermediary Coherence (eg ZQC) Conformational Exchange Causes Interference with Exchange Mechanism, either because of Failed Decoupling or Fluctuations in Time Dependent Chemical Shift Could be thought of as an exchange broadening on ZQC 1/23/08 46

R ex -like Interference with Coherent Transfer (1) ZQ Coherence experiences fluctuations in dipolar couplings. Dephasing amplitude related to ω D, Maximal effect when k~ω 1 (2) ZQ Coherence experiences chemical shift fluctuations due to changes in orientation of CSA. Dephasing amplitude related to δ, and maximal effect when k~ω r 1/23/08 47

R ex Interference with Coherent Transfer Specific Example which MV set up in SPINEVOLUTION: Two Carbons during RFDR Magnetization Exchange Period Begin with magnetization on one spin only and follow Iz and Sz over time. One of them is also in Chemical Exchange with both CSA (δ= 10 khz) and couplings to attached protons changing. ω r moderate (16 khz). 1/23/08 48

Efficiency of Cross Peak Development in RFDR: Varying the Chemical Exchange Rates 1/23/08 49

Exchange Interference in MAS NMR: dynamics in MAS NMR modulates large anisotropic interactions (1) CSA refocusing under MAS is defeated by large angle jumps if k~ω r and δ~ω r, (2) Decoupling by proton irradiation is defeated by moderate or large angle jumps when k~ω 1 and ω D ~ω 1 (3) The performance of coherent transfer sequences is degraded by large angle jumps over a similar range of conditions (provided transverse coherences are important in the spin evolution). There may be useful analogies between these problems and the wellunderstood effect of exchange induced interference with the evolution of the isotropic shift, and the resultant signature broadening effects (which of course also occurs for MAS NMR). 1/23/08 50

1/23/08 51

Simulate Tensor Orientation Change During MAS (DMS) Conditions as for Schmidt et al, : 108 degree hop, axial static tensor of width 4.6 khz; Simulation with SPINEVOLUTION. Very broad interference condition 1/23/08 52

Tensor Orientation Change : Slow MAS 1/23/08 53 See Frydman et al 1990 and Schmidt et al 1986