Application of Solution nmr spectroscopy to Study Protein Dynamics


Slow Dynamic Interchange between Various Conformations



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2. Slow Dynamic Interchange between Various Conformations 

Processes that occur at timescales much slower than the NMR acquisition time will permit the 

measurements of various states independently. In addition, the measurements from successive 

experiments that track changes within this slow timescale allow the determination of kinetic parameters. 

Hydrogen to deuterium exchange experiments have long been recognized to report on the dynamic 

behavior of a protein backbone [15]. The basic principle is the exchange of the labile protein backbone 

amide group between proton and deuterium from the solvent. This is achieved by the rapid transfer of 

the protonated protein into D

2

O buffer and followed by successive measurements of 



1

H-

15



N-HSQC 

two-dimensional NMR spectra. Intensity changes over time can be translated into a hydrogen 

exchange rate that yields information about the solvent accessibility and local structure stability 

(

i.e.

, hydrogen bonding) that can be influenced by dynamic processes. This type of experiment is also 

often used to study folding events [16,17] where NMR spectroscopy is combined with hydrogen 

exchange pulse labeling, a stopped-flow mixing method to prepare samples with very short exchange 

time [18]. This approach has further led to the development of fast NMR data acquisition methods, 

allowing to record two-dimensional spectra in seconds and the detection of faster exchange rates with 

higher accuracy [19]. 

Different conformers that exchange slower than about one hundred milliseconds, typical of NMR 

data acquisition, will allow the observation of separate NMR signals associated with each conformer 

(Figure 2). Proline 

cis-trans

 isomerization occurs within hundreds of milliseconds because of the 

high-energy barrier between the two possible states. It is typical to find 5% of one population relative 

to the other in protein structures. This equilibrium can be shifted completely towards the low populated 

conformation in some cases. With proper regulation, proline 

cis-trans

 isomerizations can act as 

molecular switches that lead to conversion between two states of different functional relevance [20].  



Entropy

 


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