[NMR paper] Spin Saturation Transfer Difference NMR (SSTD NMR): A New Tool to Obtain Kinetic Parameters of Chemical Exchange Processes.
Spin Saturation Transfer Difference NMR (SSTD NMR): A New Tool to Obtain Kinetic Parameters of Chemical Exchange Processes.
Spin Saturation Transfer Difference NMR (SSTD NMR): A New Tool to Obtain Kinetic Parameters of Chemical Exchange Processes.
J Vis Exp. 2016 Nov 12;(117):
Authors: Quirós MT, Macdonald C, Angulo J, Muñoz MP
Abstract
This detailed protocol describes the new Spin Saturation Transfer Difference Nuclear Magnetic Resonance protocol (SSTD NMR), recently developed in our group to study processes of mutual-site...
nmrlearner
Journal club
0
12-04-2016 02:24 AM
[NMR paper] Transfer Rate Edited Experiment for the Selective Detection of Chemical Exchange via Saturaion Transfer (TRE-CEST)
Transfer Rate Edited Experiment for the Selective Detection of Chemical Exchange via Saturaion Transfer (TRE-CEST)
Publication date: Available online 7 May 2015
Source:Journal of Magnetic Resonance</br>
Author(s): Joshua I. Friedman , Ding Xia , Ravinder R. Regatte , Alexej Jerschow</br>
Chemical Exchange Saturation Transfer (CEST) magnetic resonance experiments have become valuable tools in magnetic resonance for the detection of low concentration solutes with far greater sensitivity than direct detection methods. Accurate measures of rates of chemical exchange...
[Question from NMRWiki Q&A forum] Saturation transfer difference TROSY
Saturation transfer difference TROSY
Has anyone added a pulse scheme for cross saturation to their TROSY for Bruker platform?
Could you share a pulse sequence if you have one?
Thanks!
nmrlearner
News from other NMR forums
0
05-18-2013 09:22 AM
NMR as a tool to identify and characterize protein folding intermediates
NMR as a tool to identify and characterize protein folding intermediates
Available online 12 September 2012
Publication year: 2012
Source:Archives of Biochemistry and Biophysics</br>
</br>
NMR spectroscopy is one of the few biophysical methods that can provide atomic-level insight into the conformation of partially folded states and/or intermediates present along the protein folding pathway. Such studies are important not only within the context of the protein folding problem, but also to push forward the technique, due to the challenging nature of the systems studied....
nmrlearner
Journal club
0
02-03-2013 10:13 AM
[Question from NMRWiki Q&A forum] Can anyone help me with Saturation Transfer NMR
Can anyone help me with Saturation Transfer NMR
Hi I am working on a Varian 500MHz NMR. I am attempting to use the pulse sequence satxfer1D to measure the rate constant of an exchanging system. I am not using solvent suppression and I am having trouble understanding the physics behind the "mixing time" after the 90 pulse. I also do not know how many iterations the selective pulse should go through because it seems that if I turn the mixing time off and just use a selective pulse, and then a pw90, I will still obtain the same spectrum no matter how many iterations the selective pulse train...
nmrlearner
News from other NMR forums
0
09-29-2011 07:36 PM
[U. of Ottawa NMR Facility Blog] Saturation Transfer and Exchange
Saturation Transfer and Exchange
Exchange processes that occur on the NMR time scale affect the NMR line shapes and can be studied by line shape analysis. If the exchange process is slow on the NMR time scale, one can employ EXSY or inversion transfer methods to study the exchange. An alternative to these is the saturation transfer technique. In this method, one of the slowly exchanging resonances (A) is saturated with low power CW irradiation and the effect on the intensity of the resonance of the exchange partner (B) is monitored. If there is exchange between A and B during the period of...
nmrlearner
News from NMR blogs
0
08-03-2011 01:00 AM
[Question from NMRWiki Q&A forum] saturation transfer method in NMR
saturation transfer method in NMR
What is meant by saturation transfer method in NMR? How it is useful in giving the structure of blue copper proteins like Azurin, Plastocyanin and Stellacyani? What is the need to go for this technique in blue copper proteins?
Check if somebody has answered this question on NMRWiki QA forum