A new version of the program PARAssign has been evaluated for assignment of NMR resonances of the 76 methyl groups in leucines, isoleucines and valines in a 25Ā*kDa protein, using only the structure of the protein and pseudocontact shifts (PCS) generated with a lanthanoid tag at up to three attachment sites. The number of reliable assignments depends strongly on two factors. The principle axes of the magnetic susceptibility tensors of the paramagnetic centers should not be parallel so as to avoid correlated PCS. Second, the fraction of resonances in the spectrum of a paramagnetic sample that can be paired with the diamagnetic counterparts is critical for the assignment. With the data from two tag positions a reliable assignment could be obtained for 60% of the methyl groups and for many of the remaining resonances the number of possible assignments is limited to two or three. With a single tag, reliable assignments can be obtained for methyl groups with large PCS near the tag. It is concluded that assignment of methyl group resonances by paramagnetic tagging can be particularly useful in combination with some additional data, such as from mutagenesis or NOE-based experiments. Approaches to yield the best assignment results with PCS generating tags are discussed.
[NMR paper] Pseudocontact shifts in biomolecular NMR using paramagnetic metal tags.
Pseudocontact shifts in biomolecular NMR using paramagnetic metal tags.
Related Articles Pseudocontact shifts in biomolecular NMR using paramagnetic metal tags.
Prog Nucl Magn Reson Spectrosc. 2017 Feb;98-99:20-49
Authors: Nitsche C, Otting G
PMID: 28283085
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03-12-2017 12:32 PM
Sequence-specific assignment of methyl groups from the neuronal SNARE complex using lanthanide-induced pseudocontact shifts
Sequence-specific assignment of methyl groups from the neuronal SNARE complex using lanthanide-induced pseudocontact shifts
Abstract
Neurotransmitter release depends critically on the neuronal SNARE complex formed by syntaxin-1, SNAP-25 and synaptobrevin, as well as on other proteins such as Munc18-1, Munc13-1 and synaptotagmin-1. Although three-dimensional structures are available for these components, it is still unclear how they are assembled between the synaptic vesicle and plasma membranes to trigger fast, Ca2+-dependent membrane fusion. Methyl...
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12-18-2016 05:04 AM
Pseudocontact shifts in biomolecular NMR using paramagnetic metal tags
Pseudocontact shifts in biomolecular NMR using paramagnetic metal tags
Publication date: Available online 1 December 2016
Source:Progress in Nuclear Magnetic Resonance Spectroscopy</br>
Author(s): Christoph Nitsche, Gottfried Otting</br>
Graphical abstract
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12-02-2016 07:45 AM
FLAMEnGO 2.0: An Enhanced Fuzzy Logic Algorithm for Structure-Based Assignment of Methyl Group Resonances
FLAMEnGO 2.0: An Enhanced Fuzzy Logic Algorithm for Structure-Based Assignment of Methyl Group Resonances
Publication date: Available online 2 May 2014
Source:Journal of Magnetic Resonance</br>
Author(s): Fa-An Chao , Jonggul Kim , Youlin Xia , Michael Milligan , Nancy Rowe , Gianluigi Veglia</br>
We present an enhanced version of the FLAMEnGO (Fuzzy Logic Assignment of Methyl Group) software, a structure-based method to assign methyl group resonances in large proteins. FLAMEnGO utilizes a fuzzy logic algorithm coupled with Monte Carlo sampling to obtain a...
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05-02-2014 06:49 PM
[NMR paper] Erratum to: PARAssign-paramagnetic NMR assignments of protein nuclei on the basis of pseudocontact shifts.
Erratum to: PARAssign-paramagnetic NMR assignments of protein nuclei on the basis of pseudocontact shifts.
Related Articles Erratum to: PARAssign-paramagnetic NMR assignments of protein nuclei on the basis of pseudocontact shifts.
J Biomol NMR. 2013 Jun 23;
Authors: Skinner SP, Moshev M, Hass MA, Keizers PH, Ubbink M
Abstract
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[NMR paper] PARAssign-paramagnetic NMR assignments of protein nuclei on the basis of pseudocontact shifts.
PARAssign-paramagnetic NMR assignments of protein nuclei on the basis of pseudocontact shifts.
Related Articles PARAssign-paramagnetic NMR assignments of protein nuclei on the basis of pseudocontact shifts.
J Biomol NMR. 2013 Mar 23;
Authors: Skinner SP, Moshev M, Hass MA, Ubbink M
Abstract
The use of paramagnetic NMR data for the refinement of structures of proteins and protein complexes is widespread. However, the power of paramagnetism for protein assignment has not yet been fully exploited. PARAssign is software that uses...
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03-26-2013 01:30 PM
Proteinā??protein HADDocking using exclusively pseudocontact shifts
Proteinā??protein HADDocking using exclusively pseudocontact shifts
<div class="Abstract" lang="en">Abstract <div class="normal">In order to enhance the structure determination process of macromolecular assemblies by NMR, we have implemented long-range pseudocontact shift (PCS) restraints into the data-driven protein docking package HADDOCK. We demonstrate the efficiency of the method on a synthetic, yet realistic case based on the lanthanide-labeled N-terminal Īµ domain of the E. coli DNA polymerase III (Īµ186) in complex with the HOT domain. Docking from the bound form of the two...
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[NMR paper] Improving the accuracy of NMR structures of large proteins using pseudocontact shifts
Improving the accuracy of NMR structures of large proteins using pseudocontact shifts as long-range restraints.
Related Articles Improving the accuracy of NMR structures of large proteins using pseudocontact shifts as long-range restraints.
J Biomol NMR. 2004 Mar;28(3):205-12
Authors: Gaponenko V, Sarma SP, Altieri AS, Horita DA, Li J, Byrd RA
We demonstrate improved accuracy in protein structure determination for large (>/=30 kDa), deuterated proteins (e.g. STAT4(NT)) via the combination of pseudocontact shifts for amide and methyl protons...