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使用PARAssign通过赝接触位移进行甲基基团归属

Methyl group assignment using pseudocontact shifts with PARAssign.

作者信息

Lescanne Mathilde, Skinner Simon P, Blok Anneloes, Timmer Monika, Cerofolini Linda, Fragai Marco, Luchinat Claudio, Ubbink Marcellus

机构信息

Leiden Institute of Chemistry, Leiden University, Einsteinweg 55, 2333 CC, Leiden, The Netherlands.

Department of Molecular and Cell Biology, Leicester Institute for Structural- and Chemical Biology, University of Leicester, Lancaster Road, Leicester, LE1 7RH, UK.

出版信息

J Biomol NMR. 2017 Dec;69(4):183-195. doi: 10.1007/s10858-017-0136-3. Epub 2017 Nov 27.

Abstract

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 25 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.

摘要

已对程序PARAssign的新版本进行了评估,该版本用于在仅使用蛋白质结构和在多达三个附着位点带有镧系标签产生的伪接触位移(PCS)的情况下,对一个25 kDa蛋白质中亮氨酸、异亮氨酸和缬氨酸的76个甲基的NMR共振进行归属。可靠归属的数量在很大程度上取决于两个因素。顺磁中心的磁化率张量的主轴不应平行,以避免PCS相关。其次,顺磁样品光谱中可与抗磁对应物配对的共振分数对于归属至关重要。利用来自两个标签位置的数据,可以对60%的甲基进行可靠归属,对于许多其余的共振,可能的归属数量限制为两个或三个。使用单个标签时,可以对标签附近具有大PCS的甲基进行可靠归属。得出的结论是,通过顺磁标记对甲基共振进行归属,与一些额外数据(如来自诱变或基于NOE的实验的数据)相结合可能特别有用。讨论了使用产生PCS的标签获得最佳归属结果的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee10/5736784/8e01bf245957/10858_2017_136_Fig1_HTML.jpg

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本文引用的文献

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2
Sequence-specific assignment of methyl groups from the neuronal SNARE complex using lanthanide-induced pseudocontact shifts.
J Biomol NMR. 2016 Dec;66(4):281-293. doi: 10.1007/s10858-016-0078-1. Epub 2016 Dec 17.
3
Isotope-labeling strategies for solution NMR studies of macromolecular assemblies.
Curr Opin Struct Biol. 2016 Jun;38:75-82. doi: 10.1016/j.sbi.2016.05.008. Epub 2016 Jun 10.
4
Highly efficient residue-selective labeling with isotope-labeled Ile, Leu, and Val using a new auxotrophic E. coli strain.
J Biomol NMR. 2016 Jun;65(2):109-19. doi: 10.1007/s10858-016-0042-0. Epub 2016 Jun 6.
5
Review: The HSP90 molecular chaperone-an enigmatic ATPase.
Biopolymers. 2016 Aug;105(8):594-607. doi: 10.1002/bip.22835.
6
Methyl groups as NMR probes for biomolecular interactions.
Curr Opin Struct Biol. 2015 Dec;35:60-7. doi: 10.1016/j.sbi.2015.08.010. Epub 2015 Nov 9.
7
FLAMEnGO 2.0: an enhanced fuzzy logic algorithm for structure-based assignment of methyl group resonances.
J Magn Reson. 2014 Aug;245:17-23. doi: 10.1016/j.jmr.2014.04.012. Epub 2014 May 2.
9
PARAssign--paramagnetic NMR assignments of protein nuclei on the basis of pseudocontact shifts.
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10
MAP-XSII: an improved program for the automatic assignment of methyl resonances in large proteins.
J Biomol NMR. 2013 Feb;55(2):179-87. doi: 10.1007/s10858-012-9700-z. Epub 2013 Jan 5.

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