Using MUSIC and CC(CO)NH for Backbone Assignment of Two Medium-Sized Proteins Not Fully Accessible to Standard 3D NMR

The backbone assignment of medium-sized proteins is rarely as straightforward as that of small proteins, and thus often requires creative solutions. Here, we describe the application of a combination of standard 3D heteronuclear methods with CC(CO)NH and a variety of MUltiplicity Selective In-phase...

Full description

Bibliographic Details
Main Authors: Annette K. Brenner, Nils Åge Frøystein
Format: Article
Language:English
Published: MDPI AG 2014-06-01
Series:Molecules
Subjects:
Online Access:http://www.mdpi.com/1420-3049/19/7/8890
id doaj-9db01e374d904b70a801990a5fe4a5d5
record_format Article
spelling doaj-9db01e374d904b70a801990a5fe4a5d52020-11-24T21:07:12ZengMDPI AGMolecules1420-30492014-06-011978890890310.3390/molecules19078890molecules19078890Using MUSIC and CC(CO)NH for Backbone Assignment of Two Medium-Sized Proteins Not Fully Accessible to Standard 3D NMRAnnette K. Brenner0Nils Åge Frøystein1Department of Chemistry, University of Bergen, PO Box 7800, 5020 Bergen, NorwayDepartment of Chemistry, University of Bergen, PO Box 7800, 5020 Bergen, NorwayThe backbone assignment of medium-sized proteins is rarely as straightforward as that of small proteins, and thus often requires creative solutions. Here, we describe the application of a combination of standard 3D heteronuclear methods with CC(CO)NH and a variety of MUltiplicity Selective In-phase Coherence transfer (MUSIC) experiments. Both CC(CO)NH and MUSIC are, in theory, very powerful methods for the backbone assignment of proteins. Due to low sensitivity, their use has usually been linked to small proteins only. However, we found that combining CC(CO)NH and MUSIC experiments simplified the assignment of two challenging medium-sized proteins of 13 and 19.5 kDa, respectively. These methods are to some extent complementary to each other: CC(CO)NH acquired with a long isotropic mixing time can identify amino acids with large aliphatic side chains. Whereas the most sensitive MUSIC experiments identify amino acid types that cannot be detected by CC(CO)NH, comprising the residues with acid and amide groups, and aromatic rings in their side chains. Together these methods provide a means of identifying the majority of peaks in the 2D 15N HSQC spectrum which simplifies the backbone assignment work even for proteins, e.g., small kinases, whose standard spectra resulted in little spectral resolution and low signal intensities.http://www.mdpi.com/1420-3049/19/7/8890protein NMR spectroscopybackbone assignmentCC(CO)NHMUSIC
collection DOAJ
language English
format Article
sources DOAJ
author Annette K. Brenner
Nils Åge Frøystein
spellingShingle Annette K. Brenner
Nils Åge Frøystein
Using MUSIC and CC(CO)NH for Backbone Assignment of Two Medium-Sized Proteins Not Fully Accessible to Standard 3D NMR
Molecules
protein NMR spectroscopy
backbone assignment
CC(CO)NH
MUSIC
author_facet Annette K. Brenner
Nils Åge Frøystein
author_sort Annette K. Brenner
title Using MUSIC and CC(CO)NH for Backbone Assignment of Two Medium-Sized Proteins Not Fully Accessible to Standard 3D NMR
title_short Using MUSIC and CC(CO)NH for Backbone Assignment of Two Medium-Sized Proteins Not Fully Accessible to Standard 3D NMR
title_full Using MUSIC and CC(CO)NH for Backbone Assignment of Two Medium-Sized Proteins Not Fully Accessible to Standard 3D NMR
title_fullStr Using MUSIC and CC(CO)NH for Backbone Assignment of Two Medium-Sized Proteins Not Fully Accessible to Standard 3D NMR
title_full_unstemmed Using MUSIC and CC(CO)NH for Backbone Assignment of Two Medium-Sized Proteins Not Fully Accessible to Standard 3D NMR
title_sort using music and cc(co)nh for backbone assignment of two medium-sized proteins not fully accessible to standard 3d nmr
publisher MDPI AG
series Molecules
issn 1420-3049
publishDate 2014-06-01
description The backbone assignment of medium-sized proteins is rarely as straightforward as that of small proteins, and thus often requires creative solutions. Here, we describe the application of a combination of standard 3D heteronuclear methods with CC(CO)NH and a variety of MUltiplicity Selective In-phase Coherence transfer (MUSIC) experiments. Both CC(CO)NH and MUSIC are, in theory, very powerful methods for the backbone assignment of proteins. Due to low sensitivity, their use has usually been linked to small proteins only. However, we found that combining CC(CO)NH and MUSIC experiments simplified the assignment of two challenging medium-sized proteins of 13 and 19.5 kDa, respectively. These methods are to some extent complementary to each other: CC(CO)NH acquired with a long isotropic mixing time can identify amino acids with large aliphatic side chains. Whereas the most sensitive MUSIC experiments identify amino acid types that cannot be detected by CC(CO)NH, comprising the residues with acid and amide groups, and aromatic rings in their side chains. Together these methods provide a means of identifying the majority of peaks in the 2D 15N HSQC spectrum which simplifies the backbone assignment work even for proteins, e.g., small kinases, whose standard spectra resulted in little spectral resolution and low signal intensities.
topic protein NMR spectroscopy
backbone assignment
CC(CO)NH
MUSIC
url http://www.mdpi.com/1420-3049/19/7/8890
work_keys_str_mv AT annettekbrenner usingmusicandccconhforbackboneassignmentoftwomediumsizedproteinsnotfullyaccessibletostandard3dnmr
AT nilsagefrøystein usingmusicandccconhforbackboneassignmentoftwomediumsizedproteinsnotfullyaccessibletostandard3dnmr
_version_ 1716763749239488512