Quantitative evaluation of positive ϕ angle propensity in flexible regions of proteins from three-bond J couplings. Issue 8 (29th September 2015)
- Record Type:
- Journal Article
- Title:
- Quantitative evaluation of positive ϕ angle propensity in flexible regions of proteins from three-bond J couplings. Issue 8 (29th September 2015)
- Main Title:
- Quantitative evaluation of positive ϕ angle propensity in flexible regions of proteins from three-bond J couplings
- Authors:
- Lee, Jung Ho
Ying, Jinfa
Bax, Ad - Abstract:
- Abstract : 3 J C′Hα couplings in disordered proteins allow quantitative evaluation of the fraction of time each residue adopts a positive ϕ backbone angle. Abstract : 3 J HNHα and 3 J C′C′ couplings can be readily measured in isotopically enriched proteins and were shown to contain precise information on the backbone torsion angles, ϕ, sampled in disordered regions of proteins. However, quantitative interpretation of these couplings required the population of conformers with positive ϕ angles to be very small. Here, we demonstrate that this restriction can be removed by measurement of 3 J C′Hα values. Even though the functional forms of the 3 J C′Hα and 3 J HNHα Karplus equations are the same, large differences in their coefficients enable accurate determination of the fraction of time that positive ϕ angles are sampled. A four-dimensional triple resonance HACANH[C′] E.COSY experiment is introduced to simultaneously measure 3 J C′Hα and 3 J HNC′ in the typically very congested spectra of disordered proteins. High resolution in these spectra is obtained by non-uniform sampling (in the 0.1–0.5% range). Application to the intrinsically disordered protein α-synuclein shows that while most residues have close-to-zero positive ϕ angle populations, up to 16% positive ϕ population is observed for Asn residues. Positive ϕ angle populations determined with the new approach agree closely with consensus values from protein coil libraries and prior analysis of a large set of other NMRAbstract : 3 J C′Hα couplings in disordered proteins allow quantitative evaluation of the fraction of time each residue adopts a positive ϕ backbone angle. Abstract : 3 J HNHα and 3 J C′C′ couplings can be readily measured in isotopically enriched proteins and were shown to contain precise information on the backbone torsion angles, ϕ, sampled in disordered regions of proteins. However, quantitative interpretation of these couplings required the population of conformers with positive ϕ angles to be very small. Here, we demonstrate that this restriction can be removed by measurement of 3 J C′Hα values. Even though the functional forms of the 3 J C′Hα and 3 J HNHα Karplus equations are the same, large differences in their coefficients enable accurate determination of the fraction of time that positive ϕ angles are sampled. A four-dimensional triple resonance HACANH[C′] E.COSY experiment is introduced to simultaneously measure 3 J C′Hα and 3 J HNC′ in the typically very congested spectra of disordered proteins. High resolution in these spectra is obtained by non-uniform sampling (in the 0.1–0.5% range). Application to the intrinsically disordered protein α-synuclein shows that while most residues have close-to-zero positive ϕ angle populations, up to 16% positive ϕ population is observed for Asn residues. Positive ϕ angle populations determined with the new approach agree closely with consensus values from protein coil libraries and prior analysis of a large set of other NMR parameters. The combination of 3 J HNC′ and 3 J C′C′ provides information about the amplitude of ϕ angle dynamics. … (more)
- Is Part Of:
- Physical chemistry chemical physics. Volume 18:Issue 8(2016)
- Journal:
- Physical chemistry chemical physics
- Issue:
- Volume 18:Issue 8(2016)
- Issue Display:
- Volume 18, Issue 8 (2016)
- Year:
- 2016
- Volume:
- 18
- Issue:
- 8
- Issue Sort Value:
- 2016-0018-0008-0000
- Page Start:
- 5759
- Page End:
- 5770
- Publication Date:
- 2015-09-29
- Subjects:
- Chemistry, Physical and theoretical -- Periodicals
541.3 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cp#!issueid=cp016040&type=current&issnprint=1463-9076 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c5cp04542h ↗
- Languages:
- English
- ISSNs:
- 1463-9076
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6475.306000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 227.xml