2019
DOI: 10.1016/j.ssnmr.2018.12.003
|View full text |Cite
|
Sign up to set email alerts
|

Hyperpolarized MAS NMR of unfolded and misfolded proteins

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
17
0
1

Year Published

2019
2019
2024
2024

Publication Types

Select...
7
1
1

Relationship

1
8

Authors

Journals

citations
Cited by 26 publications
(18 citation statements)
references
References 119 publications
0
17
0
1
Order By: Relevance
“…S7 (ESI †). 21 Calculating the peak positions using the chemical shift profiles also readily identifies { g m ,t}, { g m ,g m } and {g p ,t} as the major states. Moreover, the populations of the three major states determined from peak volumes in the DQSQ spectrum agree well with those determined in solution from 13 C chemical shifts, in particular a substantial population of { g p ,t}.…”
mentioning
confidence: 99%
“…S7 (ESI †). 21 Calculating the peak positions using the chemical shift profiles also readily identifies { g m ,t}, { g m ,g m } and {g p ,t} as the major states. Moreover, the populations of the three major states determined from peak volumes in the DQSQ spectrum agree well with those determined in solution from 13 C chemical shifts, in particular a substantial population of { g p ,t}.…”
mentioning
confidence: 99%
“…Interessante Anwendungsmöglichkeiten der Festköper-NMR ergeben sich auch mithilfe der dynamischen nuklearen Polarisation (DNP), die zur Signalverstärkung eingesetzt wird. Mittels DNPverstärkter Festköper-NMR-Spektroskopie konnte u. a. experimentell gezeigt werden, dass intrinsisch ungefaltete Proteine bereits im Grundzustand eine Vielzahl unterschiedlicher -teilweise gefalteter -Konformationen durchlaufen [5]. Auch Photointermediate des Rhodopsins konnten kürzlich mittels DNP charakterisiert werden [6].…”
Section: Struktur Und Dynamik Von Membranproteinenunclassified
“…In vitro, there are many studies reporting on the interactions of cyt c with non-CL anionic lipids, including PG, showing the potential for similar interactions to those underpinning CL-induced peroxidase activation [28][29][30][31]. Yet, to the best of our knowledge there is no record of a direct involvement of PG in place of CL in the apoptotic pathway in vivo, with studies showing CL to be the preferred substrate for cyt c binding and peroxidation [2,3,32,33] [34]: the blue foldon (N and C-terminal helices, residues 1-14 and 88-104), the green foldon (helix [61][62][63][64][65][66][67][68][69] and Ω loop [20][21][22][23][24][25][26][27][28][29][30][31][32][33][34][35], the gray foldon (Ω loop [40][41][42][43][44][45][46][47][48][49][50][51]…”
Section: Introductionmentioning
confidence: 99%