| Literature DB >> 31951864 |
Alia Hassan1, Caitlin M Quinn2, Jochem Struppe3, Ivan V Sergeyev3, Chunting Zhang2, Changmiao Guo2, Brent Runge4, Theint Theint5, Hanh H Dao5, Christopher P Jaroniec5, Mélanie Berbon6, Alons Lends6, Birgit Habenstein6, Antoine Loquet6, Rainer Kuemmerle7, Barbara Perrone8, Angela M Gronenborn9, Tatyana Polenova10.
Abstract
Despite breakthroughs in MAS NMR hardware and experimental methodologies, sensitivity remains a major challenge for large and complex biological systems. Here, we report that 3-4 fold higher sensitivities can be obtained in heteronuclear-detected experiments, using a novel HCN CPMAS probe, where the sample coil and the electronics operate at cryogenic temperatures, while the sample is maintained at ambient temperatures (BioSolids CryoProbe™). Such intensity enhancements permit recording 2D and 3D experiments that are otherwise time-prohibitive, such as 2D 15N-15N proton-driven spin diffusion and 15N-13C double cross polarization to natural abundance carbon experiments. The benefits of CPMAS CryoProbe-based experiments are illustrated for assemblies of kinesin Kif5b with microtubules, HIV-1 capsid protein assemblies, and fibrils of human Y145Stop and fungal HET-s prion proteins - demanding systems for conventional MAS solid-state NMR and excellent reference systems in terms of spectral quality. We envision that this probe technology will be beneficial for a wide range of applications, especially for biological systems suffering from low intrinsic sensitivity and at physiological temperatures.Entities:
Keywords: Biological assemblies; CryoProbe; MAS NMR; Magic angle spinning
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Year: 2019 PMID: 31951864 PMCID: PMC7060763 DOI: 10.1016/j.jmr.2019.106680
Source DB: PubMed Journal: J Magn Reson ISSN: 1090-7807 Impact factor: 2.229