While being extremely versatile, NMR has the inherent challenge of being insensitive. One strategy to improve the signal-to-noise ratio is to cryogenically cool the RF components of the NMR probe. The resulting reduced level of thermal noise generated by the RF coil, the network, and the preamplifiers leads to a significant boost in sensitivity while maintaining the sample in its original composition. While the RF components of the probe are cooled to cryogenic temperatures, the temperature of the sample can be controlled independently and kept close to room temperature to preserve the sample’s natural line width.
Bruker’s CPMAS CryoProbes are available in two RF configurations, with one geared towards biological research (HCN) and the other towards material research (HX). CPMAS CryoProbes are available for a range of different frequencies.
Bruker’s CPMAS CryoProbes are compatible with standard bore magnets. Cryogenic cooling is provided by Bruker’s proven CryoPlatform. The probe reaches magic angle spinning rates of 20 kHz with special, volume-optimized 3.2 mm rotors. A fully motorized probe lift is used to move the CPMAS CryoProbe in and out of the magnet for easy and convenient sample changes. For such sample changes, the probe can remain cold. Automatic tuning and matching add to the probe’s ease of use.
The BioSolids CryoProbe allows to study challenging biological systems under physiological temperatures and without altering their sample composition.
This feature is extremely important in structural biology, as the integrity and temperature of the protein surrounding, are often crucial to maintain the biological function.
Diluted samples, such as labelled proteins in their native environment or small molecules in large assemblies, and samples in natural abundance or with low level of labelling, greatly benefit from the significant boost in sensitivity of this innovative probe.
In the pharmacological context, this probe allows to expand the NMR toolbox. 2D ¹³C¹³C correlation experiments can be routinely used for advanced characterization of active pharmaceutical ingredients in natural abundance. Other fields of applications include drug polymorphism and drug-delivery systems
Faster Data Acquisition
Amyloid fibrils and Prions
~ 96.7 mg (u- ¹³C, ¹⁵N) HET-s (218-289) prion domain, courtesy of prof. A.Loquet, CNRS, Bordeaux, France.
Thanks to the enhanced sensitivity the spectra are recorded one order of magnitude faster and it’s possible to record the spectra with just a single scan and with an amazing signal-to-noise and resolution.
Faster Data Acquisition
Amyloid fibrils and Prions
~ 96.7 mg (u- ¹³C, ¹⁵N) HET-s (218-289) prion domain, courtesy of prof. A.Loquet, CNRS Bordeaux, France.
Thanks to the enhanced sensitivity the spectra are recorded one order of magnitude faster and it’s possible to record the spectra with just a single scan and with an amazing signal-to-noise and resolution.
This results into a large time saving for the setup and acquisition of multidimensional experiments.
Gain One Dimension
Amyloid fibrils and Prions
~ 96.7 mg (u- 13C, 15N) HET-s (218-289) prion domain, courtesy of prof. A.Loquet, CNRS Bordeaux, France.
With the sensitivity provided by the BioSoldis CryoProbe the number of scans can be drastically reduced. As a consequence, the multidimensional experiments become faster. It is then possible to perform a 3D experiment in the same time normally required to run a 2D experiment. Also 4D experiments, routinely not performed because of too long acquisition time, become accessible, requiring less than a week of experimental time.
Explore Low Sensitivity Samples
Large biological assemblies
~ 7.5 mg of U – ¹³C, ¹⁵N – labeled Kif5b, a 349-residue protein, complexed with microtubules. Total sample amount ~ 80 mg, courtesy of prof. T.Pollenova, U.Delaware, USA.
Thanks to the sensitivity enhancement more challenging samples, more complex or less labeled, become the focus of the researcher.
We have recorded 3D NCACX and NCOCX experiments have been recorded on sample constituted of a labelled protein of about 350 residues in a complex with an unlabelled protein (total The total amount of isotopically labeled material is ~9 %).
These experiments, which lasted for ~5 and 6 day respectively, demonstrate the stability of the probe over several days of accumulation under multiple steps of simultaneous irradiation on all RF channels.
Biological Samples in their Native Environment
Bacteria cell envelope of mycobacteria
~ 40 mg ¹³C, ¹⁵N-labeled cell wall, HEPES 50 mM pH 7.0, courtesy of prof. J.P.Simorre, U.Grenoble, France.
Thanks to the sensitivity enhancement, the researchers can look with solid state NMR directly into cells.
This probe is a game changer for unstable samples that tends to degrade fast over time. On these kind of samples is crucial to be able to collect all the data shortly after they production.
Natural Products at Natural Abundance
Wood and Cellulose
Wood from Bordeaux wine threes, courtesy of prof. A.Loquet, CNRS Bordeaux, France.
Wood and other cellulose-rich samples typically present a mixture of amorphous and crystalline materials, and therefore a mixture of large and narrow signals. Distinguish between the different overlapping spectral components in a ¹D ¹³C experiment is often not easy. Being able to improve the resolution with a ²D CC correlation experiment is sometimes the only viable way to assign the spectral components. With the improved sensitivity of the BioSolids CryoProbe a refocused INADEQUATE become a routine tool.
Natural Products at Natural Abundance
Native collagen inside bone matrix
Cortical femora bone of Goat (Capra hircus, 2-3 years old). N.Sinha, Centre of Biomedical Research, India.
Understanding the structural and functional behaviour of collagen in its true native state in healthy and diseased conditions is a milestone for the development of treatments for various bone degenerative diseases, tissue engineering, and bone implants. Natural abundance spectra of collagen typically suffer of low sensitivity and limited isotopic concentration.
Thanks to sensitivity enhancement of this probe, it is now possible to record high-resolution 2D ¹H-¹³C HETCOR experiments of collagen in natural isotopic abundance. The spectra, recorded at short and long contact times , shed light on short and long-range interactions of collagen inside the bone matrix in its true native environments. With this probe, the researchers go one step further in the understanding of the structural stability and functional mechanism of collagen inside the bone matrix.
In-situ Characterization of Active Pharmaceutical Ingredients
Cyclodextrin-based metal-organic frameworks (CD-MOFs)
CDMOFs particles loaded with ~ 20 % Lansoprazole, courtesy of prof. C.Martineau-Corcos, CEMHTI UPR CNRS 3079, ILV UMR CNRS 8180, and IUF, France.
Drug-delivery matrixes are often porous materials which resemble sponges. Metal-organic frameworks (CD-MOFs) are good example, as they are materials with a huge empty volume. Drugs loaded into MOFs represent a case of diluted spin systems, in which the sensitivity lack represent a big issue for the in-situ characterization of the active ingredient.
It is worth to note that the cryoprobe technology is so far the only tool that allows probing the state of a low API content in these kind of samples. Other approaches, like fast MAS 1H NMR or DNP have been demonstrated to be not suitable or of limited use, because of lack of resolution and unstability of CD-MOFs in the solvents used for DNP sample preparation.
Thanks to the superior sensitivity of the probe, advanced characterization of an API can be performed without resorting to isotopic labeling. This is illustrated with a CC double quantum correlation on vitamin B12 at natural abundance. The refocused INADEQUATE has notoriously low sensitivity, and it would have taken more than one month acquisition time on a RT probe.
The CPMAS CryoProbe is developed for standard and advanced CP-based experiments in structural biology.
The high sensitivity of the new probe in combination with Non-Uniform Sampling techniques enables a dramatic reduction of experiment times. The CPMAS CryoProbe allows up to 10 times faster data acquisition for sensitivity limited samples.
1.NPM1 exhibits structural and dynamic heterogeneity upon phase separation with the p14ARF tumor suppressor
Eric Gibbs, Barbara Perrone, Alia Hassan, Rainer Kümmerle, Richard Kriwacki.
Journal of Magnetic Resonance, 2020, 310, 10646
2.Sensitivity Boosts by the CPMAS CryoProbe for Challenging Biological Assemblies
Alia Hassan, Caitlin M.Quinn, Jochem Struppe, Ivan V.Sergeyev, Chunting Zhang, Changmiao Guo, Brent Runge, Theint Theint, Hanh H.Dao, Christopher P. Jaroniec, Mélanie Berbon, Alons Lends, Birgit Habenstein, Antoine Loquet, Rainer Kuemmerle, Barbara Perrone, Angela Gronenborn, Tatyana Polenova.
Journal of Magnetic Resonance, 2020, 311, 106680
3.Efficient incorporation and protection of lansoprazole in cyclodextrin metal-organic frameworks
Xue Li, Marianna Porcino, Charlotte Martineau Corcos, Tao Guo, Ting Xiong, Weifen Zhu, Gilles Patriarch, Christine Péchoux, Barbara Perrone, Alia Hassan, Rainer Kümmerle, Alexandre Michelet, Anne Zehnacker-Rentien, Jiwen Zhang Ruxandra Gref.
International Journal of Pharmaceutics, 2020, 585, 119442
4.Probing short and long-range interactions in native collagen inside the bone matrix by BioSolids CryoProbe
Nidhi Tiwari, Sebastian Wegner, Alia Hassan, Navneet Dwivedi, RamaNand Rai, and Neeraj Sinha.
Accepted in Magnetic Resonance in Chemistry