timsTOF Pro 2

 

The Standard for High Speed, High Sensitivity, 4D-Multiomics

 
Today Bruker is pioneering the migration of technology from research to commercial laboratory.
 
The timsTOF Pro 2, powered by the latest parallel accumulation serial fragmentation (PASEF®) technology, paves the way for 4D-Multiomics applications. With its proven robustness, high sensitivity and fast MS/MS acquisition, timsTOF Pro 2 is the platform of choice for 4D-Proteomics, 4D-Metabolomics and 4D-Lipidomics.
timsTOF Pro 2

TIMSTOF PRO 2

A quantum leap in 4D-Omics

Speed

PASEF® technology achieves a >120 Hz sequencing speed without affecting resolution.

Depth

Additional ion mobility dimension increases data completeness.

Robustness

The unique instrument design enables robust performance and routine operation over thousands of samples without requiring cleaning.

Important Features to Consider

The new standard for high speed, high sensitivity 4D-Multiomics

Liquid chromatography (LC) coupled with mass spectrometry (MS) has become the gold standard in various omics fields. However, the coverage of proteomes or metabolomes in complex biological samples remains challenging due to limited speed, sensitivity and resolution of current mass spectrometers.

Adding trapped ion mobility spectrometry (TIMS) to the equation unlocks the parallel accumulation serial fragmentation (PASEF®) acquisition method to provide extremely high MS/MS speed and sensitivity, requiring minimal sample amounts.

Dual-TIMS and CCS-enabled analysis

TIMS is first and foremost a separation technique in the gas phase. This resolves sample complexity through an added dimension of separation in addition to high-performance liquid chromatography (HPLC) and mass spectrometry, increasing peak capacity and confidence in compound characterization.

Equally important, the TIMS device also accumulates and concentrates ions of a given m/z and mobility, enabling a unique increase in sensitivity and speed.

A near 100% duty cycle can be achieved with the dual-TIMS technology facilitating accumulation in the front section, while ions in the rear section are sequentially released depending on their mobility. This process of parallel accumulation serial fragmentation (PASEF®) enables collisional cross section (CCS) analysis.

CCS-enabled analysis opens up many further analytical possibilities, from greater certainty of compound identification to confident library matching and lower false discovery rates (FDRs) in large datasets.

PASEF®

The timsTOF Pro 2 comes with our innovative dual-TIMS analyzer that offers three times higher ion capacity. Simplified ion optics maximize ion transfer and sensitivity to set a new standard in 4D-Multiomics. PASEF® is a redesigned MS/MS technology to meet speed requirements of omics applications. Ions are separated using trapped ion mobility spectrometry, eluted (~ 100 ms) and detected in the quadrupole time of flight (QTOF), generating the TIMS MS heat map.

PASEF® then uses the same TIMS separation to serially fragment ions. The quadrupole isolates a certain ion species during its elution for MS/MS and immediately shifts to the next precursor. Parent and fragment spectra are aligned by mobility values. The timsTOF Pro 2 can achieve a sequencing speed of > 120 Hz in PASEF® mode. Furthermore, the MS/MS spectra quality of low abundant analytes can be enriched by selecting them several times.

Benefits

dia-PASEF® adding confidence to your identifications

Data-independent acquisition (dia)-PASEF® is both more sensitive and selective than traditional DIA approaches as it applies the PASEF® principle to combine the advantages of DIA with the inherent ion efficiency of PASEF®. Over the entire liquid chromatography-mass spectrometry (LC-MS)/MS dia-PASEF® run, a perfect data cuboid is created containing m/z, ion mobility (CCS), retention time and intensity. TIMS separation increases selectivity, excludes singly charged precursors from fragmentation and cleans up the sample by concentrating signals from noise. Making use of the correlation of molecular weight and CCS coded information from the dual-TIMS funnel, dia-PASEF® enables highly confident identification.

Maximize peptide and protein sequence coverage

The robust stainless steel stacked ring ion guide (SRIG) configuration and optimized standard dia-PASEF® methods in timsTOF Pro 2 provides an unprecedented depth of proteome coverage in single shot proteomics. Nearly 9000 protein groups were identified from 200 ng of K562 lysate in 35 minute gradients (~30 sample per day) using a PepSep 25 cm column with nanoElute on a timsTOF Pro 2 and a TIMScore™ powered spectral library.

The timsTOF Pro 2 provides in-depth proteome coverage for everyday cell line proteome quantification experiments directly by database searching and matching between runs without the need for a spectral library. Different database search strategies resulted in very comparable results. PaSER™, enabling real time protein identifications, and MaxQuant resulted in similar ID numbers at both protein and peptide level.

Applications

High-throughput targeted proteomics at unprecedented sensitivity

prm-PASEF® benefits from TIMS as a 4th dimension of separation for unmatched selectivity, the time-focusing of ions in the TIMS cartridge to increase sensitivity, and the high speed facilitated by PASEF® to increase the number of precursor targets. In a single acquisition several hundred precursors can be targeted without compromising the unique selectivity and high sensitivity of the timsTOF Pro 2 instrument.

Combining sensitivity, speed, and selectivity, the prm-PASEF® acquisition method delivered high reproducibility and accurate quantitation for either a high number of targets or for application with short chromatography gradients (i.e. <5 minutes).

Targeted protoemics analysis in a colorectal cancer plasma study. 1565 precursors (Heavy/Light) from 565 proteins were targeted in a prm-PASEF® experiment, using Biognosys’s PQ500 kit.

Expanding the Horizons with 4D-Metabolomics

Non-targeted metabolomics benefits from high MS/MS coverage as a key component of compound annotation. Our optimized 4D-Metabolomics methods provide both quantitative MS profiling data and MS/MS fragmentation spectra in the same sample analysis, achieving majority feature coverage even at low analyte concentrations. PASEF® provides mobility selection prior to fragmentation resulting in clean and unambiguous fragment spectra.

PASEF® is able to mobility select and fragment each compound separately, resulting in clean fragment spectra. Removal of matrix derived MS/MS fragments provides better library matching for Proadifen in MetaboScape® and hence higher confidence in results.

PASEF® improves MS/MS spectra for better library matching results.

Higher confidence with 4D-Lipidomics

Analogous to proteomics samples, lipid extracts have a high sample complexity caused by the structural diversity of lipids. High-quality MS/MS spectra are integral to obtaining confident lipid annotations. PASEF® unlocks CCS-enabled workflows which can be used to additionally boost lipid annotation confidence.

Lipidomics data acquired on a timsTOF Pro 2 can be easily analyzed with MetaboScape®, which features a library-free annotation tool that utilizes published fragmentation rules and novel CCS prediction tools. Make full advantage of all 4 acquired dimensions.

PASEF® can fragment >10x more precursors by using mobility separation. This removes overlapping contaminants and resolves isobaric as well as isomeric lipids. The resulting MS/MS spectra show unique fragments for each lipid class resulting in annotations with increased confidence.

Mobility Offset Mass Aligned (MOMA) data of isobaric lipids (A) Heatmap showing the mobility separation of two isobaric phospholipids co-eluting from reverse phase LC. (B) Clean PASEF® MS/MS spectra after mobility separation. (C) Unique lipid annotations from NIST SRM 1950 (ESI +ve mode) for different gradient run times.

Ultrahigh-throughput confident screening and quantification in complex matrices

The exceptional speed of the timsTOF Pro 2 system allows full unknown screening with either GC-APCI or UHPLC VIP-HESI data acquisition. In combination with TASQ® software, Bruker offers a complete solution from data acquisition to automated data analysis.

Applying mobility-filtering to extracted ion chromatograms increases sensitivity in complex matrices by removing interferences. This can clearly be seen in the trace for Thiacloprid in onion at a concentration of 1 ng/mL. The lower traces have been filtered at progressively narrower mobility ranges, allowing a perfect match to the TargetScreener database, as indicated by the green color of the MRSQC score.

Extremely high robustness

Minimal Cleaning Required

Many MS instruments used for omics applications require monthly cleaning when run 24 hours a day on large sample cohorts. Performance degradation is

noticeable even over shorter time periods. The superior robustness of the timsTOF Pro 2 means that the instrument can be run 24/7 over many weeks without noticeable loss of sensitivity or other performance metrics.

System Components

ionBooster

ionBooster

The ionBooster enhances sensitivity and lowers detection limits by increasing ionization efficiency in a wide range of applications
GC-APCI II

GC-APCI II

Greatest flexibility and highest performance with a combined GC frontend and high-resolution MS system for confident ID of unknown compounds using complementary MS technology
Direct Insertion Probe (DIP)

Direct Insertion Probe (DIP)

Direct analysis of liquid and solid samples without tedious sample preparation. Add-on for the Bruker APCI II and APPI II ion sources.
APPI II

APPI II

APPI is used for less polar or non-polar molecules that can not be ionized in either ESI or APCI.
APCI II

APCI II

Used for less polar molecules where ESI fails to deliver reasonable quantities of ions
VIP-HESI dual source

VIP-HESI dual source

Next generation in Mass Spectrometry sensitivity
CaptiveSpray Ion Source

CaptiveSpray Ion Source

Stable and robust nanoflow LC/MS

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