Market leading innovations with the latest in Bruker’s QTOF technology, already proven on impact series. Ultra High Time-of-Flight resolution across wide m/z. Bruker Corporation – maXis impactmaximum speed – definitive answers, Until now, mass spectrometry technologies have forced scientists to choose between. Analysis of a tryptic digest of a human tumor cell line HT29 was performed using a Bruker maXis impact™ high resolution QTOF mass spectrometer. One µg of.

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The latter allow a mass resolution and mass accuracy that is compatible with the high demands of shotgun proteomics of complex mixtures. After stringent filtering Experimental Procedures we performed a principal component analysis PCA to evaluate the similarities and dissimilarities of the cell lines on a global scale.

Together, such advances are making shotgun proteomics increasingly comprehensive and deep analyses can now be performed in a reasonable time 1317 — This QTOF instrument is a member of an instrument family first introduced inwhich consists of the compact, the impact, and the maXis.

maXis II from Bruker Daltonics | SelectScience

Published online May Abstract Hybrid quadrupole time-of-flight QTOF mass spectrometry is one of the two major principles used in proteomics. Advanced Reviewer Member since: This is to our knowledge the deepest proteome coverage of a human cell line measured with a QTOF instrument.

Here we developed MaxQuant further in order to analyze QTOF data and also in this context profit from the high mass accuracy provided by nonlinear mass recalibration algorithms.

Reviewer Membership Status SelectScience Members can achieve membership status by writing product reviews. The Bruker impact platform hruker QTOF instruments takes advantage of these developments and here we maxia and evaluate the impact II for shotgun proteomics applications.


Analysis of the yeast samples were based on label-free intensities LFQ values. In each run MaxQuant identified on average 35, unique peptide sequences, which results in total of 48, unique peptide sequences in the triplicate analysis Table I.

Improvements to the MCP detector include an kaxis entrance aperture, higher electron accelerating fields and optimized shielding. There is a hexapole ion guide between funnel and the analytical quadrupole mass filter, which has a monolithic design based on high precision glass. Spectra with and without transfer time stepping, reveal the beneficial effect on low mass ions without appreciable loss in the standard mass range Fig.

Fundamental challenges of shotgun proteomics include the very large numbers of peptides that elute over relatively short periods and peptide abundances that vary by many orders bruked magnitude. Supplementary Material Supplemental Data: In concordance with others 2627we conclude that the improvements in QTOF technologies in recent years now clearly enable demanding, in-depth analysis of brukdr complex proteomes. MaxQuant employs a double search strategy, in effect supplying hundreds of reference masses internal to each proteomic sample.

IonBench with the Bruker MAXIS IMPACT HD mass spectrometer.

In total, we identified 11, proteins from a single analysis of 24 fractions 2 days of measurement bruer Fig. More than proteins can be identified in a single run of HeLa digest in a 90 min gradient. Triplicate analysis of HeLa and yeast digest using a 90 min gradient for single shot analysis. After a further digestion with trypsin ratio 1: For the principal component analysis PCA of the different cell lines, we furthermore limited the data set LFQ intensities to entries with a minimum of four valid values in at least one group of six replicates.

ACumulative number of identified peptides of triplicate analysis of HeLa. The service from Bruker bduker always been prompt and professional. Secure We only pass your details on to trusted suppliers at your request. In practice, however, the extraction time from the collision cell toward the gate lens is a function of ion mobility. Proteins marked in red are significantly more abundant in haploid cells.


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With resolution 80k and mass accuracy ” Review date: BQuantitative differences between the haploid naxis diploid yeast proteome. Dynamic exclusion duration was 0.

Briefly, ions are produced in the CaptiveSpray, which is in an encased nanoelectrospray source that features a well-defined gas stream to guide the ions into the vacuum via a capillary inlet.

This feature efficiently removes any effect of the temperature related mass drift.

Predigested yeast sample Promega was re-suspended in 0. S1 to S4 and Tables S1 and S2. This helps other members to better understand the Reviewer’s experience and expertise. As in our previous large-scale analysis on SILAC labeled haploid and diploid yeast 50we found transposons more abundant in haploid cells than in diploid cells Fig.

The maXis Impact™ Mass Spectrometer Identifies >1600 Proteins In A Single LC-MS/MS Experiment

Wide dynamic range at high speed is a prerequisite for high-resolution detection of low-abundance compounds in sharp UHPLC peaks and permits direct quantitation without re-run. Cell lysates were diluted 1: Furthermore, we wished to incorporate a column oven and pulled tip columns. Using the axial field gradient results in comparable ion density at the collision cell exit in much shorter time than without, i.