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Microflex lrf maldi tof ms instrument

Manufactured by Bruker
Sourced in Germany

The Microflex LRF MALDI-TOF MS instrument is a mass spectrometry system that utilizes matrix-assisted laser desorption/ionization (MALDI) and time-of-flight (TOF) mass analysis. It is designed to provide high-performance mass spectrometry capabilities for a variety of applications.

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2 protocols using microflex lrf maldi tof ms instrument

1

MALDI-TOF MS Analysis of Lipid A

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Dried lipid A samples were dissolved with 10 μL of chloroform. Then 1 μL of lipid A sample and 1 μL of 50 mg mL−1 super-DHB (in 70% acetonitrile/water) (Sigma-Aldrich, St. Louis, MO, USA) were loaded onto a MSP 96 target polished steel MALDI plate and dried at room temperature. Lipid A samples were analyzed using Bruker Daltonics Microflex LRF MALDI-TOF MS instrument and FlexControl 3.0 software (Bruker, Bremen, Germany). Operating conditions were as follows: negative-ion and reflectron mode, detector gain = 6.9, laser frequency = 60.0 Hz, and laser power = 87%. MS/MS analysis of lipid A was performed using an Axima Resonance MALDI-quadrupole ion trap-TOF instrument (Shimadzu, Manchester, UK). Fragment ions were analyzed by collision-induced dissociation (CID) of parent ions and argon gas was used as a collision gas. Operating conditions were as follows: negative ion and reflectron mode, intro endcap = −5.5 kV, extr endcap = 10.0 kV, flight tube = 10.0 kV, reflectron center = −0.2 kV, reflectron back = −0.2 kV, detector = 2.2 kV, and laser intensity: 60–100 power. Data acquisition and processing were performed using Launchpad 2.9.3 software (Kratos Analytical, Manchester, UK).
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2

Lipid A Extraction and Analysis by MALDI-TOF MS

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Lipid A analysis was conducted using the methods described in Sorensen et al. (65 (link)). Briefly, pelleted bacteria were smeared onto a MALDI plate with a sterile inoculation loop. A total of 1 μL of buffer, consisting of 0.2 M anhydrous citric acid and 0.1 M trisodium citrate dihydrate, was spotted atop the spotted colony. The plate was then incubated at 110°C for 30 minutes to extract membrane lipids. The plate was then rinsed with endotoxin-free water to wash cell debris. One microliter of 10 mg/mL norharmane matrix suspended in 2:1 chloroform-methanol was spotted onto extracted sample on the MALDI plate. Mass spectra was collected using a Bruker Microflex LRF MALDI-TOF MS instrument in negative ion and reflectron mode.
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