Literature DB >> 34759382

Label-free cell assays to determine compound uptake or drug action using MALDI-TOF mass spectrometry.

Melissa S Unger1, Martina Blank1,2, Thomas Enzlein1, Carsten Hopf3.   

Abstract

Cell-based assays for compound screening and profiling are fundamentally important in life sciences, chemical biology and pharmaceutical research. Most cell assays measure the amount of a single reporter molecule or cellular endpoint, and require the use of fluorescence or other labeled materials. Consequently, there is high demand for label-free technologies that enable multiple biomolecules or endpoints to be measured simultaneously. Here, we describe how to develop, optimize and validate MALDI-TOF mass spectrometry (MS) cell assays that can be used to measure cellular uptake of transporter substrates, to monitor cellular drug target engagement or to discover cellular drug-response markers. In uptake assays, intracellular accumulation of a transporter substrate and its inhibition by test compounds is measured. In drug response assays, changes to multiple cellular metabolites or to abundant posttranslational protein modifications are monitored as reporters of drug activity. We detail a ten-part optimization protocol with every part taking 1-2 d that leads to a final 2 d optimized procedure, which includes cell treatment, transfer, MALDI MS-specific sample preparation, quantification using stable-isotope-labeled standards, MALDI-TOF MS data acquisition, data processing and analysis. Key considerations for validation and automation of MALDI-TOF MS cell assays are outlined. Overall, label-free MS cell-based assays offer speed, sensitivity, accuracy and versatility in drug research.
© 2021. The Author(s), under exclusive licence to Springer Nature Limited.

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Year:  2021        PMID: 34759382     DOI: 10.1038/s41596-021-00624-z

Source DB:  PubMed          Journal:  Nat Protoc        ISSN: 1750-2799            Impact factor:   13.491


  6 in total

Review 1.  Cigarette smoking. Health effects and cessation strategies.

Authors:  D P Sachs
Journal:  Clin Geriatr Med       Date:  1986-05       Impact factor: 3.076

2.  [Blood pressure readings in a healthy population].

Authors:  A Jacobowicz; G Zikel
Journal:  Dapim Refuiim       Date:  1965-08

3.  Catecholamine distribution in mice afflicted with muscular dystrophy.

Authors:  P Gordon; R M Dowben
Journal:  Am J Physiol       Date:  1966-04

4.  Traumatic brain syndrome. Psychological sequelae in a case undergoing remission.

Authors:  W T Luckey
Journal:  Minn Med       Date:  1967-11

5.  Control of hepatic and intestinal blood flow: effect of isovolaemic haemodilution on blood flow and oxygen uptake in the intact liver and intestines.

Authors:  W W Lautt
Journal:  J Physiol       Date:  1977-02       Impact factor: 5.182

6.  Bronchodilator response in chronic obstructive pulmonary disease.

Authors:  N R Anthonisen; E C Wright
Journal:  Am Rev Respir Dis       Date:  1986-05
  6 in total
  2 in total

1.  Identification of RNA Fragments Resulting from Enzymatic Degradation using MALDI-TOF Mass Spectrometry.

Authors:  Shawn W Schowe; Conner J Langeberg; Erich G Chapman; Kitty Brown; Marino J E Resendiz
Journal:  J Vis Exp       Date:  2022-04-11       Impact factor: 1.424

2.  LPS-induced lipid alterations in microglia revealed by MALDI mass spectrometry-based cell fingerprinting in neuroinflammation studies.

Authors:  Martina Blank; Thomas Enzlein; Carsten Hopf
Journal:  Sci Rep       Date:  2022-02-21       Impact factor: 4.379

  2 in total

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