scholarly journals The Value of Activated Ion Electron Transfer Dissociation for High-Throughput Top-Down Characterization of Intact Proteins

2018 ◽  
Vol 90 (14) ◽  
pp. 8553-8560 ◽  
Author(s):  
Nicholas M. Riley ◽  
Jacek W. Sikora ◽  
Henrique S. Seckler ◽  
Joseph B. Greer ◽  
Ryan T. Fellers ◽  
...  
2018 ◽  
Vol 90 (15) ◽  
pp. 8946-8953 ◽  
Author(s):  
Matthew J. P. Rush ◽  
Nicholas M. Riley ◽  
Michael S. Westphall ◽  
Joshua J. Coon

2013 ◽  
Vol 11 (1) ◽  
pp. 25-34 ◽  
Author(s):  
Corina Flangea ◽  
Catalin Schiopu ◽  
Florina Capitan ◽  
Cristina Mosoarca ◽  
Marilena Manea ◽  
...  

AbstractThe conventional protocol for protein identification by electrospray ionization mass spectrometry (MS) is based on enzymatic digestion which renders peptides to be analyzed by liquid chromatography-MS and collision-induced dissociation (CID) multistage MS, in the so-called bottom-up approach. Though this method has brought a significant progress to the field, many limitations, among which, the low throughput and impossibility to characterize in detail posttranslational modifications in terms of site(s) and structure, were reported. Therefore, the research is presently focused on the development of procedures for efficient top-down fragmentation of intact protein ions. In this context, we developed here an approach combining fully automated chip-based-nanoelectrospray ionisation (nanoESI), performed on a NanoMate robot, with electron transfer dissociation (ETD) for peptide and top-down protein sequencing and identification. This advanced analytical platform, integrating robotics, microfluidics technology, ETD and alternate ETD/CID, was tested and found ideally suitable for structural investigation of peptides and modified/functionalized peptides as well as for top-down analysis of medium size proteins by tandem MS experiments of significantly increased throughput and sensitivity. The obtained results indicate that NanoMate-ETD and ETD/CID may represent a viable alternative to the current MS strategies, with potential to develop into a method of routine use for high throughput top-down proteomics.


2020 ◽  
Vol 92 (15) ◽  
pp. 10246-10251 ◽  
Author(s):  
Jean M. Lodge ◽  
Kevin L. Schauer ◽  
Dain R. Brademan ◽  
Nicholas M. Riley ◽  
Evgenia Shishkova ◽  
...  

2021 ◽  
Author(s):  
Jonathan Steven Dhenin ◽  
Diogo Borges Lima ◽  
Mathieu Dupre ◽  
Julia Chamot-Rooke

We present a new software-tool allowing an easy visualization of fragment ions and thus a rapid evaluation of key experimental parameters on the sequence coverage obtained for the MS/MS analysis of intact proteins. Our tool can deal with multiple fragmentation methods. We demonstrate that TDFragMapper can rapidly highlight the experimental fragmentation parameters that are critical to the characterization of intact proteins of various size using top-down proteomics. TDFragMapper, a demonstration video and user tutorial are freely available at https://msbio.pasteur.fr/tdfragmapper, for academic use; all data are thus available from the ProteomeXchange consorti-um (identifier PXD024643).


2014 ◽  
Vol 86 (3) ◽  
pp. 1485-1492 ◽  
Author(s):  
Kenneth R. Durbin ◽  
Ryan T. Fellers ◽  
Ioanna Ntai ◽  
Neil L. Kelleher ◽  
Philip D. Compton

2008 ◽  
Vol 80 (5) ◽  
pp. 1459-1467 ◽  
Author(s):  
Maureen K. Bunger ◽  
Benjamin J. Cargile ◽  
Anne Ngunjiri ◽  
Jonathan L. Bundy ◽  
James L. Stephenson

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