2019
DOI: 10.1039/c8ra07200k
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Middle-down approach: a choice to sequence and characterize proteins/proteomes by mass spectrometry

Abstract: Enhanced sequence coverage, better identification of combinatorial co-occurring PTMs and improved detection of proteoforms are key highlights of middle-down approach and hence, this can be a promiscuous approach for protein sequencing and proteomics.

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Cited by 56 publications
(41 citation statements)
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References 290 publications
(547 reference statements)
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“…Hair Identify ethnic groups [18,36,37] Distinguish gender [26] Distinguish individuals [27,38,39] and middle-down proteomics can be found in some literature reviews (e.g., [58,59] for top-down and [56] for middle-down proteomics). An overview of general methods for bottom-up proteomics is presented in Figure 1 [23].…”
Section: Sample Type Applicationsmentioning
confidence: 99%
“…Hair Identify ethnic groups [18,36,37] Distinguish gender [26] Distinguish individuals [27,38,39] and middle-down proteomics can be found in some literature reviews (e.g., [58,59] for top-down and [56] for middle-down proteomics). An overview of general methods for bottom-up proteomics is presented in Figure 1 [23].…”
Section: Sample Type Applicationsmentioning
confidence: 99%
“…Currently, mass spectrometry techniques (by means of bottom-up, top-down and middle-down strategies) are able to evaluate the status of protein modification, including their site location (Olsen and Mann 2013;Pascovici et al 2018). The bottom-up MS approach consists of analyzing the resulting peptides (0.8-3 kDa) from previous enzymatic or chemical cleavage and it has been widely used for qualitative analysis of new PTM (Lanucara and Eyers 2013;Pandeswari and Sabareesh 2019). This bottom-up MS approach is a very suitable technique to identify, locate and quantify modified peptides, although it has some limitations mainly concerning the combinatorial effect of several PTM.…”
Section: Techniques To Identify Post-translational Modifications Of Allergensmentioning
confidence: 99%
“…In contrast to TD and MD proteomics analysis, for BU data analysis, a deconvolution step is not required when implementing ESI, due to the rare generation of double-and triple-charged fragment ions (36). Mass spectra raw data are commonly processed by Proteome Discoverer or MaxQuant platforms using several search engines, such as Sequest, Mascot, Andromeda, X!Tandem and COMET, usually against UniProt databases (37)(38)(39).…”
Section: Bottom-up Data Analysismentioning
confidence: 99%