2017
DOI: 10.3390/proteomes5030018
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Editorial for Special Issue: Approaches to Top-Down Proteomics: In Honour of Prof. Patrick H. O’Farrell

Abstract: Presaging the current discipline of Proteomics, Prof Patrick H. O’Farrell recognized the critical need for detailed protein analyses to dissect and thereby understand molecular mechanisms. [...]

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Cited by 4 publications
(8 citation statements)
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“…Thus, while bottom-up may serve as a rapid, low-resolution scan of a proteome, it enables deep, high-resolution proteome analyses when paired with two-dimensional gel electrophoresis (2DE). The 2DE protocol was developed in 1975, essentially initiating the discipline of proteomics [ 92 , 93 ]. Since inception, this method has also received its share of criticism, mainly around original issues concerning the resolution of low abundance proteoforms with extreme p I and MW, and hydrophobic protein species [ 73 , 94 , 95 ].…”
Section: Discovery Proteomicsmentioning
confidence: 99%
“…Thus, while bottom-up may serve as a rapid, low-resolution scan of a proteome, it enables deep, high-resolution proteome analyses when paired with two-dimensional gel electrophoresis (2DE). The 2DE protocol was developed in 1975, essentially initiating the discipline of proteomics [ 92 , 93 ]. Since inception, this method has also received its share of criticism, mainly around original issues concerning the resolution of low abundance proteoforms with extreme p I and MW, and hydrophobic protein species [ 73 , 94 , 95 ].…”
Section: Discovery Proteomicsmentioning
confidence: 99%
“…The serum proteome based cancer biomarkers are soluble molecules secreted (and/or shed off) into the blood stream by cancer cells or other cell types belonging to the tumor microenvironment. 23,[103][104][105] The quantification of such biomarker molecules is economic; such serum based noninvasive diagnostic assays may correlate with the oral precancerous or OSCC cancerous pathologies. [103][104][105] The five differential serum spots were identified as four proteins DNAJC13, SSFA2-IV, UPF0415, and KRT-1.…”
Section: Discussionmentioning
confidence: 99%
“…102 In head and neck cancers HPV16 genome exits in three states: episomes, integrated and hybrid episomes. 91 The [103][104][105] The five differential serum spots were identified as four proteins DNAJC13, SSFA2-IV, UPF0415, and KRT-1. Two amongst five serum protein spots were identified as SSFA2-IV.…”
Section: Discussionmentioning
confidence: 99%
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