High-throughput Proteomics and Protein Biomarker Discovery in an Experimental Model of Inflammatory Hyperalgesia

Drugs ◽  
2003 ◽  
Vol 63 (Supplement 1) ◽  
pp. 23-29 ◽  
Author(s):  
C Gineste ◽  
L Ho ◽  
P Pompl ◽  
M Bianchi ◽  
G M Pasinetti
2017 ◽  
Vol 6 (1) ◽  
pp. 1369805 ◽  
Author(s):  
Joanne L. Welton ◽  
Samantha Loveless ◽  
Timothy Stone ◽  
Chris von Ruhland ◽  
Neil P. Robertson ◽  
...  

2021 ◽  
Author(s):  
Ernesto S. Nakayasu ◽  
Marina Gritsenko ◽  
Paul D. Piehowski ◽  
Yuqian Gao ◽  
Daniel J. Orton ◽  
...  

Author(s):  
Lan Huang ◽  
Dan Shao ◽  
Yan Wang ◽  
Xueteng Cui ◽  
Yufei Li ◽  
...  

Abstract Empowered by the advancement of high-throughput bio technologies, recent research on body-fluid proteomes has led to the discoveries of numerous novel disease biomarkers and therapeutic drugs. In the meantime, a tremendous progress in disclosing the body-fluid proteomes was made, resulting in a collection of over 15 000 different proteins detected in major human body fluids. However, common challenges remain with current proteomics technologies about how to effectively handle the large variety of protein modifications in those fluids. To this end, computational effort utilizing statistical and machine-learning approaches has shown early successes in identifying biomarker proteins in specific human diseases. In this article, we first summarized the experimental progresses using a combination of conventional and high-throughput technologies, along with the major discoveries, and focused on current research status of 16 types of body-fluid proteins. Next, the emerging computational work on protein prediction based on support vector machine, ranking algorithm, and protein–protein interaction network were also surveyed, followed by algorithm and application discussion. At last, we discuss additional critical concerns about these topics and close the review by providing future perspectives especially toward the realization of clinical disease biomarker discovery.


RSC Advances ◽  
2019 ◽  
Vol 9 (6) ◽  
pp. 3351-3358 ◽  
Author(s):  
Qun Liang ◽  
Han Liu ◽  
Xiuli Li ◽  
Panguo Hairong ◽  
Peiyang Sun ◽  
...  

High-throughput metabolic profiling technology has been used for biomarker discovery and to reveal underlying metabolic mechanisms.


2010 ◽  
Vol 73 (10) ◽  
pp. 1790-1803 ◽  
Author(s):  
Tieneke B.M. Schaaij-Visser ◽  
Ruud H. Brakenhoff ◽  
C. René Leemans ◽  
Albert J.R. Heck ◽  
Monique Slijper

2017 ◽  
Vol 2017 ◽  
pp. 1-9 ◽  
Author(s):  
Ze-ying Wu ◽  
Zhong-da Zeng ◽  
Zi-dan Xiao ◽  
Daniel Kam-Wah Mok ◽  
Yi-zeng Liang ◽  
...  

The rapid increase in the use of metabolite profiling/fingerprinting techniques to resolve complicated issues in metabolomics has stimulated demand for data processing techniques, such as alignment, to extract detailed information. In this study, a new and automated method was developed to correct the retention time shift of high-dimensional and high-throughput data sets. Information from the target chromatographic profiles was used to determine the standard profile as a reference for alignment. A novel, piecewise data partition strategy was applied for the determination of the target components in the standard profile as markers for alignment. An automated target search (ATS) method was proposed to find the exact retention times of the selected targets in other profiles for alignment. The linear interpolation technique (LIT) was employed to align the profiles prior to pattern recognition, comprehensive comparison analysis, and other data processing steps. In total, 94 metabolite profiles of ginseng were studied, including the most volatile secondary metabolites. The method used in this article could be an essential step in the extraction of information from high-throughput data acquired in the study of systems biology, metabolomics, and biomarker discovery.


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