Moving Profiling Spatial Proteomics Beyond Discrete Classification

被引:17
作者
Crook, Oliver M. [1 ]
Smith, Tom [1 ]
Elzek, Mohamed [1 ]
Lilley, Kathryn S. [1 ]
机构
[1] Univ Cambridge, Dept Biochem, Cambridge Ctr Prote, Cambridge, England
基金
英国生物技术与生命科学研究理事会;
关键词
organelle; protein localization; PROTEIN SUBCELLULAR-LOCALIZATION; ORGANELLE PROTEOME; FRACTIONATION; REVEALS; MAP;
D O I
10.1002/pmic.201900392
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The spatial subcellular proteome is a dynamic environment; one that can be perturbed by molecular cues and regulated by post-translational modifications. Compartmentalization of this environment and management of these biomolecular dynamics allows for an array of ancillary protein functions. Profiling spatial proteomics has proved to be a powerful technique in identifying the primary subcellular localization of proteins. The approach has also been refashioned to study multi-localization and localization dynamics. Here, the analytical approaches that have been applied to spatial proteomics thus far are critiqued, and challenges particularly associated with multi-localization and dynamic relocalization is identified. To meet some of the current limitations in analytical processing, it is suggested that Bayesian modeling has clear benefits over the methods applied to date and should be favored whenever possible. Careful consideration of the limitations and challenges, and development of robust statistical frameworks, will ensure that profiling spatial proteomics remains a valuable technique as its utility is expanded.
引用
收藏
页数:10
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