4.5 Article

Chemical Tools for Temporally and Spatially Resolved Mass Spectrometry-Based Proteomics

Journal

ANNALS OF BIOMEDICAL ENGINEERING
Volume 42, Issue 2, Pages 299-311

Publisher

SPRINGER
DOI: 10.1007/s10439-013-0878-3

Keywords

Protein synthesis; BONCAT; SILAC; APEX

Funding

  1. National Institutes of Health [NIH R01 GM062523]
  2. Institute for Collaborative Biotechnologies through grant from U.S. Army Research Office [W911NF-09-0001]

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Accurate measurements of the abundances, synthesis rates and degradation rates of cellular proteins are critical for understanding how cells and organisms respond to changes in their environments. Over the past two decades, there has been increasing interest in the use of mass spectrometry for proteomic analysis. In many systems, however, protein diversity as well as cell and tissue heterogeneity limit the usefulness of mass spectrometry-based proteomics. As a result, researchers have had difficulty in systematically identifying proteins expressed within specified time intervals, or low abundance proteins expressed in specific tissues or in a few cells in complex microbial systems. In this review, we present recently-developed tools and strategies that probe these two subsets of the proteome: proteins synthesized during well-defined time intervals-temporally resolved proteomics-and proteins expressed in predetermined cell types, cells or cellular compartments-spatially resolved proteomics-with a focus on chemical and biological mass spectrometry-based methodologies.

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