| Literature DB >> 26025769 |
Casey L Kohnhorst1, Danielle L Schmitt1, Anand Sundaram1, Songon An2.
Abstract
A cell is a highly organized, dynamic, and intricate biological entity orchestrated by a myriad of proteins and their self-assemblies. Because a protein's actions depend on its coordination in both space and time, our curiosity about protein functions has extended from the test tube into the intracellular space of the cell. Accordingly, modern technological developments and advances in enzymology have been geared towards analyzing protein functions within intact single cells. We discuss here how fluorescence single-cell microscopy has been employed to identify subcellular locations of proteins, detect reversible protein-protein interactions, and measure protein activity and kinetics in living cells. Considering that fluorescence single-cell microscopy has been only recently recognized as a primary technique in enzymology, its potentials and outcomes in studying intracellular protein functions are projected to be immensely useful and enlightening. We anticipate that this review would inspire many investigators to study their proteins of interest beyond the conventional boundary of specific disciplines. This article is part of a Special Issue entitled: Physiological Enzymology and Protein Functions.Entities:
Keywords: Colocalization; Enzyme kinetics; Fluorescence microscopy; Genetically-encoded fluorescent tag; Protein activity; Protein–protein interaction; Subcellular localization
Mesh:
Year: 2015 PMID: 26025769 PMCID: PMC5679394 DOI: 10.1016/j.bbapap.2015.05.014
Source DB: PubMed Journal: Biochim Biophys Acta ISSN: 0006-3002