Bioanalysis of Eukaryotic Organelles

被引：115

作者：

Satori, Chad P. ^{[1
]}

Henderson, Michelle M. ^{[1
]}

Krautkramer, Elyse A. ^{[1
]}

Kostal, Vratislav ^{[2
,3
]}

Distefano, Mark M. ^{[1
]}

Arriaga, Edgar A. ^{[1
]}

机构：

[1] Univ Minnesota, Dept Chem, Minneapolis, MN 55455 USA

[2] Tescan, Brno 62300, Czech Republic

[3] Inst Analyt Chem ASCR, Brno 60200, Czech Republic

来源：

CHEMICAL REVIEWS | 2013年 / 113卷 / 04期

基金：

美国国家卫生研究院;

关键词：

GREEN FLUORESCENT PROTEIN; ATOMIC-FORCE MICROSCOPY; CAPILLARY ELECTROPHORETIC ANALYSIS; GOLGI NETWORK/EARLY ENDOSOME; ENDOPLASMIC-RETICULUM STRESS; INTEGRAL MEMBRANE-PROTEINS; MASS-SPECTRAL DATA; SUBCELLULAR-LOCALIZATION; OXIDATIVE STRESS; PHAGOSOME MATURATION;

D O I：

10.1021/cr300354g

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The role that organelle analysis has played in understanding biology is studied. Organelle analysis enables a more specific description of the molecular, biochemical, and physiological processes associated with diseases, embryonic development, tissue differentiation, organism aging, disease treatments, and organism response to pathogens. Confocal microscopy has become a routine tool for investigating subcellular organization, organelle networks, and organelle dynamics in cellular and tissue samples. Most organelles have a dynamic, three-dimensional (3D) organization inside the cell, which is tightly connected to their physiological functions. Due to this, a single 2D image inherently limits the information acquired about the distribution of a particular property within the organelle. The combination of subcellular fractionation with 'omic' technologies has become a powerful resource to characterize and catalogue the various subcellular environments in a cell.

引用

页码：2733 / 2811

页数：79

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