Mass spectrometry-based methods for analysing the mitochondrial interactome in mammalian cells

被引:10
作者
Koshiba, Takumi [1 ]
Kosako, Hidetaka [2 ]
机构
[1] Fukuoka Univ, Dept Chem, Fac Sci, Fukuoka 8140180, Japan
[2] Tokushima Univ, Fujii Mem Inst Med Sci, Div Cell Signaling, Tokushima, Tokushima 7708503, Japan
关键词
BioID; mass spectrometry; mitochondria; proteome; XL-MS; CROSS-LINKING; CONTACT SITE; BIOTIN LIGASE; PROTEINS; TECHNOLOGY; COMPLEX; SYSTEM;
D O I
10.1093/jb/mvz090
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Protein-protein interactions are essential biologic processes that occur at inter- and intracellular levels. To gain insight into the various complex cellular functions of these interactions, it is necessary to assess them under physiologic conditions. Recent advances in various proteomic technologies allow to investigate protein-protein interaction networks in living cells. The combination of proximity-dependent labelling and chemical cross-linking will greatly enhance our understanding of multi-protein complexes that are difficult to prepare, such as organelle-bound membrane proteins. In this review, we describe our current understanding of mass spectrometry-based proteomics mapping methods for elucidating organelle-bound membrane protein complexes in living cells, with a focus on protein-protein interactions in mitochondrial subcellular compartments.
引用
收藏
页码:225 / 231
页数:7
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