Abstract:
:The engineered ascorbate peroxidase (APEX) is a powerful tool for the proximity-dependent labeling of proteins and RNAs in live cells. Although widely use in mammalian cells, APEX applications in microorganisms have been hampered by the poor labeling efficiency of its biotin-phenol (BP) substrate. In this study, we sought to address this challenge by designing and screening a panel of alkyne-functionalized substrates. Our best probe, Alk-Ph, substantially improves APEX-labeling efficiency in intact yeast cells, as it is more cell wall-permeant than BP. Through a combination of protein-centric and peptide-centric chemoproteomic experiments, we have identified 165 proteins with a specificity of 94% in the yeast mitochondrial matrix. In addition, we have demonstrated that Alk-Ph is useful for proximity-dependent RNA labeling in yeast, thus expanding the scope of APEX-seq. We envision that this improved APEX-labeling strategy would set the stage for the large-scale mapping of spatial proteome and transcriptome in yeast.
journal_name
Cell Chem Bioljournal_title
Cell chemical biologyauthors
Li Y,Tian C,Liu K,Zhou Y,Yang J,Zou Pdoi
10.1016/j.chembiol.2020.05.006subject
Has Abstractpub_date
2020-07-16 00:00:00pages
858-865.e8issue
7eissn
2451-9456issn
2451-9448pii
S2451-9456(20)30152-5journal_volume
27pub_type
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