한빛사논문
- 조회649
Byung Rho Lee1 Tae Jin Lee2 Sekyung Oh3 Chenglong Li1 Jin-Hyuk A Song1 Brendan Marshall1 Wenbo Zhi2 Sang-Ho Kwon1*
1Department of Cellular Biology and Anatomy, Medical College of Georgia, Augusta University, Augusta, Georgia, USA
2Center for Biotechnology and Genomic Medicine, Medical College of Georgia, Augusta University, Augusta, Georgia, USA
3Department of Medical Science, Catholic Kwandong University College of Medicine, Incheon, South Korea
Byung Rho Lee, Tae Jin Lee and Sekyung Oh contributed equally to this study.
*Corresponding author.
Abstract
The extracellular vesicle exosome mediates intercellular communication by transporting macromolecules such as proteins and ribonucleic acids (RNAs). Determining cargo contents with high accuracy will help decipher the biological processes that exosomes mediate in various contexts. Existing methods for probing exosome cargo molecules rely on a prior exosome isolation procedure. Here we report an in situ labelling approach for exosome cargo identification, which bypasses the exosome isolation steps. In this methodology, a variant of the engineered ascorbate peroxidase APEX, fused to an exosome cargo protein such as CD63, is expressed specifically in exosome-generating vesicles in live cells or in secreted exosomes in the conditioned medium, to induce biotinylation of the proteins in the vicinity of the APEX variant for a short period of time. Mass spectrometry analysis of the proteins biotinylated by this approach in exosomes secreted by kidney proximal tubule-derived cells reveals that oxidative stress can cause ribosomal proteins to accumulate in an exosome subpopulation that contains the CD63-fused APEX variant.
논문정보
- Research article
- 2022년 06월 (BRIC 등록일 2022-08-04)
- 국내+국외 연구진
- 생명과학 > 세포생물학
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