Recent advances in chemical biology tools for protein and RNA profiling of extracellular vesicles

被引:1
|
作者
Lim, Woojeong [1 ]
Lee, Soyeon [1 ]
Koh, Minseob [2 ]
Jo, Ala [3 ]
Park, Jongmin [1 ,4 ,5 ]
机构
[1] Kangwon Natl Univ, Dept Chem Engn, Chuncheon Si 24341, South Korea
[2] Pusan Natl Univ, Dept Chem, Busan 46241, South Korea
[3] Inst for Basic Sci Korea, Ctr Nanomed, Seoul 03722, South Korea
[4] Kangwon Natl Univ, Inst Mol Sci & Fus Technol, Chunchon 24341, South Korea
[5] Kangwon Natl Univ, Multidimens Genom Res Ctr, Chunchon 24341, South Korea
来源
RSC CHEMICAL BIOLOGY | 2024年 / 5卷 / 06期
基金
新加坡国家研究基金会;
关键词
PROGENITOR CELLS; DRUG-DELIVERY; EXOSOMES; MICROVESICLES; PH; BIOGENESIS; METAMATERIALS; TECHNOLOGIES; CHALLENGES; BIOMARKERS;
D O I
10.1039/d3cb00200d
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
Extracellular vesicles (EVs) are nano-sized vesicles secreted by cells that contain various cellular components such as proteins, nucleic acids, and lipids from the parent cell. EVs are abundant in body fluids and can serve as circulating biomarkers for a variety of diseases or as a regulator of various biological processes. Considering these characteristics of EVs, analysis of the EV cargo has been spotlighted for disease diagnosis or to understand biological processes in biomedical research. Over the past decade, technologies for rapid and sensitive analysis of EVs in biofluids have evolved, but detection and isolation of targeted EVs in complex body fluids is still challenging due to the unique physical and biological properties of EVs. Recent advances in chemical biology provide new opportunities for efficient profiling of the molecular contents of EVs. A myriad of chemical biology tools have been harnessed to enhance the analytical performance of conventional assays for better understanding of EV biology. In this review, we will discuss the improvements that have been achieved using chemical biology tools. This review provides an overview of how chemical biology tools have been applied for efficient EV isolation, the increment of EV detection sensitivity, multiplexed analysis of EV protein, metabolic labeling of EVs, and drug occupancy of EV proteins.
引用
收藏
页码:483 / 499
页数:18
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