Activity-Based Protein Profiling for the Study of Parasite Biology

被引:7
作者
Benns, Henry J. [1 ]
Tate, Edward W. [1 ]
Child, Matthew A. [2 ]
机构
[1] Imperial Coll London, Dept Chem, Exhibit Rd, London SW7 2AZ, England
[2] Imperial Coll London, Life Sci, Exhibit Rd, London SW7 2AZ, England
来源
ACTIVITY-BASED PROTEIN PROFILING | 2019年 / 420卷
基金
英国生物技术与生命科学研究理事会;
关键词
PLASMODIUM-FALCIPARUM; CYSTEINE PROTEASE; TRYPANOSOMA-BRUCEI; CHEMICAL METHODS; DRUG-RESISTANCE; SERINE-PROTEASE; IDENTIFICATION; PLASMEPSINS; INHIBITORS; INVASION;
D O I
10.1007/82_2018_123
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
Parasites exist within most ecological niches, often transitioning through biologically and chemically complex host environments over the course of their parasitic life cycles. While the development of technologies for genetic engineering has revolutionised the field of functional genomics, parasites have historically been less amenable to such modification. In light of this, parasitologists have often been at the forefront of adopting new small-molecule technologies, repurposing drugs into biological tools and probes. Over the last decade, activity-based protein profiling (ABPP) has evolved into a powerful and versatile chemical proteomic platform for characterising the function of enzymes. Central to ABPP is the use of activity-based probes (ABPs), which covalently modify the active sites of enzyme classes ranging from serine hydrolases to glycosidases. The application of ABPP to cellular systems has contributed vastly to our knowledge on the fundamental biology of a diverse range of organisms and has facilitated the identification of potential drug targets in many pathogens. In this chapter, we provide a comprehensive review on the different forms of ABPP that have been successfully applied to parasite systems, and highlight key biological insights that have been enabled through their application.
引用
收藏
页码:155 / 174
页数:20
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