Intrinsically Disordered Malaria Antigens: An Overview of Structures, Dynamics and Molecular Simulation Opportunities

被引:1
作者
da Silva, Pamella C. C. [1 ,2 ]
Martinez, Leandro [1 ,2 ]
机构
[1] Univ Estadual Campinas UNICAMP, Inst Quim, BR-13083970 Campinas, SP, Brazil
[2] Univ Estadual Campinas UNICAMP, Ctr Comp Engn & Ciencias, BR-13083970 Campinas, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Plasmodium falciparum; molecular dynamics; enhanced sampling methods; antigen-antibody interactions; intrinsically disordered proteins; FREE-ENERGY CALCULATIONS; MEROZOITE SURFACE PROTEIN-1; VACCINE CANDIDATE PFS48/45; SEQUENCE-BASED PREDICTION; C-TERMINAL FRAGMENT; PLASMODIUM-FALCIPARUM; FORCE-FIELD; MONOCLONAL-ANTIBODY; REPLICA-EXCHANGE; BINDING-SITES;
D O I
10.21577/0103-5053.20240102
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The proteome of Plasmodium falciparum ( Pf ) is abundant in intrinsically disordered proteins (IDPs). Their important roles in the malaria life cycle and the limitations of experimental and computational methods to study this class of proteins hinder the development of antimalarial drugs. At the same time, the growing interest in IDPs and theoretical tools suggest a path for their classification and functional understanding: searching databases with experimental notes and predictions of protein disorder, developing force fields to describe protein flexibility, and using molecular dynamics enhanced sampling techniques to properly sample the IDP conformational diversity. This review discusses possibilities of exploration of Pf 's IDPs and their availability in disordered-protein databases to foster molecular modeling studies. The large percentage of intrinsic disorder present in many antigens and their ability to interact with different targets, make these proteins a major class of interest in the area of drug and vaccine development.
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页数:21
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