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Scientists characterise Myosin A motor to assess its importance in parasite mobility and researchers stress the need to evaluate both the quality and quantity of induced antibodies to determine vaccine efficacy.
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The mobility of the malaria parasite relies on a macromolecular complex called the glideosome, of which a particular compound, Myosin A motor, plays a crucial part. New research has characterised Myosin A’s structure and found that the priming of it in the early stages of infection results in specific lever arm and motor domain interactions that allow for more effective parasite movement. Targeting these molecules could, therefore, prevent the escalation of infection.
It’s long been understood that the amount of antibody that a vaccine produces is a strong indicator of its efficacy. New research has found that changing the dosing pattern of the RTS,S malaria vaccine offered greater protective immunity but did not change the concentration of antibodies. These results emphasise the need to evaluate both the quality and quantity of the antibodies as a more reliable indicator of vaccine success.
Full-Length Plasmodium falciparum Myosin A and Essential Light Chain PfELC Structures Provide New Anti-Malarial Targets
Modelling the Roles of Antibody Titre and Avidity in Protection From Plasmodium falciparum Malaria Infection Following RTS,S/AS01 Vaccination
Image Credits: CDC/ Dr. Mae Melvin 
Scientific Advisor: Elena Gómez-Díaz, Institute of Parasitology and Biomedicine, Spain
The post Molecules That Aid Parasite Movement Could Provide New Drug Targets appeared first on The Fight Malaria Blog.