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Liposomes, Exosomes, and Virosomes: From Modeling Complex

Membrane Processes to Medical Diagnostics and Drug Delivery

Tuesday Speaker Abstracts

29

Mechanics of Extracellular Vesicles from Plasmodium Falciparum Infected Red Blood

Cells

Raya Sorkin

1

, Daan Vorselen

1

, Yifat Ofir-Birin

2

, Wouter Roos

1

, Fred MacKintosh

1

, Neta

Regev-Rudzki

2

, Gijs Wuite

1

.

1

VU University Amsterdam, Amsterdam, Netherlands,

2

Weizmann Institute of Science, Rehovot,

Israel.

Malaria is a life-threatening disease caused by parasites that are transmitted through the bites of

infected mosquitoes, with Plasmodium falciparum (Pf) causing the most severe form of malaria

(1). Very recently it was discovered that Pf infected red blood cells (iRBC) directly transfer

information between parasites within a population using exosome like-vesicles that are capable

of delivering genes (2). This communication promotes parasite differentiation to sexual forms

and is critical for its survival in the host and transmission to mosquitoes.

Efficient DNA transfer via extracellular vesicles (EVs) occurs mainly at the early ring stage

within the blood-stage asexual cycle, and it can be inhibited by addition of actin polymerization

inhibitors. This suggests that actin polymerization is required for cell-cell communication (2).

We expect, therefore, that mechanical properties of vesicles at different stages of the life cycle

will be optimized for their function, and more specifically, the stiffness of the ring stage EVs is

likely better optimized for efficient DNA-dependent communication. With the aim to understand

how mechanical properties of EVs effect their efficiency of cargo delivery, we use Atomic Force

Microscopy for mechanical characterization of extracellular vesicles secreted from Pf infected

RBCs. We perform a detailed comparison between the mechanical properties (bending modulus

values) of these vesicles and those secreted from healthy RBCs, as well as compare their size and

morphology. We also prepare and characterize synthetic vesicles (SVs) with varying mechanical

strength to determine how stiffness of SVs affects their adhesion to cells and cellular uptake rate,

to gain a broader understanding of the link between mechanical properties and efficient cellular

uptake.

1. WHO

http://www.who.int/mediacentre/factsheets/fs094/en/.

2. N. Regev-Rudzki et al., Cell 153, 1120 (May 23, 2013).

Phase Transitions: An Emerging Principle in Cytoplasmic Organization and

Neurodegeneration

Anthony Hyman

Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany

No Abstract