J-dot targeting of an exported HSP40 in Plasmodium falciparum-infected erythrocytes
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文摘

We examine the targeting of exported HSP40 to J-dots.

We found that the substrate binding domain (SBD) is necessary and required for J-dot targeting.

Targeting is independent of endogenous protein.

The minimal construct associates with the exported chaperone PfHsp70x.

J-dots are likely Plasmodium falciparum-specific.

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