7 research outputs found

    Dot plots showing complement activation by fractions eluted at different EDTA concentrations.

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    <p>The 50 mM fraction (Panel D) had maximal activity that was comparable to that of the crude culture supernatant (Panel A). Sham supernatant eluted at 50 mM EDTA had no complement activity.</p

    Silver stained PAGE gel showing three distinct proteins of sizes 40–64 kDa.

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    <p>Lanes marked MWβ€Š=β€Š molecular weight marker, 1β€Š=β€Š crude <i>P. falciparum</i> culture supernatant, 2β€Š=β€Š MBL binding proteins eluted with 50 mM EDTA.</p

    Photomicrographs showing C3b deposition on erythrocytes (fluorescent spots) following activation of complement by supernatant from sham culture (Panel A) and <i>P. falciparum</i> culture (Panel B) harvested at schizont stage.

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    <p>Note the fluorescent spots are in clusters, which is the hallmark of CR1 distribution on erythrocytes <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0105093#pone.0105093-Taylor1" target="_blank">[33]</a>. C3b was detected by Alexa 488 conjugated to anti-C3b IgG, and observed under high power magnification using an Olympus BX41 fluorescent microscope (Olympus America Inc. USA).</p

    Representative dot plots showing % C3b deposition on RBC following complement activation by sham and malaria culture supernatants at 2% parasitemia.

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    <p>% C3b deposition for sham supernatant was (3.77%), rings (8.22%), late trophozoites (11.10%) and schizontes (17.70%).</p

    Merozoite lectin binding proteins identified by Matrix-assisted laser desorption/ionization (MALDI).

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    <p>Merozoite lectin binding proteins identified by Matrix-assisted laser desorption/ionization (MALDI).</p
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