{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"institution":[{"name":"bioRxiv"}],"indexed":{"date-parts":[[2026,7,30]],"date-time":"2026-07-30T17:26:41Z","timestamp":1785432401354,"version":"3.56.0"},"posted":{"date-parts":[[2025,4,27]]},"group-title":"Biophysics","reference-count":74,"publisher":"openRxiv","license":[{"start":{"date-parts":[[2025,4,27]],"date-time":"2025-04-27T00:00:00Z","timestamp":1745712000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"funder":[{"award":["R35GM133764"],"award-info":[{"award-number":["R35GM133764"]}],"id":[{"id":"https:\/\/ror.org\/04q48ey07","id-type":"ROR","asserted-by":"publisher"}]},{"award":["R35GM147491"],"award-info":[{"award-number":["R35GM147491"]}],"id":[{"id":"https:\/\/ror.org\/04q48ey07","id-type":"ROR","asserted-by":"publisher"}]},{"award":["R21AI185746"],"award-info":[{"award-number":["R21AI185746"]}],"id":[{"id":"https:\/\/ror.org\/043z4tv69","id-type":"ROR","asserted-by":"publisher"}]},{"award":["T32AI055434"],"award-info":[{"award-number":["T32AI055434"]}],"id":[{"id":"https:\/\/ror.org\/043z4tv69","id-type":"ROR","asserted-by":"publisher"}]},{"award":["U54DK110858"],"award-info":[{"award-number":["U54DK110858"]}],"id":[{"id":"https:\/\/ror.org\/00adh9b73","id-type":"ROR","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"accepted":{"date-parts":[[2025,10,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                <jats:p>Malaria parasites infect red blood cells where they digest host hemoglobin and release free heme inside a lysosome-like organelle called the food vacuole. To detoxify excess heme, parasites form hemozoin crystals that rapidly tumble inside this compartment. Hemozoin formation is critical for parasite survival and central to antimalarial drug activity. Although the static structural properties of hemozoin have been extensively investigated, crystal motion and its underlying mechanism have remained puzzling. We used quantitative image analysis to determine the timescale of motion, which requires the intact vacuole but does not require the parasite itself. Using single particle tracking and Brownian dynamics simulations with experimentally derived interaction potentials, we found that hemozoin motion exhibits unexpectedly tight confinement but is much faster than thermal diffusion. Hydrogen peroxide, which is generated at high levels in the food vacuole, has been shown to stimulate the motion of synthetic metallic nanoparticles via surface-catalyzed peroxide decomposition that generates propulsive kinetic energy. We observed that peroxide stimulated the motion of isolated crystals in solution and that conditions that suppress peroxide formation slowed hemozoin motion inside parasites. These data suggest that surface-exposed metals on hemozoin catalyze peroxide decomposition to drive crystal motion. This work reveals hemozoin motion in malaria parasites as a biological example of an endogenous self-propelled nanoparticle. This mechanism of propulsion likely serves a physiological role to reduce oxidative stress to parasites from hydrogen peroxide produced by large-scale hemoglobin digestion during blood-stage infection.<\/jats:p>\n                <jats:sec>\n                  <jats:title>Significance statement<\/jats:title>\n                  <jats:p>\n                    Hemozoin crystal formation is a major antimalarial drug target as it is essential for survival of\n                    <jats:italic>Plasmodium<\/jats:italic>\n                    parasites that cause malaria, one of the world\u2019s most devastating infectious diseases. Hemozoin crystals rapidly tumble inside the parasite food vacuole, and the mechanism and significance of this motion have been mysterious. Using quantitative live-cell imaging and computational modeling, we discovered that hemozoin motion is driven by catalytic decomposition of hydrogen peroxide on the crystal surface, a mechanism analogous to synthetic nanomotors. Hemozoin crystals have been viewed as inert detoxification products. Our work reframes the physiological role of these crystals as catalytically active nanoparticles whose mechanism of propulsion helps to neutralize toxic hydrogen peroxide generated by parasite digestion of hemoglobin during blood-stage infection.\n                  <\/jats:p>\n                <\/jats:sec>","DOI":"10.1101\/2025.04.25.650681","type":"posted-content","created":{"date-parts":[[2025,4,28]],"date-time":"2025-04-28T00:30:16Z","timestamp":1745800216000},"source":"Crossref","is-referenced-by-count":1,"title":["Chemical propulsion of hemozoin crystal motion in malaria parasites"],"prefix":"10.64898","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-8063-2849","authenticated-orcid":false,"given":"Erica M.","family":"Hastings","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-4394-4928","authenticated-orcid":false,"given":"Tomasz","family":"Skora","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-3508-6313","authenticated-orcid":false,"given":"Keith R.","family":"Carney","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-3543-7128","authenticated-orcid":false,"given":"Henry C.","family":"Fu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-7096-4839","authenticated-orcid":false,"given":"Tamara C.","family":"Bidone","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-3464-3042","authenticated-orcid":false,"given":"Paul A.","family":"Sigala","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"54368","reference":[{"key":"2025100605050511000_2025.04.25.650681v2.1","doi-asserted-by":"crossref","first-page":"e214","DOI":"10.1016\/S2666-5247(24)00016-8","article-title":"The 2023 WHO World malaria report","volume":"5","year":"2024","journal-title":"Lancet Microbe"},{"key":"2025100605050511000_2025.04.25.650681v2.2","doi-asserted-by":"publisher","DOI":"10.1016\/j.pt.2022.02.010"},{"key":"2025100605050511000_2025.04.25.650681v2.3","doi-asserted-by":"publisher","DOI":"10.1038\/35005132"},{"key":"2025100605050511000_2025.04.25.650681v2.4","doi-asserted-by":"publisher","DOI":"10.1016\/S0166-6851(03)00163-4"},{"key":"2025100605050511000_2025.04.25.650681v2.5","doi-asserted-by":"publisher","DOI":"10.1073\/pnas.93.21.11865"},{"key":"2025100605050511000_2025.04.25.650681v2.6","doi-asserted-by":"publisher","DOI":"10.1016\/j.pt.2016.05.010"},{"key":"2025100605050511000_2025.04.25.650681v2.7","first-page":"1","article-title":"Effects of antimalarial drugs on movement of Plasmodium falciparum","volume":"43","year":"2012","journal-title":"Southeast Asian J Trop Med Public Health"},{"key":"2025100605050511000_2025.04.25.650681v2.8","doi-asserted-by":"publisher","DOI":"10.3109\/01913123.2011.601405"},{"key":"2025100605050511000_2025.04.25.650681v2.9","doi-asserted-by":"publisher","DOI":"10.1073\/pnas.2001153117"},{"key":"2025100605050511000_2025.04.25.650681v2.10","doi-asserted-by":"publisher","DOI":"10.1016\/j.celrep.2020.107817"},{"key":"2025100605050511000_2025.04.25.650681v2.11","doi-asserted-by":"crossref","unstructured":"P. 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