• Regev-Rudzki, Neta
• Mullick, Debakshi
• Zhang, Peijun
• Houben, Lothar
• Biran, Idan
• Marom, Noa
• Owen, David
• Gruene, Tim
• Klar, Paul Benjamin
• Waterman, David
• Gilchrist, James B.
• Palatinus, Lukas
• Leiserowitz, Leslie
• Dzikowski, Ron
• Wen, Wen

Abstract

<jats:title>Abstract</jats:title><jats:p>Detoxification of heme in Plasmodium depends on its crystallization into hemozoin. This pathway is a major target of antimalarial drugs. X-ray powder diffraction has established that the unit cell contains a cyclic hematin dimer, yet the pro-chiral nature of heme supports formation of four distinct stereoisomers, two centrosymmetric and two chiral enantiomers. Here we apply emerging methods of in situ cryo-electron tomography and diffraction to obtain a definitive structure of biogenic hemozoin. Individual crystals take a striking polar morphology. Diffraction analysis, supported by density functional theory, indicates a compositional mixture of one centrosymmetric and one chiral dimer, whose absolute configuration has been determined on the basis of crystal morphology and interaction with the aqueous medium. Structural modeling of the heme detoxification protein suggests a mechanism for dimer selection. The refined structure of hemozoin should serve as a guide to new drug development.</jats:p>

Topics

• density
• impedance spectroscopy
• morphology
• theory
• electron diffraction
• tomography
• density functional theory
• crystallization