Theoretical Soft Matter and Biophysics, Institute of Complex Systems and Institute for Advanced Simulation, Forschungszentrum Jülich, Jülich, Germany.
Theoretical Soft Matter and Biophysics, Institute of Complex Systems and Institute for Advanced Simulation, Forschungszentrum Jülich, Jülich, Germany.
Biophys J. 2019 Oct 1;117(7):1202-1214. doi: 10.1016/j.bpj.2019.08.027. Epub 2019 Aug 29.
Invasion of erythrocytes by merozoites is an essential step for the survival and progression of malaria parasites. To invade red blood cells (RBCs), apicomplexan parasites have to adhere with their apex to the RBC membrane. This necessary apex-membrane contact (or alignment) is not immediately established because the orientation of a free merozoite with respect to the RBC membrane is random when an adhesion contact first occurs. Therefore, it has been suggested that after the initial adhesion, merozoites facilitate their proper alignment by inducing considerable membrane deformations, frequently observed before the invasion process. This proposition is based on a positive correlation between RBC membrane deformation and successful invasion; however, the role of RBC mechanics and its deformation in the alignment process remains elusive. Using a mechanically realistic model of a deformable RBC, we investigate numerically the importance of RBC deformability for merozoite alignment. Adhesion between the parasite and RBC membrane is modeled by an attractive potential that might be inhomogeneous, mimicking possible adhesion gradients at the surface of a parasite. Our results show that RBC membrane deformations are crucial for successful merozoite alignment and require interaction strengths comparable to adhesion forces measured experimentally. Adhesion gradients along the parasite body further improve its alignment. Finally, an increased membrane rigidity is found to result in poor merozoite alignment, which can be a possible reason for a reduction in the invasion susceptibility of RBCs in several blood diseases associated with membrane stiffening.
疟原虫裂殖子入侵红细胞是疟原虫生存和发展的关键步骤。为了入侵红细胞(RBC), 顶复门寄生虫必须用它们的顶端与 RBC 膜黏附。这种必要的顶端-膜接触(或对准)不会立即建立,因为当首次发生黏附接触时,自由裂殖子相对于 RBC 膜的方向是随机的。因此,有人提出,在初始黏附之后,裂殖子通过诱导相当大的膜变形来促进它们的正确对准,这种变形通常在入侵过程之前观察到。这一假设基于 RBC 膜变形与成功入侵之间的正相关;然而,RBC 力学及其在对准过程中的变形的作用仍然难以捉摸。我们使用可变形 RBC 的力学上逼真的模型来数值研究 RBC 可变形性对裂殖子对准的重要性。寄生虫和 RBC 膜之间的黏附通过可能不均匀的吸引力势来建模,模拟寄生虫表面可能存在的黏附梯度。我们的结果表明,RBC 膜变形对于成功的裂殖子对准至关重要,并且需要与实验测量的黏附力相当的相互作用强度。沿寄生虫体的黏附梯度进一步改善了其对准。最后,发现增加的膜刚性会导致裂殖子对准不良,这可能是几种与膜变硬相关的血液疾病中 RBC 入侵敏感性降低的一个可能原因。