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BCC7 蛋白通过与 MyoC 马达和 IMC 膜网络之间的相互作用,有助于基极。

The BCC7 Protein Contributes to the Basal Pole by Interfacing between the MyoC Motor and the IMC Membrane Network.

机构信息

IAB, Team Biomechanics of Host-Apicomplexa Parasite, INSERM U1209, CNRS UMR5309, Grenoble Alpes University, 38700 Grenoble, France.

Université de Bordeaux, Team Microbiologie Fondamentale et Pathogénicité, CNRS UMR 5234, 33000 Bordeaux, France.

出版信息

Int J Mol Sci. 2022 May 26;23(11):5995. doi: 10.3390/ijms23115995.

DOI:10.3390/ijms23115995
PMID:35682673
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9181098/
Abstract

is a eukaryotic parasite that has evolved a stage called tachyzoite which multiplies in host cells by producing two daughter cells internally. These nascent tachyzoites bud off their mother and repeat the division process until the expanding progenies escape to settle and multiply in other host cells. Over these intra- and extra-cellular phases, the tachyzoite maintains an essential apicobasal polarity that emerges through a unique bidirectional budding process of the elongating cells. This process requires the assembly of several molecular complexes that, at the nascent pole, encompass structural and myosin motor elements. To characterize a recently identified basal pole marker named BCC7 with respect to the posterior myosin J and myosin C motors, we used conventional biochemistry as well as advanced proteomic and in silico analysis in conjunction with live and super resolution microscopy of transgenic fluorescent tachyzoites. We document that BCC7 forms a ribbed ring below which myosin C motor entities distribute regularly. In addition, we identified-among 13 BCC7 putative partners-two novel and five known members of the inner membrane complex (IMC) family which ends at the apical side of the ring. Therefore, BCC7 could assist the stabilization of the IMC plaques and contribute to the parasite biomechanical properties.

摘要

是一种真核寄生虫,它进化出了一个叫做速殖子的阶段,通过在宿主细胞内产生两个子细胞来进行繁殖。这些新生的速殖子从母细胞上脱落,并重复分裂过程,直到不断增殖的后代逸出,转移到其他宿主细胞中定居和繁殖。在这些细胞内和细胞间阶段,速殖子保持着一种基本的顶端-基底极性,这种极性是通过延长细胞的独特双向出芽过程产生的。这个过程需要组装几个分子复合物,在新生的顶端,这些复合物包含结构和肌球蛋白马达元件。为了研究最近鉴定的一个名为 BCC7 的基底极标记物与后向肌球蛋白 J 和肌球蛋白 C 马达的关系,我们使用了常规的生物化学以及先进的蛋白质组学和计算机分析,并结合了转荧光速殖子的活细胞和超分辨率显微镜技术。我们证明 BCC7 在肌球蛋白 C 马达实体有规则分布的下方形成一个有棱纹的环。此外,我们在 13 个 BCC7 的假定伙伴中鉴定出了两个新的和五个已知的内膜复合物 (IMC) 家族成员,这些成员在环的顶端终止。因此,BCC7 可以协助 IMC 斑块的稳定,并有助于寄生虫的生物力学特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb5a/9181098/b8762f98ee15/ijms-23-05995-g005.jpg
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