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分支与线性 Arp2/3 生成的肌动蛋白丝的调节。

Regulation of branched versus linear Arp2/3-generated actin filaments.

机构信息

Université Paris Cité, CNRS, Institut Jacques Monod, Paris, France.

The Francis Crick Institute, London, UK.

出版信息

EMBO J. 2023 May 2;42(9):e113008. doi: 10.15252/embj.2022113008. Epub 2023 Mar 20.

Abstract

Activation of the Arp2/3 complex by VCA-motif-bearing actin nucleation-promoting factors results in the formation of "daughter" actin filaments branching off the sides of pre-existing "mother" filaments. Alternatively, when stimulated by SPIN90, Arp2/3 directly nucleates "linear" actin filaments. Uncovering the similarities and differences between these two mechanisms is fundamental to understanding how actin cytoskeleton dynamics are regulated. Here, analysis of individual filaments reveals that, unexpectedly, the VCA motifs of WASP, N-WASP, and WASH destabilize existing branches, as well as SPIN90-Arp2/3 at linear filament ends. Furthermore, branch stabilizer cortactin and destabilizer GMF each have a similar impact on SPIN90-activated Arp2/3. However, unlike branch junctions, SPIN90-Arp2/3 at the ends of linear filaments is not destabilized by piconewton forces and does not become less stable with time. It thus appears that linear and branched Arp2/3-generated filaments respond similarly to the regulatory proteins we have tested, albeit with some differences, but significantly differ in their responses to aging and mechanical stress. These kinetic differences likely reflect the small conformational differences recently reported between Arp2/3 in branch junctions and linear filaments and suggest that their turnover in cells may be differently regulated.

摘要

Arp2/3 复合物被 VCA 基序结合的成核促进因子激活,导致“子”肌动蛋白丝从预先存在的“母”丝的侧面分支出来。或者,当被 SPIN90 刺激时,Arp2/3 直接引发“线性”肌动蛋白丝。揭示这两种机制之间的相似性和差异性对于理解肌动蛋白细胞骨架动力学的调节至关重要。在这里,对单个纤维丝的分析表明,出乎意料的是,WASP、N-WASP 和 WASH 的 VCA 基序不仅会使 SPIN90-Arp2/3 在线性纤维丝末端稳定分支,还会使现有分支失稳。此外,分支稳定剂 cortactin 和去稳定剂 GMF 对 SPIN90 激活的 Arp2/3 都有类似的影响。然而,与分支连接点不同,线性纤维丝末端的 SPIN90-Arp2/3 不会被皮牛顿力去稳定化,并且不会随着时间的推移变得不稳定。因此,似乎线性和分支的 Arp2/3 生成的纤维丝对我们已经测试的调节蛋白的反应相似,尽管存在一些差异,但它们对老化和机械应激的反应明显不同。这些动力学差异可能反映了最近报道的分支连接点和线性纤维丝之间的 Arp2/3 之间的小构象差异,并表明它们在细胞中的周转率可能受到不同的调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9edc/10152144/53e54af49c17/EMBJ-42-e113008-g004.jpg

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