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衔接蛋白输入蛋白α以效率为代价提供了对核输入的灵活控制。

The adapter importin-alpha provides flexible control of nuclear import at the expense of efficiency.

作者信息

Riddick Greg, Macara Ian G

机构信息

Department of Biochemistry, University of Virginia, Charlottesville, VA 22908, USA.

出版信息

Mol Syst Biol. 2007;3:118. doi: 10.1038/msb4100160. Epub 2007 Jun 5.

Abstract

Although there exists a large family of nuclear transport receptors (Karyopherins), the majority of known import cargoes use an adapter protein, Importin-alpha (Impalpha), which links the cargo to a karyopherin, Importin-beta (Impbeta). The reason for the existence of transport adapters is unknown. One hypothesis is that, as Impalpha re-export is coupled to GTP hydrolysis, it can drive a higher concentration of nuclear cargo than could be achieved by direct cargo binding to Importin-beta. However, computer simulations predicted the opposite outcome, and showed that direct transport is faster than adapter-mediated transport. These predictions were validated experimentally. The data, together with previous analyses of nuclear protein import, suggest that the use of adapters such as importin-alpha provides the cell with increased dynamic range for control of nuclear import rates, but at the expense of efficiency.

摘要

尽管存在一大类核转运受体(核转运蛋白),但大多数已知的输入货物使用一种衔接蛋白,即输入蛋白α(Impα),它将货物连接到一种核转运蛋白,输入蛋白β(Impβ)。转运衔接蛋白存在的原因尚不清楚。一种假说认为,由于Impα的再输出与GTP水解偶联,它能够驱动比货物直接与输入蛋白β结合所能达到的更高浓度的核货物。然而,计算机模拟预测了相反的结果,并表明直接转运比衔接蛋白介导的转运更快。这些预测通过实验得到了验证。这些数据,连同先前对核蛋白输入的分析,表明使用诸如输入蛋白α这样的衔接蛋白为细胞提供了更大的动态范围来控制核输入速率,但以效率为代价。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47a1/1911202/7b3599c4af3c/msb4100160-f1.jpg

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