Engineering Pak1 Allosteric Switches.
Engineering Pak1 Allosteric Switches.
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DOI:
10.1021/acssynbio.6b00359
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发表时间:
2017-07-21
影响因子:
4.7
通讯作者:
Hahn KM
中科院分区:
文献类型:
--
作者:
Dagliyan O;Karginov AV;Yagishita S;Gale ME;Wang H;DerMardirossian C;Wells CM;Dokholyan NV;Kasai H;Hahn KM
p21-activated kinases (PAKs) are important regulators of cell motility and morphology. It has been challenging to interrogate their functions because cells adapt to genetic manipulation of PAK, and because inhibitors act on multiple PAK isoforms. Here we describe genetically encoded PAK1 analogues that can be selectively activated by the membrane-permeable small molecule rapamycin. An engineered domain inserted away from the active site responds to rapamycin to allosterically control activity of the PAK1 isoform. To examine the mechanism of rapamycin-induced PAK1 activation, we used molecular dynamics with graph theory to predict amino acids involved in allosteric communication with the active site. This analysis revealed allosteric pathways that were exploited to generate kinase switches. Activation of PAK1 resulted in transient cell spreading in metastatic breast cancer cells, and long-term dendritic spine enlargement in mouse hippocampal CA1 neurons.
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影响因子:
64.8
作者:
Hayashi-Takagi A;Yagishita S;Nakamura M;Shirai F;Wu YI;Loshbaugh AL;Kuhlman B;Hahn KM;Kasai H
通讯作者:
Kasai H
影响因子:
3.3
作者:
Shirvanyants, David;Ding, Feng;Tsao, Douglas;Ramachandran, Srinivas;Dokholyan, Nikolay V.
通讯作者:
Dokholyan, Nikolay V.
DOI:
10.1126/science.1159052
发表时间:
2008-10-17
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Lee J;Natarajan M;Nashine VC;Socolich M;Vo T;Russ WP;Benkovic SJ;Ranganathan R
通讯作者:
Ranganathan R
影响因子:
14.9
作者:
Simonetti FL;Teppa E;Chernomoretz A;Nielsen M;Marino Buslje C
通讯作者:
Marino Buslje C
DOI:
10.1126/science.aah3404
发表时间:
2016-12-16
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Dagliyan O;Tarnawski M;Chu PH;Shirvanyants D;Schlichting I;Dokholyan NV;Hahn KM
通讯作者:
Hahn KM