Suppr超能文献

提高 I 类磷脂酰肌醇 4,5-二磷酸 3-激酶的产量。

Improved production of class I phosphatidylinositol 4,5-bisphosphate 3-kinase.

机构信息

Protein Expression Laboratory, NCI RAS Initiative, Frederick National Laboratory for Cancer Research, Frederick, MD, 21702, USA.

Protein Expression Laboratory, NCI RAS Initiative, Frederick National Laboratory for Cancer Research, Frederick, MD, 21702, USA.

出版信息

Protein Expr Purif. 2025 Jan;225:106582. doi: 10.1016/j.pep.2024.106582. Epub 2024 Aug 20.

Abstract

Phosphatidylinositol 4,5-bisphosphate 3-kinases (PI3K) are a family of kinases whose activity affects pathways needed for basic cell functions. As a result, PI3K is one of the most mutated genes in all human cancers and serves as an ideal therapeutic target for cancer treatment. Expanding on work done by other groups we improved protein yield to produce stable and pure protein using a variety of modifications including improved solubility tag, novel expression modalities, and optimized purification protocol and buffer. By these means, we achieved a 40-fold increase in yield for p110α/p85α and a 3-fold increase in p110α. We also used these protocols to produce comparable constructs of the β and δ isoforms of PI3K. Increased yield enhanced the efficiency of our downstream high throughput drug discovery efforts on the PIK3 family of kinases.

摘要

磷脂酰肌醇 4,5-二磷酸 3-激酶(PI3K)是一组激酶,其活性影响基本细胞功能所需的途径。因此,PI3K 是所有人类癌症中突变最多的基因之一,是癌症治疗的理想治疗靶点。在其他小组工作的基础上,我们通过各种修饰(包括改进的可溶性标签、新的表达方式以及优化的纯化方案和缓冲液)来提高蛋白质产量,以产生稳定和纯的蛋白质。通过这些方法,我们使 p110α/p85α 的产量增加了 40 倍,p110α 的产量增加了 3 倍。我们还使用这些方案来生产 PI3K 的β和δ同工型的可比构建体。产量的增加提高了我们在 PIK3 激酶家族下游高通量药物发现工作的效率。

相似文献

1
Improved production of class I phosphatidylinositol 4,5-bisphosphate 3-kinase.
Protein Expr Purif. 2025 Jan;225:106582. doi: 10.1016/j.pep.2024.106582. Epub 2024 Aug 20.
2
p110α and p110β isoforms of PI3K are involved in protection against HO induced oxidative stress in cancer cells.
Breast Cancer. 2019 May;26(3):378-385. doi: 10.1007/s12282-018-0933-x. Epub 2018 Nov 29.
4
Molecular mechanism of activation of class IA phosphoinositide 3-kinases (PI3Ks) by membrane-localized HRas.
J Biol Chem. 2017 Jul 21;292(29):12256-12266. doi: 10.1074/jbc.M117.789263. Epub 2017 May 17.
5
Regulation of lipid binding underlies the activation mechanism of class IA PI3-kinases.
Oncogene. 2012 Aug 9;31(32):3655-66. doi: 10.1038/onc.2011.532. Epub 2011 Nov 28.
6
Defining How Oncogenic and Developmental Mutations of PIK3R1 Alter the Regulation of Class IA Phosphoinositide 3-Kinases.
Structure. 2020 Feb 4;28(2):145-156.e5. doi: 10.1016/j.str.2019.11.013. Epub 2019 Dec 9.
7
Double mutations in cis increase oncogenicity and sensitivity to PI3Kα inhibitors.
Science. 2019 Nov 8;366(6466):714-723. doi: 10.1126/science.aaw9032.
8
PIK3CA C-terminal frameshift mutations are novel oncogenic events that sensitize tumors to PI3K-α inhibition.
Proc Natl Acad Sci U S A. 2020 Sep 29;117(39):24427-24433. doi: 10.1073/pnas.2000060117. Epub 2020 Sep 14.
10
Class IA Phosphatidylinositol 3-Kinase Isoform p110α Mediates Vascular Remodeling.
Arterioscler Thromb Vasc Biol. 2015 Jun;35(6):1434-44. doi: 10.1161/ATVBAHA.114.304887. Epub 2015 Apr 23.

引用本文的文献

本文引用的文献

1
Adapting recombinant bacterial alkaline phosphatase for nucleotide exchange of small GTPases.
Protein Expr Purif. 2024 Jun;218:106446. doi: 10.1016/j.pep.2024.106446. Epub 2024 Feb 22.
2
Class I PI3K Biology.
Curr Top Microbiol Immunol. 2022;436:3-49. doi: 10.1007/978-3-031-06566-8_1.
4
Cryo-EM structures of PI3Kα reveal conformational changes during inhibition and activation.
Proc Natl Acad Sci U S A. 2021 Nov 9;118(45). doi: 10.1073/pnas.2109327118.
5
Author Correction: PI3K inhibitors are finally coming of age.
Nat Rev Drug Discov. 2021 Oct;20(10):798. doi: 10.1038/s41573-021-00300-7.
6
Homogeneous Dual-Parametric-Coupled Assay for Simultaneous Nucleotide Exchange and KRAS/RAF-RBD Interaction Monitoring.
Anal Chem. 2020 Apr 7;92(7):4971-4979. doi: 10.1021/acs.analchem.9b05126. Epub 2020 Mar 9.
7
Targeting PI3K signaling in cancer: Challenges and advances.
Biochim Biophys Acta Rev Cancer. 2019 Apr;1871(2):361-366. doi: 10.1016/j.bbcan.2019.03.003. Epub 2019 Apr 1.
8
Structural Determinants of Isoform Selectivity in PI3K Inhibitors.
Biomolecules. 2019 Feb 26;9(3):82. doi: 10.3390/biom9030082.
10
Isoform-specific activities of the regulatory subunits of phosphatidylinositol 3-kinases - potentially novel therapeutic targets.
Expert Opin Ther Targets. 2018 Oct;22(10):869-877. doi: 10.1080/14728222.2018.1522302. Epub 2018 Sep 24.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验