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本文引用的文献

1
A homozygous missense variant in with early-onset Crohn's disease, growth failure and dysmorphic features in an infant: a case report.携带有早发性克罗恩病、生长发育迟缓及先天畸形特征的纯合错义变异:一例病例报告。
J Genet. 2023;102.
2
The first association study of Protein Tyrosine Phosphatase, Non-Receptor Type 2 (PTPN2) gene polymorphisms in Malaysian patients with Crohn's disease.马来西亚克罗恩病患者蛋白酪氨酸磷酸酶非受体型 2(PTPN2)基因多态性的首次关联研究。
Gene. 2022 Aug 20;836:146661. doi: 10.1016/j.gene.2022.146661. Epub 2022 Jun 6.
3
The Inhibitors of Protein Tyrosine Phosphatase Nonreceptor Type 2 (PTPN2) as Potential Enhancers of Cancer Immunotherapy and Type 1 (PTPN1) as Treatment of Metabolic Diseases.蛋白酪氨酸磷酸酶非受体2型(PTPN2)抑制剂作为癌症免疫治疗的潜在增强剂以及蛋白酪氨酸磷酸酶非受体1型(PTPN1)抑制剂作为代谢性疾病的治疗方法。
ACS Med Chem Lett. 2021 Dec 27;13(1):19-21. doi: 10.1021/acsmedchemlett.1c00678. eCollection 2022 Jan 13.
4
Crystal Structure of TCPTP Unravels an Allosteric Regulatory Role of Helix α7 in Phosphatase Activity.非受体型蛋白酪氨酸磷酸酶TCPTP的晶体结构揭示了α7螺旋在磷酸酶活性中的变构调节作用
Biochemistry. 2021 Dec 28;60(51):3856-3867. doi: 10.1021/acs.biochem.1c00519. Epub 2021 Dec 15.
5
Structural characterization of a pathogenic mutant of human protein tyrosine phosphatase PTPN2 (Cys216Gly) that causes very early onset autoimmune enteropathy.一种导致非常早发性自身免疫性肠病的人蛋白酪氨酸磷酸酶 PTPN2(半胱氨酸 216 甘氨酸)致病性突变体的结构特征。
Protein Sci. 2022 Feb;31(2):538-544. doi: 10.1002/pro.4246. Epub 2021 Nov 27.
6
PTP1B Is an Intracellular Checkpoint that Limits T-cell and CAR T-cell Antitumor Immunity.PTP1B 是一种细胞内检查点,限制 T 细胞和 CAR T 细胞抗肿瘤免疫。
Cancer Discov. 2022 Mar 1;12(3):752-773. doi: 10.1158/2159-8290.CD-21-0694.
7
PTPN2 Deficiency Enhances Programmed T Cell Expansion and Survival Capacity of Activated T Cells.PTPN2 缺乏增强了活化 T 细胞的程序性细胞增殖和存活能力。
Cell Rep. 2020 Jul 28;32(4):107957. doi: 10.1016/j.celrep.2020.107957.
8
Loss-of-Function Mutation in PTPN2 Causes Aberrant Activation of JAK Signaling Via STAT and Very Early Onset Intestinal Inflammation.PTPN2功能丧失突变通过STAT导致JAK信号异常激活及极早发性肠道炎症。
Gastroenterology. 2020 Nov;159(5):1968-1971.e4. doi: 10.1053/j.gastro.2020.07.040. Epub 2020 Jul 25.
9
PTPN2 phosphatase deletion in T cells promotes anti-tumour immunity and CAR T-cell efficacy in solid tumours.T 细胞中 PTPN2 磷酸酶缺失可促进实体瘤中的抗肿瘤免疫和 CAR T 细胞疗效。
EMBO J. 2020 Jan 15;39(2):e103637. doi: 10.15252/embj.2019103637. Epub 2019 Dec 5.
10
T-Cell-Specific PTPN2 Deficiency in NOD Mice Accelerates the Development of Type 1 Diabetes and Autoimmune Comorbidities.NOD 小鼠 T 细胞特异性 PTPN2 缺乏加速 1 型糖尿病和自身免疫合并症的发展。
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通过抑制剂可及结合位点增强载脂蛋白酪氨酸磷酸酶非受体型 2 的晶体浸泡策略。

Enhancing the apo protein tyrosine phosphatase non-receptor type 2 crystal soaking strategy through inhibitor-accessible binding sites.

机构信息

Pfizer Boulder Research and Development, Boulder, CO 80301, USA.

出版信息

Acta Crystallogr F Struct Biol Commun. 2024 Sep 1;80(Pt 9):210-219. doi: 10.1107/S2053230X24007866. Epub 2024 Aug 23.

DOI:10.1107/S2053230X24007866
PMID:39177701
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11376276/
Abstract

Protein tyrosine phosphatase non-receptor type 2 (PTPN2) has recently been recognized as a promising target for cancer immunotherapy. Despite extensive structural and functional studies of other protein tyrosine phosphatases, there is limited structural understanding of PTPN2. Currently, there are only five published PTPN2 structures and none are truly unbound due to the presence of a mutation, an inhibitor or a loop (related to crystal packing) in the active site. In this report, a novel crystal packing is revealed that resulted in a true apo PTPN2 crystal structure with an unbound active site, allowing the active site to be observed in a native apo state for the first time. Key residues related to accommodation in the active site became identifiable upon comparison with previously published PTPN2 structures. Structures of PTPN2 in complex with an established PTPN1 active-site inhibitor and an allosteric inhibitor were achieved through soaking experiments using these apo PTPN2 crystals. The increased structural understanding of apo PTPN2 and the ability to soak in inhibitors will aid the development of future PTPN2 inhibitors.

摘要

蛋白酪氨酸磷酸酶非受体型 2(PTPN2)最近被认为是癌症免疫治疗的一个有前途的靶点。尽管对其他蛋白酪氨酸磷酸酶进行了广泛的结构和功能研究,但对 PTPN2 的结构了解有限。目前,仅发表了五篇 PTPN2 结构的论文,由于活性位点存在突变、抑制剂或环(与晶体包装有关),没有真正的无结合物结构。在本报告中,揭示了一种新的晶体包装,导致了一个真正的无结合物 PTPN2 晶体结构,具有未结合的活性位点,首次使活性位点能够以天然的无结合物状态被观察到。通过与先前发表的 PTPN2 结构进行比较,可以识别与活性位点容纳相关的关键残基。通过使用这些无结合物 PTPN2 晶体进行浸泡实验,实现了 PTPN2 与已建立的 PTPN1 活性位点抑制剂和别构抑制剂的复合物结构。对 apo PTPN2 的结构理解的增加以及能够浸泡抑制剂将有助于未来 PTPN2 抑制剂的开发。