• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

脂质包被的蛋白质凝聚物作为具有对生物分子选择性摄取能力的稳定原始细胞。

Lipid coated protein condensates as stable protocells with selective uptake abilities for biomolecules.

作者信息

Son Juyoung, Jung Yongwon

机构信息

Department of Chemistry, KAIST 291 Daehak-ro, Yuseong-gu Daejeon 34141 Republic of Korea

出版信息

Chem Sci. 2022 Sep 27;13(40):11841-11848. doi: 10.1039/d2sc03123j. eCollection 2022 Oct 19.

DOI:10.1039/d2sc03123j
PMID:36320904
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9580490/
Abstract

To create cell-like synthetic systems, spatial confinement that is stable against environmental changes and selective uptake of diverse biomolecules into these compartments are key initial conditions. However, fabrication of protocells with these two features has been extremely difficult. Here, we used fully protein-based liquid condensates and a lipid coating on these condensates to construct highly stable protocells with an uptake ability for outside biomolecules. Condensates with an extremely high density of 6His-tagged proteins were coated with Ni(ii)-NTA(nitrilotriacetic acid)-modified lipids. High condensate rigidity and specific 6His-Ni-NTA interactions enabled the formation of lipid-protein protocells, which are stable even after centrifugations. In addition, immobile lipid coatings on condensates were permeable to outside biomolecules. When binding modules were fused into condensate-forming proteins, the resulting functionalized condensate-protocells could strongly and selectively uptake various outside proteins through specific protein interactions.

摘要

为了创建类似细胞的合成系统,对环境变化具有稳定性的空间限制以及将多种生物分子选择性摄取到这些隔室中是关键的初始条件。然而,制造具有这两个特征的原始细胞极其困难。在这里,我们使用完全基于蛋白质的液体凝聚物以及这些凝聚物上的脂质涂层来构建对外部生物分子具有摄取能力的高度稳定的原始细胞。用镍(II)-氮川三乙酸(NTA)修饰的脂质包裹具有极高密度的6His标签蛋白的凝聚物。高凝聚物刚性和特定的6His-Ni-NTA相互作用使得脂质-蛋白质原始细胞得以形成,即使经过离心处理它们也很稳定。此外,凝聚物上固定的脂质涂层对外部生物分子具有渗透性。当将结合模块融合到形成凝聚物的蛋白质中时,由此产生的功能化凝聚物-原始细胞可以通过特定的蛋白质相互作用强烈且选择性地摄取各种外部蛋白质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e8c/9580490/fba41d8efcfa/d2sc03123j-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e8c/9580490/a41f2b7a383d/d2sc03123j-s1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e8c/9580490/08ee5c67f015/d2sc03123j-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e8c/9580490/d80d510a2dc1/d2sc03123j-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e8c/9580490/191c8dbed918/d2sc03123j-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e8c/9580490/fba41d8efcfa/d2sc03123j-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e8c/9580490/a41f2b7a383d/d2sc03123j-s1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e8c/9580490/08ee5c67f015/d2sc03123j-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e8c/9580490/d80d510a2dc1/d2sc03123j-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e8c/9580490/191c8dbed918/d2sc03123j-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e8c/9580490/fba41d8efcfa/d2sc03123j-f4.jpg

相似文献

1
Lipid coated protein condensates as stable protocells with selective uptake abilities for biomolecules.脂质包被的蛋白质凝聚物作为具有对生物分子选择性摄取能力的稳定原始细胞。
Chem Sci. 2022 Sep 27;13(40):11841-11848. doi: 10.1039/d2sc03123j. eCollection 2022 Oct 19.
2
Valency and Binding Affinity Variations Can Regulate the Multilayered Organization of Protein Condensates with Many Components.配体价和结合亲和力的变化可以调节具有多种成分的蛋白质凝聚物的多层组织。
Biomolecules. 2021 Feb 14;11(2):278. doi: 10.3390/biom11020278.
3
Incorporation and Assembly of a Light-Emitting Enzymatic Reaction into Model Protein Condensates.将发光酶反应纳入模型蛋白凝聚体中。
Biochemistry. 2021 Oct 26;60(42):3137-3151. doi: 10.1021/acs.biochem.1c00373. Epub 2021 Oct 14.
4
Development and characterization of Ni-NTA-bearing microspheres.含镍-氮三乙酸微球的制备与表征
Cytometry. 2002 Jul 1;48(3):136-45. doi: 10.1002/cyto.10124.
5
Lipid Membrane Topographies Are Regulators for the Spatial Distribution of Liquid Protein Condensates.脂膜形貌是液-液相分离蛋白凝聚体空间分布的调控者。
Nano Lett. 2024 Apr 17;24(15):4330-4335. doi: 10.1021/acs.nanolett.3c04169. Epub 2024 Apr 5.
6
Biomolecular condensates modulate membrane lipid packing and hydration.生物分子凝聚物调节膜脂的堆积和水合作用。
Nat Commun. 2023 Sep 28;14(1):6081. doi: 10.1038/s41467-023-41709-5.
7
Behavior control of membrane-less protein liquid condensates with metal ion-induced phase separation.无膜蛋白液滴的金属离子诱导相分离行为控制。
Nat Commun. 2020 Nov 3;11(1):5554. doi: 10.1038/s41467-020-19391-8.
8
Protein Condensate Atlas from predictive models of heteromolecular condensate composition.蛋白质凝聚物图谱来自异源凝聚物组成的预测模型。
Nat Commun. 2024 Jul 10;15(1):5418. doi: 10.1038/s41467-024-48496-7.
9
Kinetic interplay between droplet maturation and coalescence modulates shape of aged protein condensates.液滴成熟和聚结之间的动力学相互作用调节了老化蛋白质凝聚体的形状。
Sci Rep. 2022 Mar 15;12(1):4390. doi: 10.1038/s41598-022-08130-2.
10
ALS-linked mutations impair UBQLN2 stress-induced biomolecular condensate assembly in cells.ALS 相关突变会损害 UBQLN2 在细胞中应激诱导的生物分子凝聚物的组装。
J Neurochem. 2021 Oct;159(1):145-155. doi: 10.1111/jnc.15453. Epub 2021 Aug 20.

引用本文的文献

1
Polymeric and Polymer-Functionalized Drug Delivery Vectors: From Molecular Architecture and Elasticity to Cellular Uptake.聚合物及聚合物功能化药物递送载体:从分子结构与弹性到细胞摄取
Polymers (Basel). 2025 Aug 19;17(16):2243. doi: 10.3390/polym17162243.
2
Active Armoring of Protocell Condensates with Metal-Phenolic Networks.利用金属酚醛网络对原细胞凝聚物进行主动装甲防护。
Small. 2025 May 12:e2503077. doi: 10.1002/smll.202503077.
3
Size-controlled assembly of phase separated protein condensates with interfacial protein cages.具有界面蛋白笼的相分离蛋白凝聚物的尺寸控制组装

本文引用的文献

1
Synthesis of lipid membranes for artificial cells.用于人造细胞的脂质膜合成。
Nat Rev Chem. 2021 Oct;5(10):676-694. doi: 10.1038/s41570-021-00303-3. Epub 2021 Jul 19.
2
Synthetic Cells: From Simple Bio-Inspired Modules to Sophisticated Integrated Systems.人工合成细胞:从简单的仿生模块到复杂的集成系统。
Angew Chem Int Ed Engl. 2022 Apr 11;61(16):e202110855. doi: 10.1002/anie.202110855. Epub 2022 Mar 30.
3
Regulation of biomolecular condensates by interfacial protein clusters.界面蛋白簇对生物分子凝聚物的调控。
Nat Commun. 2025 Jan 25;16(1):1009. doi: 10.1038/s41467-025-56391-y.
4
Multicompartmental coacervate-based protocell by spontaneous droplet evaporation.自发液滴蒸发法制备多隔室凝聚体原代细胞。
Nat Commun. 2024 Feb 6;15(1):1107. doi: 10.1038/s41467-024-45411-y.
5
Tuning the viscoelastic properties of peptide coacervates by single amino acid mutations and salt kosmotropicity.通过单氨基酸突变和盐的促溶能力调节肽凝聚层的粘弹性特性。
Commun Chem. 2024 Jan 4;7(1):5. doi: 10.1038/s42004-023-01094-y.
Science. 2021 Sep 10;373(6560):1218-1224. doi: 10.1126/science.abg7071. Epub 2021 Sep 9.
4
Synthetic tissue engineering with smart, cytomimetic protocells.智能仿生原代细胞的组织工程合成
Biomaterials. 2021 Sep;276:120941. doi: 10.1016/j.biomaterials.2021.120941. Epub 2021 Jun 28.
5
Interplay between intrinsically disordered proteins inside membraneless protein liquid droplets.无膜蛋白液滴内内在无序蛋白之间的相互作用。
Chem Sci. 2019 Dec 11;11(5):1269-1275. doi: 10.1039/c9sc03191j.
6
Membranization of Coacervates into Artificial Phagocytes with Predation toward Bacteria.凝聚体膜化成具有细菌吞噬作用的人工吞噬细胞。
ACS Nano. 2021 Jun 22;15(6):10048-10057. doi: 10.1021/acsnano.1c01694. Epub 2021 May 28.
7
Giant Coacervate Vesicles As an Integrated Approach to Cytomimetic Modeling.巨凝聚体囊泡作为一种细胞模拟的综合方法。
J Am Chem Soc. 2021 Feb 24;143(7):2866-2874. doi: 10.1021/jacs.0c12494. Epub 2021 Feb 10.
8
Programmed spatial organization of biomacromolecules into discrete, coacervate-based protocells.将生物大分子编程为离散的、凝聚物为基础的原细胞。
Nat Commun. 2020 Dec 8;11(1):6282. doi: 10.1038/s41467-020-20124-0.
9
Enzyme-mediated nitric oxide production in vasoactive erythrocyte membrane-enclosed coacervate protocells.酶介导的活性红细胞膜包被凝聚体原细胞中一氧化氮的产生。
Nat Chem. 2020 Dec;12(12):1165-1173. doi: 10.1038/s41557-020-00585-y. Epub 2020 Nov 20.
10
Cellular Control of Viscosity Counters Changes in Temperature and Energy Availability.细胞控制黏度以应对温度和能量供应的变化。
Cell. 2020 Dec 10;183(6):1572-1585.e16. doi: 10.1016/j.cell.2020.10.017. Epub 2020 Nov 5.