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血浆屏障背后的合成蛋白:分子间谍。

Synthetic Proteins behind the Plasma Barrier: Molecular Spies.

机构信息

Schulich Faculty of Chemistry, Technion-Israel Institute of Technology, Haifa 3200008, Israel.

出版信息

Acc Chem Res. 2022 Aug 2;55(15):2055-2067. doi: 10.1021/acs.accounts.2c00236. Epub 2022 Jul 14.

DOI:10.1021/acs.accounts.2c00236
PMID:35833291
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9352316/
Abstract

There is a continuous demand to improve our understanding of fundamental processes that underlie human health and disease. Therefore, novel strategies that can assist in these efforts are required. For example, molecular biology and genetic approaches have revolutionized our understanding of protein-mediated processes by facilitating their direct visualization and analyses in living cells. Despite these developments, genetic manipulation has limitations in controlling events that occur after translation such as posttranslational modifications (PTMs), which are imperative regulatory elements. As a result, developing new methods to study PTMs in live cells is a major bottleneck in deciphering their exact roles in the myriad cellular processes.Synthetic and semisynthetic proteins are prepared by combining solid phase peptide synthesis (SPPS) and chemoselective ligation approaches with synthetic or recombinant peptides. Employing protein synthesis allows chemists to incorporate natural and unnatural modifications with virtually unlimited number of functional groups into the protein's sequence, such as PTMs and their mimics. In addition, synthetic proteins can include additional elements such as fluorescent tags, reactive groups, caged units, and enrichment handles. Therefore, harnessing the power of chemical protein synthesis offers great opportunities to study fundamental biological processes.Unfortunately, the low cell permeability of proteins limits their applications mainly to settings, excluding live cell studies. As a result, chemical biologists have been attempting to overcome these limitations by developing protein delivery methods that would enable the study of custom-made proteins in a biological context. Success with these strategies should enable accurate determination of protein localization, degradation, folding, interactions, and involvement in the assembly of membrane-less organelles formed by liquid-liquid phase separation inside cells. Importantly, protein delivery approaches are complementary to genetic manipulations, and combining these approaches should pave the way to new discoveries.In this Account, we describe recent developments in protein delivery methods, with emphasis on those most compatible with synthetic proteins. We highlight experimental approaches and conceptual adaptations required to design and study synthetic proteins in live cells, with or without genetic manipulation. In addition, we highlight the strength and weakness of these approaches for both the delivery and the subsequent studies. We also describe our endeavors to deliver synthetic proteins to cells via cell penetrating peptides (CPPs) and multiplexed bead loading (MBL), as showcases of the applications of these methods to shed light on biological processes. Lastly, we contemplate other future applications of synthetic proteins to answer questions that are currently unapproachable.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f571/9352316/b06b706e4d58/ar2c00236_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f571/9352316/3aa2099f4dd9/ar2c00236_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f571/9352316/d7aa186e53bb/ar2c00236_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f571/9352316/8cbb64d0070b/ar2c00236_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f571/9352316/a193219153c2/ar2c00236_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f571/9352316/5da9156c6194/ar2c00236_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f571/9352316/b5a7eb303960/ar2c00236_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f571/9352316/b06b706e4d58/ar2c00236_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f571/9352316/3aa2099f4dd9/ar2c00236_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f571/9352316/d7aa186e53bb/ar2c00236_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f571/9352316/8cbb64d0070b/ar2c00236_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f571/9352316/a193219153c2/ar2c00236_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f571/9352316/5da9156c6194/ar2c00236_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f571/9352316/b5a7eb303960/ar2c00236_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f571/9352316/b06b706e4d58/ar2c00236_0007.jpg
摘要

人们不断要求加深对人类健康和疾病相关基本过程的理解。因此,需要寻求新的策略来辅助实现这一目标。例如,分子生物学和遗传学方法通过直接在活细胞中可视化和分析蛋白质介导的过程,彻底改变了我们对这些过程的理解。尽管取得了这些进展,但遗传操作在控制翻译后事件方面存在局限性,例如翻译后修饰(PTMs),这些修饰是重要的调控元件。因此,开发新的方法来研究活细胞中的 PTM 是揭示其在众多细胞过程中确切作用的主要瓶颈。

通过将固相肽合成(SPPS)和化学选择性连接方法与合成或重组肽相结合,制备合成和半合成蛋白。采用蛋白质合成,化学家可以将天然和非天然修饰物及其类似物,以几乎无限数量的官能团,整合到蛋白质序列中,例如 PTM 及其类似物。此外,合成蛋白可以包含其他元件,例如荧光标记物、反应基团、笼状单元和富集处理单元。因此,利用化学蛋白质合成的力量为研究基本生物学过程提供了巨大的机会。

遗憾的是,由于蛋白质的细胞通透性低,限制了其应用主要局限于非活细胞环境,从而排除了活细胞研究。因此,化学生物学家一直试图通过开发蛋白递送来克服这些限制,从而能够在生物环境中研究定制蛋白。这些策略的成功应该能够准确确定蛋白质的定位、降解、折叠、相互作用以及在细胞内液-液相分离形成的无膜细胞器组装中的作用。重要的是,蛋白递送来方法与遗传操作互补,将这些方法相结合,应该能够为新发现铺平道路。

在本综述中,我们描述了蛋白递送方法的最新进展,重点介绍了与合成蛋白最兼容的方法。我们强调了设计和研究活细胞中合成蛋白所需的实验方法和概念调整,无论是否进行遗传操作。此外,我们还强调了这些方法在蛋白递送和后续研究中的优缺点。我们还描述了我们通过细胞穿透肽(CPP)和多重珠加载(MBL)将合成蛋白递送至细胞的努力,以此展示这些方法在阐明生物学过程中的应用。最后,我们考虑了合成蛋白在其他未来应用中回答目前无法解决的问题。

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