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被困住了!对测量总细胞摄取与胞质定位方法的批判性评估。

Trapped! A Critical Evaluation of Methods for Measuring Total Cellular Uptake versus Cytosolic Localization.

机构信息

Department of Chemistry , Tufts University , 62 Talbot Avenue , Medford , Massachusetts 02155 , United States.

Department of Biochemistry , University of Zurich , Winterthurerstrasse 190 , 8057 Zurich , Switzerland.

出版信息

Bioconjug Chem. 2019 Apr 17;30(4):1006-1027. doi: 10.1021/acs.bioconjchem.9b00112. Epub 2019 Apr 5.

Abstract

Biomolecules have many properties that make them promising for intracellular therapeutic applications, but delivery remains a key challenge because large biomolecules cannot easily enter the cytosol. Furthermore, quantification of total intracellular versus cytosolic concentrations remains demanding, and the determination of delivery efficiency is thus not straightforward. In this review, we discuss strategies for delivering biomolecules into the cytosol and briefly summarize the mechanisms of uptake for these systems. We then describe commonly used methods to measure total cellular uptake and, more selectively, cytosolic localization, and discuss the major advantages and drawbacks of each method. We critically evaluate methods of measuring "cell penetration" that do not adequately distinguish total cellular uptake and cytosolic localization, which often lead to inaccurate interpretations of a molecule's cytosolic localization. Finally, we summarize the properties and components of each method, including the main caveats of each, to allow for informed decisions about method selection for specific applications. When applied correctly and interpreted carefully, methods for quantifying cytosolic localization offer valuable insight into the bioactivity of biomolecules and potentially the prospects for their eventual development into therapeutics.

摘要

生物分子具有许多特性,使其成为细胞内治疗应用的有前途的候选物,但输送仍然是一个关键挑战,因为大型生物分子不容易进入细胞质。此外,定量测定细胞内与细胞质中的总浓度仍然具有挑战性,因此输送效率的确定并不简单。在这篇综述中,我们讨论了将生物分子递送到细胞质中的策略,并简要总结了这些系统的摄取机制。然后,我们描述了常用的测量总细胞摄取的方法,以及更有选择性的细胞质定位的方法,并讨论了每种方法的主要优点和缺点。我们批判性地评估了那些不能充分区分总细胞摄取和细胞质定位的“细胞穿透”测量方法,这些方法常常导致对分子细胞质定位的不准确解释。最后,我们总结了每种方法的特性和组成部分,包括每种方法的主要注意事项,以便为特定应用的方法选择提供信息。当正确应用和仔细解释时,定量测定细胞质定位的方法可以为生物分子的生物活性提供有价值的见解,并有可能为它们最终开发为治疗药物提供前景。

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