School of Chemistry and Biochemistry, NCCR Chemical Biology, University of Geneva, 1211, Geneva, Switzerland.
Chembiochem. 2022 Aug 3;23(15):e202200192. doi: 10.1002/cbic.202200192. Epub 2022 May 24.
Labeled ammonium cations with pK ∼7.4 accumulate in acidic organelles because they can be neutralized transiently to cross the membrane at cytosolic pH 7.2 but not at their internal pH<5.5. Retention in early endosomes with less acidic internal pH was achieved recently using weaker acids of up to pK 9.8. We report here that primary ammonium cations with higher pK 10.6, label early endosomes more efficiently. This maximized early endosome tracking coincides with increasing labeling of Golgi networks with similarly weak internal acidity. Guanidinium cations with pK 13.5 cannot cross the plasma membrane in monomeric form and label the plasma membrane with selectivity for vesicles embarking into endocytosis. Self-assembled into micelles, guanidinium cations enter cells like arginine-rich cell-penetrating peptides and, driven by their membrane potential, penetrate mitochondria unidirectionally despite their high inner pH. The resulting tracking rules with an approximated dynamic range of pK change ∼3.5 are expected to be generally valid, thus enabling the design of chemistry tools for biology research in the broadest sense. From a practical point of view, most relevant are two complementary fluorescent flipper probes that can be used to image the mechanics at the very beginning of endocytosis.
标记的 pK∼7.4 的铵阳离子在酸性细胞器中积累,因为它们可以在细胞质 pH7.2 时被暂时中和以穿过膜,但不能在内部 pH<5.5 时穿过。最近使用 pK 值高达 9.8 的较弱酸在早期内涵体中实现了保留。我们在这里报告,pK10.6 更高的伯铵阳离子更有效地标记早期内涵体。这种最大程度的早期内涵体跟踪与用类似弱内部酸度进行的高尔基体网络的增加标记相吻合。pK13.5 的胍阳离子不能以单体形式穿过质膜,并选择性地标记质膜上进入胞吞作用的囊泡。胍阳离子自组装成胶束,以类似于富含精氨酸的细胞穿透肽的方式进入细胞,并且由于它们的膜电位,尽管它们的内部 pH 值很高,也可以单向穿透线粒体。这些跟踪规则具有约 pK 变化的动态范围为 3.5,预计将具有普遍的有效性,从而能够设计用于生物学研究的化学工具。从实际的角度来看,最重要的是两种互补的荧光翻转探针,可用于成像胞吞作用开始时的力学。