The Azrieli Faculty of Medicine in the Galilee, Bar-Ilan University, Safed 1311502, Israel.
Institute of Life Sciences, The Hebrew University of Jerusalem, Jerusalem 9190401, Israel.
Int J Mol Sci. 2022 May 28;23(11):6076. doi: 10.3390/ijms23116076.
Mitochondria play central roles in maintaining cellular metabolic homeostasis, cell survival and cell death, and generate most of the cell's energy. Mitochondria maintain their homeostasis by dynamic (fission and fusion) and quality control mechanisms, including mitophagy, the removal of damaged mitochondria that is mediated mainly by the Pink1/Parkin pathway. Pink1 is a serine/threonine kinase which regulates mitochondrial function, hitherto many molecular mechanisms underlying Pink1 activity in mitochondrial homeostasis and cell fate remain unknown. Peptides are vital biological mediators that demonstrate remarkable potency, selectivity, and low toxicity, yet they have two major limitations, low oral bioavailability and poor stability. Herein, we rationally designed a linear peptide that targets Pink1 and, using straightforward chemistry, we developed molecular probes with drug-like properties to further characterize Pink1. Initially, we conjugated a cell-penetrating peptide and a cross-linker to map Pink1's 3D structure and its interaction sites. Next, we conjugated a fluorescent dye for cell-imaging. Finally, we developed cyclic peptides with improved stability and binding affinity. Overall, we present a facile approach to converting a non-permeable linear peptide into a research tool possessing important properties for therapeutics. This is a general approach using straightforward chemistry that can be tailored for various applications by numerous laboratories.
线粒体在维持细胞代谢稳态、细胞存活和细胞死亡方面发挥着核心作用,并产生细胞的大部分能量。线粒体通过动态(分裂和融合)和质量控制机制来维持其稳态,包括自噬,即主要由 Pink1/Parkin 途径介导的受损线粒体的清除。Pink1 是一种丝氨酸/苏氨酸激酶,它调节线粒体功能,迄今为止,许多分子机制仍然未知 Pink1 在线粒体稳态和细胞命运中的活性。肽是重要的生物介质,具有显著的效力、选择性和低毒性,但它们有两个主要限制,即口服生物利用度低和稳定性差。在此,我们合理设计了一种靶向 Pink1 的线性肽,并使用简单的化学方法,开发了具有类药性的分子探针,以进一步表征 Pink1。最初,我们将一个穿透细胞的肽和一个连接子连接起来,以绘制 Pink1 的 3D 结构及其相互作用位点。接下来,我们将一个荧光染料与肽连接起来,用于细胞成像。最后,我们开发了具有提高稳定性和结合亲和力的环状肽。总的来说,我们提出了一种将非渗透性线性肽转化为具有治疗重要特性的研究工具的简便方法。这是一种使用简单化学的通用方法,可以通过许多实验室针对各种应用进行定制。