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基于选定金属配合物和金属纳米粒子的细胞内催化:向催化金属药物发展的进展。

Intracellular Catalysis with Selected Metal Complexes and Metallic Nanoparticles: Advances toward the Development of Catalytic Metallodrugs.

机构信息

Inorganic Chemistry I-Bioinorganic Chemistry , Ruhr University Bochum , Universitätsstrasse 150 , 44780-D Bochum , Germany.

出版信息

Chem Rev. 2019 Jan 23;119(2):829-869. doi: 10.1021/acs.chemrev.8b00493. Epub 2019 Jan 8.

Abstract

Platinum-containing drugs (e.g., cisplatin) are among the most frequently used chemotherapeutic agents. Their tremendous success has spurred research and development of other metal-based drugs, with notable achievements. Generally, the vast majority of metal-based drug candidates in clinical and developmental stages are stoichiometric agents, i.e., each metal complex reacts only once with their biological target. Additionally, many of these metal complexes are involved in side reactions, which not only reduce the effective amount of the drug but may also cause toxicity. On a separate note, transition metal complexes and nanoparticles have a well-established history of being potent catalysts for selective molecular transformations, with examples such as the Mo- and Ru-based catalysts for metathesis reactions (Nobel Prize in 2005) or palladium catalysts for C-C bond forming reactions such as Heck, Negishi, or Suzuki reactions (Nobel Prize in 2010). Also, notably, no direct biological equivalent of these transformations exists in a biological environment such as bacteria or mammalian cells. It is, therefore, only logical that recent interest has focused on developing transition-metal based catalytic systems that are capable of performing transformations inside cells, with the aim of inducing medicinally relevant cellular changes. Because unlike in stoichiometric reactions, a catalytically active compound may turn over many substrate molecules, only very small amounts of such a catalytic metallodrug are required to achieve a desired pharmacologic effect, and therefore, toxicity and side reactions are reduced. Furthermore, performing catalytic reactions in biological systems also opens the door for new methodologies to study the behavior of biomolecules in their natural state, e.g., via in situ labeling or by increasing/depleting their concentration at will. There is, of course, an art to the choice of catalysts and reactions which have to be compatible with biological conditions, namely an aqueous, oxygen-containing environment. In this review, we aim to describe new developments that bring together the far-distant worlds of transition-metal based catalysis and metal-based drugs, in what is termed "catalytic metallodrugs". Here we will focus on transformations that have been performed on small biomolecules (such as shifting equilibria like in the NAD/NADH or GSH/GSSG couples), on non-natural molecules such as dyes for imaging purposes, or on biomacromolecules such as proteins. Neither reactions involving release (e.g., CO) or transformation of small molecules (e.g., O production), degradation of biomolecules such as proteins, RNA or DNA nor light-induced medicinal chemistry (e.g., photodynamic therapy) are covered, even if metal complexes are centrally involved in those. In each section, we describe the (inorganic) chemistry involved, as well as selected examples of biological applications in the hope that this snapshot of a new but quickly developing field will indeed inspire novel research and unprecedented interactions across disciplinary boundaries.

摘要

含铂药物(例如顺铂)是最常使用的化疗药物之一。它们的巨大成功推动了其他基于金属的药物的研究和开发,并取得了显著的成果。通常,临床和开发阶段的绝大多数基于金属的候选药物都是化学计量型药物,即每个金属配合物仅与它们的生物靶标发生一次反应。此外,许多这些金属配合物参与副反应,这不仅降低了药物的有效量,还可能导致毒性。另外,过渡金属配合物和纳米颗粒作为选择性分子转化的有力催化剂已有良好的历史记载,例如用于复分解反应的 Mo 和 Ru 基催化剂(2005 年诺贝尔化学奖)或用于 C-C 键形成反应的钯催化剂,如 Heck、Negishi 或 Suzuki 反应(2010 年诺贝尔化学奖)。此外,值得注意的是,在细菌或哺乳动物细胞等生物环境中,不存在这些转化的直接生物学等同物。因此,最近的兴趣集中在开发能够在细胞内进行转化的基于过渡金属的催化系统上,目的是诱导具有医学相关性的细胞变化。因为与化学计量反应不同,催化活性化合物可能使许多底物分子转化,因此只需要非常少量的这种催化金属药物就可以达到所需的药理效果,从而降低毒性和副反应。此外,在生物系统中进行催化反应也为研究生物分子在其自然状态下的行为开辟了新的方法,例如通过原位标记或随意增加/减少它们的浓度。当然,选择与生物条件兼容的催化剂和反应需要一定的技巧,即含有水和氧气的环境。在这篇综述中,我们旨在描述将过渡金属催化和基于金属的药物这两个截然不同的世界结合在一起的新发展,即“催化金属药物”。在这里,我们将重点介绍已经在小分子(如 NAD/NADH 或 GSH/GSSG 偶联物中的平衡转移)、非天然分子(如用于成像的染料)或生物大分子(如蛋白质)上进行的转化。既不涉及小分子的释放(例如 CO)或转化(例如 O 生成)、生物分子(如蛋白质、RNA 或 DNA)的降解,也不涉及光诱导的药物化学(例如光动力疗法)的反应均不在此范围内,即使金属配合物在其中也起到了核心作用。在每个部分中,我们都描述了所涉及的(无机)化学,以及生物应用的一些示例,希望这一新但发展迅速的领域的快照确实能够激发新的研究,并在跨学科边界进行前所未有的互动。

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