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纳米颗粒-蛋白质相互作用:治疗方法和超分子化学。

Nanoparticle-Protein Interactions: Therapeutic Approaches and Supramolecular Chemistry.

机构信息

Inorganic Chemistry and Center for Nanointegration Duisburg-Essen (CeNIDE), University of Duisburg-Essen , Universitaetsstr. 5-7, 45117 Essen, Germany.

出版信息

Acc Chem Res. 2017 Jun 20;50(6):1383-1390. doi: 10.1021/acs.accounts.7b00051. Epub 2017 May 8.

DOI:10.1021/acs.accounts.7b00051
PMID:28480714
Abstract

Research on nanoparticles has evolved into a major topic in chemistry. Concerning biomedical research, nanoparticles have decisively entered the field, creating the area of nanomedicine where nanoparticles are used for drug delivery, imaging, and tumor targeting. Besides these functions, scientists have addressed the specific ways in which nanoparticles interact with biomolecules, with proteins being the most prominent example. Depending on their size, shape, charge, and surface functionality, specifically designed nanoparticles can interact with proteins in a defined way. Proteins have typical dimensions of 5-20 nm. Ultrasmall nanoparticles (size about 1-2 nm) can address specific epitopes on the surface of a protein, for example, an active center of an enzyme. Medium-sized nanoparticles (size about 5 nm) can interact with proteins on a 1:1 basis. Large nanoparticles (above 20 nm) are big in comparison to many proteins and therefore are at the borderline to a two-dimensional surface onto which a protein will adsorb. This can still lead to irreversible structural changes in a protein and a subsequent loss of function. However, as most cells readily take up nanoparticles of almost any size, it is easily possible to use nanoparticles as transporters for proteins into a cell, for example, to address an internal receptor. Much work has been dedicated to this approach, but it is constrained by two processes that can only be observed in living cells or organisms. First, nanoparticles are usually taken up by endocytosis and are delivered into an intracellular endosome. After fusion with a lysosome, a degradation or denaturation of the protein cargo by the acidic environment or by proteases may occur before it can enter the cytoplasm. Second, nanoparticles are rapidly coated with proteins upon contact with biological media like blood. This so-called protein corona influences the contact with other proteins, cells, or tissue and may prevent the desired interaction. Essentially, these effects cannot be understood in purely chemical approaches but require biological environments and systems because the underlying processes are simply too complicated to be modeled in nonbiological systems. The area of nanoparticle-protein interactions strongly relies on different approaches: Synthetic chemistry is involved to prepare, stabilize, and functionalize nanoparticles. High-end analytical chemistry is required to understand the nature of a nanoparticle surface and the steps of its interaction with proteins. Concepts from supramolecular chemistry help to understand the complex noncovalent interactions between the surfaces of proteins and nanoparticles. Protein chemistry and biophysical chemistry are required to understand the behavior of a protein in contact with a nanoparticle. Finally, all chemical concepts must live up to the "biological reality", first in cell culture experiments in vitro and finally in animal or human experiments in vivo, to open new therapies in the 21st century. This interdisciplinary approach makes the field highly exciting but also highly demanding for chemists who, however, have to learn to understand the language of other areas.

摘要

纳米粒子的研究已经发展成为化学领域的一个主要课题。在生物医学研究中,纳米粒子已经果断地进入了这个领域,创造了纳米医学领域,在这个领域中,纳米粒子被用于药物输送、成像和肿瘤靶向。除了这些功能外,科学家们还研究了纳米粒子与生物分子相互作用的特定方式,其中蛋白质是最突出的例子。根据其大小、形状、电荷和表面功能,专门设计的纳米粒子可以以特定的方式与蛋白质相互作用。蛋白质的典型尺寸为 5-20nm。超小纳米粒子(尺寸约为 1-2nm)可以与蛋白质表面的特定表位相互作用,例如酶的活性中心。中等大小的纳米粒子(尺寸约为 5nm)可以与蛋白质以 1:1 的比例相互作用。大的纳米粒子(大于 20nm)与许多蛋白质相比体积较大,因此处于蛋白质将吸附的二维表面的边界。这仍然会导致蛋白质结构的不可逆变化,并导致其功能丧失。然而,由于大多数细胞很容易吸收几乎任何大小的纳米粒子,因此很容易将纳米粒子用作蛋白质进入细胞的载体,例如,用于靶向内部受体。已经做了很多工作来研究这种方法,但它受到两个只能在活细胞或生物体中观察到的过程的限制。首先,纳米粒子通常通过内吞作用被吸收,并被递送到细胞内的内体中。在与溶酶体融合后,蛋白质货物可能会在进入细胞质之前被酸性环境或蛋白酶降解或变性。其次,纳米粒子与血液等生物介质接触时会迅速被蛋白质包裹。这种所谓的蛋白质冠影响与其他蛋白质、细胞或组织的接触,可能会阻止所需的相互作用。从本质上讲,这些效应不能仅通过纯化学方法来理解,而需要生物环境和系统,因为底层过程过于复杂,无法在非生物系统中进行建模。纳米粒子-蛋白质相互作用领域强烈依赖于不同的方法:合成化学用于制备、稳定和功能化纳米粒子。需要高端分析化学来了解纳米粒子表面的性质及其与蛋白质相互作用的步骤。超分子化学的概念有助于理解蛋白质和纳米粒子表面之间复杂的非共价相互作用。蛋白质化学和生物物理化学用于理解蛋白质与纳米粒子接触时的行为。最后,所有化学概念都必须符合“生物现实”,首先是在体外细胞培养实验中,最后是在动物或人体实验中,以在 21 世纪开辟新的治疗方法。这种跨学科的方法使该领域非常令人兴奋,但也对化学家提出了很高的要求,然而,化学家必须学会理解其他领域的语言。

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