Institute of Environmental, Chemical, and Pharmaceutical Sciences, Federal University of São Paulo, Rua São Nicolau, 210, 09972-270 Diadema, Brazil.
Departmento de Bioquimica, Escola Paulista de Medicina, Universidade Federal, Rua Pedro de Toledo, 669, 04039-032 São Paulo, Brazil.
Biochim Biophys Acta Biomembr. 2019 Oct 1;1861(10):182992. doi: 10.1016/j.bbamem.2019.05.014. Epub 2019 May 23.
Trastuzumab (Tmab) is a monoclonal antibody administered as targeted therapy for HER2-positive breast cancer whose molecular interactions at the HER2 receptor microenvironment are not completely clarified yet. This paper describes the influence of Tmab in the molecular organization of films of biological-relevant molecules at the air water interface. For that, we spread components of tumorigenic and non-tumorigenic cells directly on the air-water interface. The physicochemical properties of the films were investigated with surface pressure-area isotherms and Brewster angle microscopy, and distinction between the cellular lines with higher or lower amount of HER2 could be detected based on the physicochemical properties of the interfacial films. The systems organized at the air-water interface were transferred to solid supports as Langmuir-Blodgett films and the nano-scale morphology investigated with atomic force microscopy. The overall results related to Tmab interacting with the films lead to the conclusion that Tmab tends to condense rich-HER2 films, causing irregular dimerization of the receptor protein, changing the membrane topography of the films, with formation of phases with different levels of reflectivity and aggregation morphology, and finally revealing that the interaction of the antibody with proteo-lipidic biointerfaces is modulated by the film composition. We believe that novel perspectives concerning the molecular interactions in the plasma membrane microenvironment through Langmuir monolayers can be obtained from this work in order to enhance the Tmab-based cancer therapy.
曲妥珠单抗(Tmab)是一种单克隆抗体,作为针对 HER2 阳性乳腺癌的靶向治疗药物,其在 HER2 受体微环境中的分子相互作用尚未完全阐明。本文描述了 Tmab 对生物相关分子在气液界面薄膜中分子组织的影响。为此,我们将肿瘤细胞和非肿瘤细胞的成分直接铺展在气液界面上。通过表面压-面积等温线和布鲁斯特角显微镜研究了薄膜的物理化学性质,并基于界面薄膜的物理化学性质可以区分具有较高或较低 HER2 量的细胞系。在气液界面上组织的系统被转移到固体载体上作为 Langmuir-Blodgett 薄膜,并通过原子力显微镜研究了纳米级形貌。与 Tmab 相互作用的薄膜的整体结果表明,Tmab 倾向于浓缩富含 HER2 的薄膜,导致受体蛋白的不规则二聚化,改变薄膜的膜形貌,形成具有不同反射率水平和聚集形态的相,最终表明抗体与蛋白脂生物界面的相互作用受薄膜组成的调节。我们相信,通过 Langmuir 单层可以获得关于质膜微环境中分子相互作用的新视角,以增强基于 Tmab 的癌症治疗。