Golbek Thaddeus W, Okur Halil I, Kulik Sergey, Dedic Jan, Roke Sylvie, Weidner Tobias
Department of Chemistry, Aarhus University, 8000 Aarhus C, Denmark.
Laboratory for Fundamental BioPhotonics (LBP), Institute of Bio-engineering (IBI), School of Engineering (STI), École Polytechnique Fédérale de Lausanne (EPFL), CH-1015 Lausanne, Switzerland.
Langmuir. 2023 May 9;39(18):6447-6454. doi: 10.1021/acs.langmuir.3c00276. Epub 2023 Apr 26.
When a nanoparticle (NP) is introduced into a biological environment, its identity and interactions are immediately attributed to the dense layer of proteins that quickly covers the particle. The formation of this layer, dubbed the protein corona, is in general a combination of proteins interacting with the surface of the NP and a contest between other proteins for binding sites either at the surface of the NP or upon the dense layer. Despite the importance for surface engineering and drug development, the molecular mechanisms and structure behind interfacial biomolecule action have largely remained elusive. We use ultrafast sum frequency scattering (SFS) spectroscopy to determine the structure and the mode of action by which these biomolecules interact with and manipulate interfaces. The majority of work in the field of sum frequency generation has been done on flat model interfaces. This limits some important membrane properties such as membrane fluidity and dimensionality─important factors in biomolecule-membrane interactions. To move toward three-dimensional (3D) nanoscopic interfaces, we utilize SFS spectroscopy to interrogate the surface of 3D lipid monolayers, which can be used as a model lipid-based nanocarrier system. In this study, we have utilized SFS spectroscopy to follow the action of lysozyme. SFS spectra in the amide I region suggest that there is lysozyme at the interface and that the lysozyme induces an increased lipid monolayer order. The binding of lysozyme with the NP is demonstrated by an increase in acyl chain order determined by the ratio of the CH symmetric and CH symmetric peak amplitudes. Furthermore, the lipid headgroup orientation s-PO change strongly supports lysozyme insertion into the lipid layer causing lipid disruption and reorientation. Altogether, with SFS, we have made a huge stride toward understanding the binding and structure change of proteins within the protein corona.
当纳米颗粒(NP)被引入生物环境中时,其特性和相互作用会立即归因于迅速覆盖在颗粒表面的致密蛋白质层。这层被称为蛋白质冠的形成,通常是蛋白质与NP表面相互作用以及其他蛋白质在NP表面或致密层上争夺结合位点的综合结果。尽管对表面工程和药物开发很重要,但界面生物分子作用背后的分子机制和结构在很大程度上仍然难以捉摸。我们使用超快和频散射(SFS)光谱来确定这些生物分子与界面相互作用并操纵界面的结构和作用方式。和频产生领域的大部分工作是在平面模型界面上进行的。这限制了一些重要的膜特性,如膜流动性和维度——生物分子与膜相互作用中的重要因素。为了转向三维(3D)纳米界面,我们利用SFS光谱来研究3D脂质单层的表面,其可作为基于脂质的纳米载体系统模型。在本研究中,我们利用SFS光谱来追踪溶菌酶的作用。酰胺I区域的SFS光谱表明界面处存在溶菌酶,并且溶菌酶会诱导脂质单层有序性增加。通过由CH对称峰和CH对称峰振幅之比确定的酰基链有序性增加,证明了溶菌酶与NP的结合。此外,脂质头基取向s-PO的强烈变化有力地支持了溶菌酶插入脂质层导致脂质破坏和重新取向。总之,通过SFS,我们在理解蛋白质冠内蛋白质的结合和结构变化方面取得了巨大进展。