Bhattacharya Sonia, Jenkins Matthew C, Keshavarz-Joud Parisa, Bourque Alisyn Retos, White Keiyana, Alvarez Barkane Amina M, Bryksin Anton V, Hernandez Carolina, Kopylov Mykhailo, Finn M G
School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, GA 30332, USA.
Parker H. Petit Institute for Bioengineering and Biosciences, Georgia Institute of Technology, Atlanta, GA, 30332, USA.
bioRxiv. 2024 Feb 26:2024.02.24.581861. doi: 10.1101/2024.02.24.581861.
Protein nanoparticles are effective platforms for antigen presentation and targeting effector immune cells in vaccine development. Encapsulins are a class of protein-based microbial nanocompartments that self-assemble into icosahedral structures with external diameters ranging from 24 to 42 nm. Encapsulins from were designed to package bacterial RNA when produced in and were shown to have immunogenic and self-adjuvanting properties enhanced by this RNA. We genetically incorporated a 20-mer peptide derived from a mutant strain of the SARS-CoV-2 receptor binding domain (RBD) into the encapsulin protomeric coat protein for presentation on the exterior surface of the particle. This immunogen elicited conformationally-relevant humoral responses to the SARS-CoV-2 RBD. Immunological recognition was enhanced when the same peptide was presented in a heterologous prime/boost vaccination strategy using the engineered encapsulin and a previously reported variant of the PP7 virus-like particle, leading to the development of a selective antibody response against a SARS-CoV-2 RBD point mutant. While generating epitope-focused antibody responses is an interplay between inherent vaccine properties and B/T cells, here we demonstrate the use of orthogonal nanoparticles to fine-tune the control of epitope focusing.
蛋白质纳米颗粒是疫苗开发中用于抗原呈递和靶向效应免疫细胞的有效平台。封装蛋白是一类基于蛋白质的微生物纳米隔室,可自组装成外径为24至42纳米的二十面体结构。来自[具体来源]的封装蛋白在[具体宿主]中产生时被设计用于包裹细菌RNA,并显示出被这种RNA增强的免疫原性和自佐剂特性。我们将源自严重急性呼吸综合征冠状病毒2(SARS-CoV-2)受体结合域(RBD)突变株的20聚体肽基因整合到封装蛋白原聚体外壳蛋白中,以便在颗粒外表面呈递。这种免疫原引发了针对SARS-CoV-2 RBD的构象相关体液反应。当使用工程化封装蛋白和先前报道的PP7病毒样颗粒变体以异源初免/加强疫苗接种策略呈递相同肽时,免疫识别得到增强,从而产生针对SARS-CoV-2 RBD点突变体的选择性抗体反应。虽然产生聚焦表位的抗体反应是固有疫苗特性与B/T细胞之间的相互作用,但在这里我们展示了使用正交纳米颗粒来微调对表位聚焦的控制。