Shen Qionghua, Li Zongru, Meyer Matthew D, De Guzman Marc T, Lim Janie C, Bouchard Richard R, Lu George J
bioRxiv. 2023 Jun 28:2023.06.27.546433. doi: 10.1101/2023.06.27.546433.
Ultrasound imaging and ultrasound-mediated gene and drug delivery are rapidly advancing diagnostic and therapeutic methods; however, their use is often limited by the need of microbubbles, which cannot transverse many biological barriers due to their large size. Here we introduce 50-nm gas-filled protein nanostructures derived from genetically engineered gas vesicles that we referred to as GVs. These diamond-shaped nanostructures have hydrodynamic diameters smaller than commercially available 50-nm gold nanoparticles and are, to our knowledge, the smallest stable, free-floating bubbles made to date. GVs can be produced in bacteria, purified through centrifugation, and remain stable for months. Interstitially injected GVs can extravasate into lymphatic tissues and gain access to critical immune cell populations, and electron microscopy images of lymph node tissues reveal their subcellular location in antigen-presenting cells adjacent to lymphocytes. We anticipate that GVs can substantially broaden the range of cells accessible to current ultrasound technologies and may generate applications beyond biomedicine as ultrasmall stable gas-filled nanomaterials.
超声成像以及超声介导的基因和药物递送是快速发展的诊断和治疗方法;然而,它们的应用常常受到微泡需求的限制,微泡由于尺寸较大无法穿过许多生物屏障。在此,我们介绍了源自基因工程气体囊泡的50纳米充气蛋白纳米结构,我们将其称为GVs。这些菱形纳米结构的流体动力学直径小于市售的50纳米金纳米颗粒,据我们所知,是迄今为止制备的最小的稳定、自由漂浮气泡。GVs可在细菌中产生,通过离心纯化,并可稳定保存数月。间质注射的GVs可渗出到淋巴组织中并接触关键免疫细胞群体,淋巴结组织的电子显微镜图像显示它们在与淋巴细胞相邻的抗原呈递细胞中的亚细胞定位。我们预计,GVs可大幅拓宽当前超声技术可触及的细胞范围,并可能作为超小稳定充气纳米材料产生超越生物医学的应用。