50-nm Gas-filled Protein Nanostructures to Enable the Access of Lymphatic Cells by Ultrasound Technologies.
Qionghua ShenZongru LiYixian WangMatthew D MeyerMarc T De GuzmanJanie C LimHan XiaoRichard R BouchardGeorge J LuPublished in: Advanced materials (Deerfield Beach, Fla.) (2024)
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 50nm 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. 50nm GVs can be produced in bacteria, purified through centrifugation, and remain stable for months. Interstitially injected 50nm 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 50nm 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. This article is protected by copyright. All rights reserved.
Keyphrases
- photodynamic therapy
- lymph node
- induced apoptosis
- cell cycle arrest
- gold nanoparticles
- drug delivery
- magnetic resonance imaging
- gene expression
- room temperature
- healthcare
- endoplasmic reticulum stress
- light emitting
- carbon dioxide
- cell death
- deep learning
- squamous cell carcinoma
- case report
- small molecule
- cell proliferation
- computed tomography
- protein protein
- pi k akt
- rectal cancer