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气体囊泡与血液的相互作用增强超声成像对比度。

Gas vesicle-blood interactions enhance ultrasound imaging contrast.

作者信息

Ling Bill, Ko Jeong Hoon, Stordy Benjamin, Zhang Yuwei, Didden Tighe F, Malounda Dina, Swift Margaret B, Chan Warren C W, Shapiro Mikhail G

机构信息

Division of Chemistry and Chemical Engineering, California Institute of Technology; Pasadena, CA 91125, USA.

These authors contributed equally to this work.

出版信息

bioRxiv. 2023 Jul 25:2023.07.24.550434. doi: 10.1101/2023.07.24.550434.

Abstract

Gas vesicles (GVs) are genetically encoded, air-filled protein nanostructures of broad interest for biomedical research and clinical applications, acting as imaging and therapeutic agents for ultrasound, magnetic resonance, and optical techniques. However, the biomedical applications of GVs as a systemically injectable nanomaterial have been hindered by a lack of understanding of GVs' interactions with blood components, which can significantly impact performance. Here, we investigate the dynamics of GVs in the bloodstream using a combination of ultrasound and optical imaging, surface functionalization, flow cytometry, and mass spectrometry. We find that erythrocytes and serum proteins bind to GVs and shape their acoustic response, circulation time, and immunogenicity. We show that by modifying the GV surface, we can alter these interactions and thereby modify GVs' performance. These results provide critical insights for the development of GVs as agents for nanomedicine.

摘要

气体囊泡(GVs)是具有遗传编码的、充满空气的蛋白质纳米结构,在生物医学研究和临床应用中备受关注,可作为超声、磁共振和光学技术的成像及治疗剂。然而,由于对GVs与血液成分的相互作用缺乏了解,这可能会显著影响其性能,从而阻碍了GVs作为可全身注射纳米材料的生物医学应用。在此,我们结合超声和光学成像、表面功能化、流式细胞术和质谱技术,研究了GVs在血液中的动力学。我们发现红细胞和血清蛋白会与GVs结合,并塑造其声学响应、循环时间和免疫原性。我们表明,通过修饰GV表面,我们可以改变这些相互作用,从而改变GVs的性能。这些结果为将GVs开发为纳米医学制剂提供了关键见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0474/10402017/71e1591e3b5c/nihpp-2023.07.24.550434v1-f0001.jpg

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