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利用场发射扫描电子显微镜评估重组腺病毒的稳定性。

The use of field emission scanning electron microscopy to assess recombinant adenovirus stability.

作者信息

Obenauer-Kutner Linda J, Ihnat Peter M, Yang Tong-Yuan, Dovey-Hartman Barbara J, Balu Arthi, Cullen Constance, Bordens Ronald W, Grace Michael J

机构信息

Biotechnology Development, Schering-Plough Research Institute, Union, NJ 07083, USA.

出版信息

Hum Gene Ther. 2002 Sep 20;13(14):1687-96. doi: 10.1089/104303402760293538.

Abstract

A field emission scanning electron microscopy (FESEM) method was developed to assess the stability of a recombinant adenovirus (rAd). This method was designed to simultaneously sort, count, and size the total number of rAd viral species observed within an image field. To test the method, a preparation of p53 transgene-expressing recombinant adenovirus (rAd/p53) was incubated at 37 degrees C and the viral particles were evaluated by number, structure, and degree of aggregation as a function of time. Transmission electron microscopy (TEM) was also used to obtain ultrastructural detail. In addition, the infectious activity of the incubated rAd/p53 samples was determined using flow cytometry. FESEM image-analysis revealed that incubation at 37 degrees C resulted in a time-dependent decrease in the total number of detectable single rAd/p53 virus particles and an increase in apparent aggregates composed of more than three adenovirus particles. There was also an observed decrease in both the diameter and perimeter of the single rAd/p53 viral particles. TEM further revealed the accumulation of damaged single particles with time at 37 degrees C. The results of this study demonstrate that FESEM, coupled with sophisticated image analysis, may be an important tool in quantifying the distribution of aggregated species and assessing the overall stability of rAd samples.

摘要

开发了一种场发射扫描电子显微镜(FESEM)方法来评估重组腺病毒(rAd)的稳定性。该方法旨在同时对图像视野内观察到的rAd病毒种类总数进行分类、计数和测量大小。为了测试该方法,将表达p53转基因的重组腺病毒(rAd/p53)制剂在37℃下孵育,并根据时间对病毒颗粒的数量、结构和聚集程度进行评估。还使用透射电子显微镜(TEM)来获得超微结构细节。此外,使用流式细胞术测定孵育后的rAd/p53样品的感染活性。FESEM图像分析显示,在37℃下孵育导致可检测到的单个rAd/p53病毒颗粒总数随时间减少,且由三个以上腺病毒颗粒组成的明显聚集体增加。还观察到单个rAd/p53病毒颗粒的直径和周长均减小。TEM进一步显示,在37℃下,受损单个颗粒随时间积累。本研究结果表明,FESEM结合复杂的图像分析,可能是量化聚集物种分布和评估rAd样品整体稳定性的重要工具。

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