4.4 Article

Crystallization and preliminary X-ray diffraction analysis of human adenovirus

期刊

VIROLOGY
卷 402, 期 1, 页码 209-214

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.virol.2010.03.028

关键词

Human adenovirus; Virus structure; Capsid structure; Crystallization; Structure determination

类别

资金

  1. National Cancer Institute [Y1-CO-1020]
  2. National Institute of General Medical Science [Y1-GM-1104]
  3. U.S. Department of Energy, Basic Energy Sciences, Office of Science [DE-AC02-06CH11357]
  4. NIH [R01 AI070771, EY011431, HL54352]

向作者/读者索取更多资源

Replication-defective and conditionally replicating adenovirus (AdV) vectors are currently being utilized in similar to 25% of human gene transfer clinical trials. Unfortunately, progress in vector development has been hindered by a lack of accurate structural information. Here we describe the crystallization and preliminary X-ray diffraction analysis of a HAdV5 vector that displays a short flexible fiber derived from HAdV35. Crystals of Ad35F were grown in 100 mM HEPES pH 7.0, 200 mM Ca(OAc)(2), 14% PEG 550 MME, 15% glycerol in 100 mM Tris-HCI 8.5. Freshly grown crystals diffracted well to 4.5 angstrom resolution and weakly to 3.5 angstrom at synchrotron sources. HAdV crystals belong to space group P1 with unit cell parameters a = 854.03 angstrom, b = 855.17 angstrom, c = 865.24 angstrom, alpha= 119.57 degrees. beta= 91.71 degrees, gamma= 118.08 degrees with a single particle in the unit cell. Self-rotation and locked-rotation function analysis allowed the determination of the particle orientation. Molecular replacement, density modification and phase-extension procedures are being employed for structure determination. (C) 2010 Elsevier Inc. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据