Construction and characterization of soluble, cleaved, and stabilized trimeric Env proteins based on HIV type 1 Env subtype A

被引:20
作者
Beddows, Simon
Kirschner, Marc
Campbell-Gardener, Lila
Franti, Michael
Dey, Antu K.
Iyer, Sai Prasad N.
Maddon, Paul J.
Paluch, Maciej
Master, Aditi
Overbaugh, Julie
VanCott, Thomas
Olson, William C.
Moore, John P.
机构
[1] Cornell Univ, Weill Med Coll, Dept Immunol & Microbiol, New York, NY 10021 USA
[2] Progen Pharmaceut Inc, Tarrytown, NY 10591 USA
[3] Fred Hutchinson Canc Res Ctr, Div Human Biol, Seattle, WA 98109 USA
[4] Henry M Jackson Fdn, Rockville, MD 20850 USA
关键词
D O I
10.1089/aid.2006.22.569
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The generation of an antibody response capable of neutralizing a broad range of clinical isolates remains an important goal of human immunodeficiency virus type 1 (HIV-1) vaccine development. Envelope glycoprotein (Env)-based vaccine candidates will also need to take into account the extensive genetic diversity of circulating HIV-1 strains. We describe here the generation of soluble, stabilized, proteolytically cleaved, trimeric forms of Env (SOSIP gp140 proteins) based on contemporary Env subtype A viruses from East Africa. We discuss issues associated with the construction, purification, and characterization of such complex proteins; not all env sequences allow the expression of trimeric proteins. However, stabilized trimers from one such protein, KNH1144 SOSIP gp140, were successfully made. These proteins are now being prepared for preclinical immunogenicity studies.
引用
收藏
页码:569 / 579
页数:11
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