Cytopathic mechanisms of HIV-I

被引:42
作者
Costin, Joshua M. [1 ]
机构
[1] Florida Gulf Coast Univ, Dept Biol, Biotechnol Res Grp, Ft Myers, FL 33965 USA
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; ION-CHANNEL ACTIVITY; COXSACKIEVIRUS 2B PROTEIN; SEMLIKI-FOREST-VIRUS; HEPATITIS-C-VIRUS; PNEUMOCYSTIS-CARINII-PNEUMONIA; MULTINUCLEATED GIANT-CELLS; LENTIVIRUS LYTIC PEPTIDES; AMINO-ACID SUBSTITUTIONS; ENVELOPE GLYCOPROTEIN;
D O I
10.1186/1743-422X-4-100
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The human immunodeficiency virus type 1 (HIV-I) has been intensely investigated since its discovery in 1983 as the cause of acquired immune deficiency syndrome (AIDS). With relatively few proteins made by the virus, it is able to accomplish many tasks, with each protein serving multiple functions. The Envelope glycoprotein, composed of the two noncovalently linked subunits, SU (surface glycoprotein) and TM (transmembrane glycoprotein) is largely responsible for host cell recognition and entry respectively. While the roles of the N-terminal residues of TM is well established as a fusion pore and anchor for Env into cell membranes, the role of the C-terminus of the protein is not well understood and is fiercely debated. This review gathers
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