CHARACTERIZATION OF A PUTATIVE CELLULAR RECEPTOR FOR HIV-1 TRANSMEMBRANE GLYCOPROTEIN USING SYNTHETIC PEPTIDES

被引:74
作者
QURESHI, NM
COY, DH
GARRY, RF
HENDERSON, LA
机构
[1] TULANE UNIV, SCH MED, DEPT PATHOL, 1430 TULANE AVE, NEW ORLEANS, LA 70112 USA
[2] TULANE UNIV, SCH MED, DEPT MICROBIOL & IMMUNOL, NEW ORLEANS, LA 70112 USA
[3] TULANE UNIV, SCH MED, DEPT MED, NEW ORLEANS, LA 70112 USA
关键词
Cytopathology; HIV-1; Receptor; Therapy; Transmembrane glycoprotein;
D O I
10.1097/00002030-199006000-00009
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 transmembrane glycoprotein (gp41 or TM) of HIV-1 contains limited sequence similarity to TM of some immunosuppressive animal retroviruses. A specific HIV-1 TM sequence, denoted CS3, inhibits T-cell activation in vitro and antibody specific to CS3 has been linked to the absence of disease. CS3, when conjugated to human serum albumin (HSA) and labeled with fluorescein, binds specifically to CD4+ cell lines. Cross-linking of CS3-HSA to its binding activity on the CD4+ cell line RH9 reveals a putative subunit size of approximately 44 kD. Incubation of RH9 cells with CS3-HSA prior to addition of HIV-1 prevented HIV-1-mediated cell lysis and inhibited infection. These results suggest that the CS3 region of TM plays an important role in the pathogenesis of the AIDS virus, HIV-1.
引用
收藏
页码:553 / 558
页数:6
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