Document 3288 DOCN M94A3288 TI HIV-1 gp160 processing in furin-defective LoVo cells. DT 9412 AU Nagai Y; Ohnishi Y; Shioda T; Institute of Medical Science, University of Tokyo, Japan. SO Int Conf AIDS. 1994 Aug 7-12;10(1):110 (abstract no. PA0057). Unique Identifier : AIDSLINE ICA10/94369287 AB Furin, a subtilisin-like mammalian endopprotease, is believed to be responsible for processing various proprotein precursors of cellular and viral origin including the gp160 of HIV-1, which share the consensus processing site motif, Arg-X-Lys/Arg-Arg, for protease recognition. To confirm and extend the concept that the gp160 is processed by furin, we used here a cell line, LoVo, which was recently demonstrated to be furin-defective. Unexpectedly, LoVo cells were found to process gp160 as efficiently as normal cell lines do, hence being able to fuse with CD4-expressing HeLa cells and to produce fully infectious virions. On the other hand, the same cell line was almost totally incapable of processing Newcastle disease virus (NDV) fusion glycoprotein with a similar oligobasic cleavage-recognition motif, providing a strong case of furin-mediated processing. Our present study thus raises a further need to search and identify the proteinases involved in HIV-1 gp160 processing rather than supports the notion that furin is responsible. DE Amino Acid Sequence Binding Sites Cell Fusion Cell Line Consensus Sequence Gene Products, env/GENETICS/*METABOLISM Hela Cells Human HIV-1/*METABOLISM Molecular Sequence Data Newcastle Disease Virus/METABOLISM Protein Precursors/GENETICS/*METABOLISM Protein Processing, Post-Translational Substrate Specificity Subtilisins/*METABOLISM Viral Fusion Proteins/METABOLISM MEETING ABSTRACT SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).