Enhancement of Human Immunodeficiency Virus Type 1 (HIV-1) Infection via Increased Membrane Fluidity by a Cationic Polymer

Author:

Owada Takashi12,Miyashita Yuko2,Motomura Tadahiro2,Onishi Makoto2,Yamashita Shuzo2,Yamamoto Naoki1

Affiliation:

1. Department of Microbiology; Tokyo Medical and Dental University School of Medicine; Bunkyo-ku Tokyo 113-0034 Japan

2. Department of New Materials Section; Terumo Research and Development Center; Kanagawa 259-0151 Japan

Publisher

Wiley

Subject

Virology,Immunology,Microbiology

Reference56 articles.

1. Analysis of the secondary structure of the human immunodeficiency virus (HIV) proteins p17, gp120 and gp41 by computer modeling based on neural network methods;Andreassen;J. Acquir. Immune Defic. Syndr.,1990

2. Internalization of the human immunodeficiency virus does not require the cytoplasmic domain of CD4;Bedinger;Nature,1988

3. Target cell-specific determinants of membrane fusion within the human immunodeficiency virus type 1 gp120 third variable region and gp41 aminoterminus;Bergeron;J. Virol.,1992

4. The galactosyl ceramide/sulfatide receptor binding region of HIV-1 gp120 maps to amino acids 206-275;Bhat;AIDS Res. Hum. Retroviruses,1993

5. Mode of insertion into a lipid membrane of the N-terminal HIV gp41 peptide segment;Brasseur;AIDS Res. Hum. Retroviruses,1988

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