A novel modified peptide derived from membrane-proximal external region of human immunodeficiency virus type 1 envelope significantly enhances retrovirus infection

作者：Zhang Lishuang; Jiang Chunlai; Zhang Huayan; Gong Xin; Yang Lan; Miao Liang; Shi Yuhua; Zhang Yan; Kong Wei; Zhang Chuntao; Shan Yaming^*

来源：Journal of Peptide Science, 2014, 20(1): 46-54.

DOI：10.1002/psc.2587

• MPER-based peptides
• HIV-1 infection enhancement
• aromatic
• cationic
• retroviral transduction

Efficient gene transfer is a critical goal in retroviral transduction. Several peptides capable of forming amyloid fibrils, such as the 39-residue semen-derived infection-enhancing peptide (SEVI), have demonstrated the ability to boost retroviral gene delivery. Here, a 13-residue peptide P13 (Ac-(NWFDITNWLWYIK683)-N-671) derived from the membrane-proximal external region of the human immunodeficiency virus type 1 (HIV-1) gp41 transmembrane protein, together with its 16-residue peptide derivative (P16) were found to enhance HIV-1 infection significantly. Both peptides, P13 and P16, could form amyloid fibril structures to potently enhance HIV-1 infectivity. Further investigations showed that both aromatic Trp residues and cationic Lys residues contributed to the enhancement of HIV-1 infection by these two active peptides. P16 could more effectively augment HIV-1 YU-2 infection than SEVI, implying its potential applications as a tool in the lab to improve gene transfer rates.

• 出版日期2014-1
• 单位吉林大学