The influenza A virus PB1-F2 protein targets the inner mitochondrial membrane via a predicted basic amphipathic helix that disrupts mitochondrial function
被引:175
作者:
Gibbs, JS
论文数: 0引用数: 0
h-index: 0
机构:NIAID, Viral Dis Lab, NIH, Bethesda, MD 20892 USA
Gibbs, JS
Malide, D
论文数: 0引用数: 0
h-index: 0
机构:NIAID, Viral Dis Lab, NIH, Bethesda, MD 20892 USA
Malide, D
Hornung, F
论文数: 0引用数: 0
h-index: 0
机构:NIAID, Viral Dis Lab, NIH, Bethesda, MD 20892 USA
Hornung, F
Bennink, JR
论文数: 0引用数: 0
h-index: 0
机构:NIAID, Viral Dis Lab, NIH, Bethesda, MD 20892 USA
Bennink, JR
Yewdell, JW
论文数: 0引用数: 0
h-index: 0
机构:NIAID, Viral Dis Lab, NIH, Bethesda, MD 20892 USA
Yewdell, JW
机构:
[1] NIAID, Viral Dis Lab, NIH, Bethesda, MD 20892 USA
The 11th influenza A virus gene product is an 87-amino-acid protein provisionally named PB1-F2 (because. it is encoded by an open reading frame overlapping the PB1 open reading frame). A significant fraction of PB1-F2 localizes to the inner mitochondrial membrane in influenza A virus-infected cells. PB1-F2 appears to enhance virus-induced cell death in a cell type-dependent manner. For the present communication we have identified and characterized a region near the COOH terminus of PB1-F2 that is necessary and sufficient for its inner mitochondrial membrane localization, as determined by transient expression of chimeric proteins consisting of elements of PB1-F2 genetically fused to enhanced green fluorescent protein (EGFP) in HeLa cells. Targeting of EGFP to mitochondria by this sequence resulted in the loss of the inner mitochondrial membrane potential, leading to cell death. The mitochondrial targeting sequence (MTS) is predicted to form a positively charged amphipathic et-helix and, as such, is similar to the MTS of the p13(II) protein of human T-cell leukemia virus type 1. We formally demonstrate the functional interchangeability of the two sequences for mitochondrial localization of PB1-F2. Mutation analysis of the putative amphipathic helix in the PB1-F2 reveals that replacement of five basic amino acids with Ala abolishes mitochondrial targeting, whereas mutation of two highly conserved Leu to Ala does not. These findings demonstrate that PB1-F2 possesses an MTS similar to other viral proteins and that this MTS, when fused to EGFP, is capable of independently compromising mitochondrial function and cellular viability.
机构:
Karolinska Inst, Inst Environm Med, Div Mol Toxicol, S-17177 Stockholm, SwedenKarolinska Inst, Inst Environm Med, Div Mol Toxicol, S-17177 Stockholm, Sweden
Neve, EPA
;
Ingelman-Sundberg, M
论文数: 0引用数: 0
h-index: 0
机构:
Karolinska Inst, Inst Environm Med, Div Mol Toxicol, S-17177 Stockholm, SwedenKarolinska Inst, Inst Environm Med, Div Mol Toxicol, S-17177 Stockholm, Sweden
机构:
Penn State Univ, Milton S Hershey Med Ctr, Dept Cellular & Mol Physiol, Coll Med, Hershey, PA 17033 USAPenn State Univ, Milton S Hershey Med Ctr, Dept Cellular & Mol Physiol, Coll Med, Hershey, PA 17033 USA
Scaduto, RC
;
Grotyohann, LW
论文数: 0引用数: 0
h-index: 0
机构:
Penn State Univ, Milton S Hershey Med Ctr, Dept Cellular & Mol Physiol, Coll Med, Hershey, PA 17033 USAPenn State Univ, Milton S Hershey Med Ctr, Dept Cellular & Mol Physiol, Coll Med, Hershey, PA 17033 USA
机构:
La Jolla Inst Allergy & Immunol, Div Cellular Immunol, San Diego, CA 92121 USALa Jolla Inst Allergy & Immunol, Div Cellular Immunol, San Diego, CA 92121 USA
Waterhouse, NJ
;
Ricci, JE
论文数: 0引用数: 0
h-index: 0
机构:
La Jolla Inst Allergy & Immunol, Div Cellular Immunol, San Diego, CA 92121 USALa Jolla Inst Allergy & Immunol, Div Cellular Immunol, San Diego, CA 92121 USA
Ricci, JE
;
Green, DR
论文数: 0引用数: 0
h-index: 0
机构:
La Jolla Inst Allergy & Immunol, Div Cellular Immunol, San Diego, CA 92121 USALa Jolla Inst Allergy & Immunol, Div Cellular Immunol, San Diego, CA 92121 USA
机构:
Karolinska Inst, Inst Environm Med, Div Mol Toxicol, S-17177 Stockholm, SwedenKarolinska Inst, Inst Environm Med, Div Mol Toxicol, S-17177 Stockholm, Sweden
Neve, EPA
;
Ingelman-Sundberg, M
论文数: 0引用数: 0
h-index: 0
机构:
Karolinska Inst, Inst Environm Med, Div Mol Toxicol, S-17177 Stockholm, SwedenKarolinska Inst, Inst Environm Med, Div Mol Toxicol, S-17177 Stockholm, Sweden
机构:
Penn State Univ, Milton S Hershey Med Ctr, Dept Cellular & Mol Physiol, Coll Med, Hershey, PA 17033 USAPenn State Univ, Milton S Hershey Med Ctr, Dept Cellular & Mol Physiol, Coll Med, Hershey, PA 17033 USA
Scaduto, RC
;
Grotyohann, LW
论文数: 0引用数: 0
h-index: 0
机构:
Penn State Univ, Milton S Hershey Med Ctr, Dept Cellular & Mol Physiol, Coll Med, Hershey, PA 17033 USAPenn State Univ, Milton S Hershey Med Ctr, Dept Cellular & Mol Physiol, Coll Med, Hershey, PA 17033 USA
机构:
La Jolla Inst Allergy & Immunol, Div Cellular Immunol, San Diego, CA 92121 USALa Jolla Inst Allergy & Immunol, Div Cellular Immunol, San Diego, CA 92121 USA
Waterhouse, NJ
;
Ricci, JE
论文数: 0引用数: 0
h-index: 0
机构:
La Jolla Inst Allergy & Immunol, Div Cellular Immunol, San Diego, CA 92121 USALa Jolla Inst Allergy & Immunol, Div Cellular Immunol, San Diego, CA 92121 USA
Ricci, JE
;
Green, DR
论文数: 0引用数: 0
h-index: 0
机构:
La Jolla Inst Allergy & Immunol, Div Cellular Immunol, San Diego, CA 92121 USALa Jolla Inst Allergy & Immunol, Div Cellular Immunol, San Diego, CA 92121 USA