Positively charged DNA-binding proteins cause apparent cell membrane translocation

被引:202
作者
Lundberg, M
Johansson, M [1 ]
机构
[1] Huddinge Univ Hosp, Karolinska Inst, Div Clin Virol F68, S-14186 Huddinge, Sweden
[2] Karolinska Inst, Dept Med Biochem & Biophys, Med Nobel Inst Biochem, S-17177 Stockholm, Sweden
关键词
protein transduction domain; protein delivery; gene therapy; membrane translocation; immunocytochemistry; protein therapeutics;
D O I
10.1006/bbrc.2002.6450
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Several positively charged DNA-binding proteins such as the human immunodeficiency virus Tat protein, the Antennapedia (Antp) homeobox protein, and the herpes simplex virus VP22 protein have been reported to translocate across cell membranes and accumulate in cell nuclei. The import occurs by a poorly understood mechanism that appears to be receptor- and energy-independent. We showed that both VP22 and the positively charged histone H1 adhered to the cell membrane of living cells and were not removed by extensive washing. However, after fixation the proteins relocated to the cell nucleus. The nuclear accumulation of VP22 and histone HI after fixation shows that positively charged proteins may appear to translocate across the cell membrane because of a fixation artifact. The majority of studies on "membrane permeable" proteins and peptides have been performed using fixation techniques, and our study shows that influx of these proteins may occur during fixation rather than in living cells. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:367 / 371
页数:5
相关论文
共 24 条
[11]   Arginine-rich peptides - An abundant source of membrane-permeable peptides having potential as carriers for intracellular protein delivery [J].
Futaki, S ;
Suzuki, T ;
Ohashi, W ;
Yagami, T ;
Tanaka, S ;
Ueda, K ;
Sugiura, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (08) :5836-5840
[12]  
Ho A, 2001, CANCER RES, V61, P474
[13]   Conformational lability of herpesvirus protein VP22 [J].
Kueltzo, LA ;
Normand, N ;
O'Hare, P ;
Middaugh, CR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (43) :33213-33221
[14]   Tat peptide-derivatized magnetic nanoparticles allow in vivo tracking and recovery of progenitor cells [J].
Lewin, M ;
Carlesso, N ;
Tung, CH ;
Tang, XW ;
Cory, D ;
Scadden, DT ;
Weissleder, R .
NATURE BIOTECHNOLOGY, 2000, 18 (04) :410-414
[15]   Is VP22 nuclear homing an artifact? [J].
Lundberg, M ;
Johansson, M .
NATURE BIOTECHNOLOGY, 2001, 19 (08) :713-713
[16]   Transduction of full-length TAT fusion proteins into mammalian cells:: TAT-p27Kip1 induces cell migration [J].
Nagahara, H ;
Vocero-Akbani, AM ;
Snyder, EL ;
Ho, A ;
Latham, DG ;
Lissy, NA ;
Becker-Hapak, M ;
Ezhevsky, SA ;
Dowdy, SF .
NATURE MEDICINE, 1998, 4 (12) :1449-1452
[17]   Intercellular delivery of functional p53 by the herpesvirus protein VP22 [J].
Phelan, A ;
Elliott, G ;
O'Hare, P .
NATURE BIOTECHNOLOGY, 1998, 16 (05) :440-443
[18]   A 16-mer peptide (RQIKIWFQNRRMKWKK) from antennapedia preferentially targets the Class I pathway [J].
Pietersz, GA ;
Li, WJ ;
Apostolopoulos, V .
VACCINE, 2001, 19 (11-12) :1397-1405
[19]   Protein transduction: unrestricted delivery into all cells? [J].
Schwarze, SR ;
Hruska, KA ;
Dowdy, SF .
TRENDS IN CELL BIOLOGY, 2000, 10 (07) :290-295
[20]   In vivo protein transduction: Delivery of a biologically active protein into the mouse [J].
Schwarze, SR ;
Ho, A ;
Vocero-Akbani, A ;
Dowdy, SF .
SCIENCE, 1999, 285 (5433) :1569-1572