Reduced protein diffusion rate by cytoskeleton in vegetative and polarized Dictyostelium cells

被引:98
作者
Potma, EO
de Boeij, WP
Bosgraaf, L
Roelofs, J
van Haastert, PJM
Wiersma, DA
机构
[1] Univ Groningen, Groningen Biomol Sci & Biotechnol Inst, NL-9747 AG Groningen, Netherlands
[2] Univ Groningen, Ultrafast Laser & Spect Lab, Ctr Mat Sci, NL-9747 AG Groningen, Netherlands
关键词
D O I
10.1016/S0006-3495(01)75851-1
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Fluorescence recovery after photobleaching measurements with high spatial resolution are performed to elucidate the impact of the actin cytoskeleton on translational mobility of green fluorescent protein (GFP) in aqueous domains of Dictyostelium discoideum amoebae. In vegetative Dictyostelium cells, GFP molecules experience a 3.6-fold reduction of their translational mobility relative to dilute aqueous solutions. In disrupting the actin filamentous network using latrunculin-A, the intact actin cytoskeletal network is shown to contribute an effective viscosity of 1.36 cP, which accounts for 53% of the restrained molecular diffusion of GFP. The remaining 47% of hindered protein motions is ascribed to other mechanical barriers and the viscosity of the cell liquid. A direct correlation between the density of the actin network and its limiting action on protein diffusion is furthermore established from measurements under different osmotic conditions. In highly locomotive polarized cells, the obstructing effect of the actin filamentous network is seen to decline to 0.46 cP in the non-cortical regions of the cell. Our results indicate that the meshwork of actin filaments constitutes the primary mechanical barrier for protein diffusion and that any noticeable reorganization of the network is accompanied by altered intracellular protein mobility.
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收藏
页码:2010 / 2019
页数:10
相关论文
共 37 条
[1]   MOBILITY MEASUREMENT BY ANALYSIS OF FLUORESCENCE PHOTOBLEACHING RECOVERY KINETICS [J].
AXELROD, D ;
KOPPEL, DE ;
SCHLESSINGER, J ;
ELSON, E ;
WEBB, WW .
BIOPHYSICAL JOURNAL, 1976, 16 (09) :1055-1069
[2]   High rates of actin filament turnover in budding yeast and roles for actin in establishment and maintenance of cell polarity revealed using the actin inhibitor latrunculin-A [J].
Ayscough, KR ;
Stryker, J ;
Pokala, N ;
Sanders, M ;
Crews, P ;
Drubin, DG .
JOURNAL OF CELL BIOLOGY, 1997, 137 (02) :399-416
[3]   FLUORESCENCE PHOTOBLEACHING RECOVERY IN THE CONFOCAL SCANNING LIGHT-MICROSCOPE [J].
BLONK, JCG ;
DON, A ;
VANAALST, H ;
BIRMINGHAM, JJ .
JOURNAL OF MICROSCOPY-OXFORD, 1993, 169 :363-374
[4]   ACTIN CONTENT OF FIBROBLASTS [J].
BRAY, D ;
THOMAS, C .
BIOCHEMICAL JOURNAL, 1975, 147 (02) :221-+
[5]  
BRINKMAN HC, 1947, APPL SCI RES, V1, P27
[6]   Measurement of molecular diffusion in solution by multiphoton fluorescence photobleaching recovery [J].
Brown, EB ;
Wu, ES ;
Zipfel, W ;
Webb, WW .
BIOPHYSICAL JOURNAL, 1999, 77 (05) :2837-2849
[7]   LIFE AT THE LEADING-EDGE - THE FORMATION OF CELL PROTRUSIONS [J].
CONDEELIS, J .
ANNUAL REVIEW OF CELL BIOLOGY, 1993, 9 :411-444
[8]   THE ROLE OF ACTIN POLYMERIZATION IN CELL MOTILITY [J].
COOPER, JA .
ANNUAL REVIEW OF PHYSIOLOGY, 1991, 53 :585-605
[9]   NEW HORIZONS FOR CYTOKINESIS [J].
FISHKIND, DJ ;
WANG, YL .
CURRENT OPINION IN CELL BIOLOGY, 1995, 7 (01) :23-31
[10]   Real-time light-driven dynamics of the fluorescence emission in single green fluorescent protein molecules [J].
Garcia-Parajo, MF ;
Segers-Nolten, GMJ ;
Veerman, JA ;
Greve, J ;
van Hulst, NF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (13) :7237-7242