Single-molecule analysis of epidermal growth factor signaling that leads to ultrasensitive calcium response

被引:45
作者
Uyemura, T
Takagi, H
Yanagida, T
Sako, Y
机构
[1] Osaka Univ, Grad Sch Frontier Biosci, Labs Nanobiol, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Grad Sch Engn Sci, Dept Mech Sci & Bioengn, Suita, Osaka 5650871, Japan
关键词
D O I
10.1529/biophysj.104.053330
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Quantitative relationships between inputs and outputs of signaling systems are fundamental information for the understanding of the mechanism of signal transduction. Here we report the correlation between the number of epidermal growth factor (EGF) bindings and the response probability of intracellular calcium elevation. Binding of EGF molecules and changes of intracellular calcium concentration were measured for identical HeLa human epithelial cells. It was found that 300 molecules of EGF were enough to induce calcium response in half of the cells. This number is quite small compared to the number of EGF receptors ( EGFR) expressed on the cell surface ( 50,000). There was a sigmoidal correlation between the response probability and the number of EGF bindings, meaning an ultrasensitive reaction. Analysis of the cluster size distribution of EGF demonstrated that dimerization of EGFR contributes to this switch-like ultrasensitive response. Single-molecule analysis revealed that EGF bound faster to clusters of EGFR than to monomers. This property should be important for effective formation of signaling dimers of EGFR under very small numbers of EGF bindings and suggests that the expression of excess amounts of EGFR on the cell surface is required to prepare predimers of EGFR with a large association rate constant to EGF.
引用
收藏
页码:3720 / 3730
页数:11
相关论文
共 48 条
[1]   HIGH-AFFINITY EPIDERMAL GROWTH-FACTOR BINDING IS SPECIFICALLY REDUCED BY A MONOCLONAL-ANTIBODY, AND APPEARS NECESSARY FOR EARLY RESPONSES [J].
BELLOT, F ;
MOOLENAAR, W ;
KRIS, R ;
MIRAKHUR, B ;
VERLAAN, I ;
ULLRICH, A ;
SCHLESSINGER, J ;
FELDER, S .
JOURNAL OF CELL BIOLOGY, 1990, 110 (02) :491-502
[2]  
BERKERS JAM, 1991, J BIOL CHEM, V266, P922
[3]   INOSITOL TRISPHOSPHATE FORMATION AND CALCIUM MOBILIZATION IN SWISS 3T3 CELLS IN RESPONSE TO PLATELET-DERIVED GROWTH-FACTOR [J].
BERRIDGE, MJ ;
HESLOP, JP ;
IRVINE, RF ;
BROWN, KD .
BIOCHEMICAL JOURNAL, 1984, 222 (01) :195-201
[4]   MECHANISM OF EPIDERMAL GROWTH-FACTOR RECEPTOR AUTOPHOSPHORYLATION AND HIGH-AFFINITY BINDING [J].
BONISCHNETZLER, M ;
PILCH, PF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (22) :7832-7836
[5]   SIGNAL TRANSMISSION BY EPIDERMAL GROWTH-FACTOR RECEPTOR - COINCIDENCE OF ACTIVATION AND DIMERIZATION [J].
CANALS, F .
BIOCHEMISTRY, 1992, 31 (18) :4493-4501
[6]   EPIDERMAL GROWTH-FACTOR [J].
CARPENTER, G ;
COHEN, S .
ANNUAL REVIEW OF BIOCHEMISTRY, 1979, 48 :193-216
[7]   RECEPTORS FOR EPIDERMAL GROWTH-FACTOR AND OTHER POLYPEPTIDE MITOGENS [J].
CARPENTER, G .
ANNUAL REVIEW OF BIOCHEMISTRY, 1987, 56 :881-914
[8]  
CARRAWAY KL, 1989, J BIOL CHEM, V264, P8699
[9]   BINDING OF FLUORESCEINATED EPIDERMAL GROWTH-FACTOR TO A431 CELL SUBPOPULATIONS STUDIED USING A MODEL-INDEPENDENT ANALYSIS OF FLOW CYTOMETRIC FLUORESCENCE DATA [J].
CHATELIER, RC ;
ASHCROFT, RG ;
LLOYD, CJ ;
NICE, EC ;
WHITEHEAD, RH ;
SAWYER, WH ;
BURGESS, AW .
EMBO JOURNAL, 1986, 5 (06) :1181-1186
[10]   Tripping the switch fantastic: How a protein kinase cascade can convert graded inputs into switch-like outputs [J].
Ferrell, JE .
TRENDS IN BIOCHEMICAL SCIENCES, 1996, 21 (12) :460-466