Force profiles of protein pulling with or without cytoskeletal links studied by AFM

被引:29
作者
Afrin, Rehana [1 ]
Ikai, Atsushi [1 ]
机构
[1] Tokyo Inst Technol, Biodynam Lab, Dept Life Sci, Grad Sch Biosci & Biotechnol,Midori Ku, Yokohama, Kanagawa 2268501, Japan
基金
日本学术振兴会;
关键词
atomic force microscopy (AFM); red blood cell (RBC); glycophorin A (GLA); wheat germ agglutinin (WGA); Psathyrella velutina lectin (PVL); band; 3; protein; cytoskeleton; interaction force; lipid tether; concanavalin A (Con A);
D O I
10.1016/j.bbrc.2006.07.050
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
To test the capability of the atomic force microscope for distinguishing membrane proteins with/without cytoskeletal associations, we studied the pull-out mechanics of lipid tethers from the red blood cell (RBC). When wheat germ agglutinin, a glycophorin A (GLA) specific lectin, was used to pull out tethers from RBC, characteristic force curves for tether elongation having a long plateau force were observed but without force peaks which are usually attributed to the forced unbinding of membrane components from the cytoskeleton. The result was in agreement with the reports that GLA is substantially free of cytoskeletal interactions. On the contrary, when the Band 3 specific lectin, concanavalin A, was used, the force peaks were indeed observed together with a plateau supporting its reported cytoskeletal association. Based on these observations, we postulate that the state of cytoskeletal association of particular membrane proteins can be identified from the force profiles of their pull-out mechanics. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:238 / 244
页数:7
相关论文
共 34 条
[1]   Analysis of force curves obtained on the live cell membrane using chemically modified AFM probes (vol 100, pg 187, 2004) [J].
Afrin, R ;
Yamada, T ;
Ikai, A .
ULTRAMICROSCOPY, 2005, 103 (03) :253-253
[2]   Extraction of membrane proteins from a living cell surface using the atomic force microscope and covalent crosslinkers [J].
Afrin, R ;
Arakawa, H ;
Osada, T ;
Ikai, A .
CELL BIOCHEMISTRY AND BIOPHYSICS, 2003, 39 (02) :101-117
[3]   Phosphatidylinositol-4,5-biphosphate (PIP2) differentially regulates the interaction of human erythrocyte protein 4.1 (4.1R) with membrane proteins [J].
An, Xiuli ;
Zhang, Xihui ;
Debnath, Gargi ;
Baines, Anthony J. ;
Mohandas, Narla .
BIOCHEMISTRY, 2006, 45 (18) :5725-5732
[4]   Glycophorin A dimerization and band 3 interaction during erythroid membrane biogenesis: in vivo studies in human glycophorin A transgenic mice [J].
Auffray, I ;
Marfatia, S ;
de Jong, K ;
Lee, G ;
Huang, CH ;
Paszty, C ;
Tanner, MJA ;
Mohandas, N ;
Chasis, JA .
BLOOD, 2001, 97 (09) :2872-2878
[5]  
BELL GI, 1978, SCIENCE, V200, P618, DOI 10.1126/science.347575
[6]   Force measurements with the atomic force microscope: Technique, interpretation and applications [J].
Butt, HJ ;
Cappella, B ;
Kappl, M .
SURFACE SCIENCE REPORTS, 2005, 59 (1-6) :1-152
[7]   Identification of a critical ankyrin-binding loop on the cytoplasmic domain of erythrocyte membrane band 3 by crystal structure analysis and site-directed mutagenesis [J].
Chang, SH ;
Low, PS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (09) :6879-6884
[8]   ERYTHROCYTE-MEMBRANE RIGIDITY INDUCED BY GLYCOPHORIN-A LIGAND INTERACTION - EVIDENCE FOR A LIGAND-INDUCED ASSOCIATION BETWEEN GLYCOPHORIN-A AND SKELETAL PROTEINS [J].
CHASIS, JA ;
MOHANDAS, N ;
SHOHET, SB .
JOURNAL OF CLINICAL INVESTIGATION, 1985, 75 (06) :1919-1926
[9]  
CHASIS JA, 1992, BLOOD, V80, P1869
[10]   Regulation of band 3 rotational mobility by ankyrin in intact human red cells [J].
Cho, MR ;
Eber, SW ;
Liu, SC ;
Lux, SE ;
Golan, DE .
BIOCHEMISTRY, 1998, 37 (51) :17828-17835