Novel polymer substrates for SFM investigations of living cells, biological membranes, and proteins

被引:8
作者
Linder, A [1 ]
Weiland, U [1 ]
Apell, HJ [1 ]
机构
[1] Univ Konstanz, Dept Biol, D-78457 Constance, Germany
关键词
polymer substrates; goldfish oligodendrocytes; goldfish fibroblasts; goldfish epithelioma cells; mouse; 3T3; cells; bacteriorhodopsin; immobilization;
D O I
10.1006/jsbi.1999.4104
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
Extended studies were performed to prepare substrates for scanning force microscopy of biological samples with a surface roughness below 1 nn rms over an area of 500 x 500 nm(2). The substrate smoothness and the lack of tip obscuring material are indispensable in order to visualize detailed structures of membrane surfaces, particularly when scanning the lamellipodia. of mechanically sensitive goldfish glial cells where peripheral lamellipodia are only 20-30 nm in thickness. Appropriate substrates are poly(vinyl phenyl ketone) or furan polymers with corrugations of 0.3 and 0.15 mo rms, respectively, to which the growth-promoting protein laminin adsorbs directly with an acceptably increased roughness. Cells show normal growth behavior on these substrates and stick to the substrates in a stable fashion during several scans. Thus details of the membrane's surface may be resolved and are not obscured by the substrate texture. The uncoated furan polymer substrates are suitable for immobilization of membrane preparations such as purified membrane fragments containing bacteriorhodopsin or Na,K-ATPase and protein preparations such as antibodies. (C) 1999 Academic Press.
引用
收藏
页码:16 / 26
页数:11
相关论文
共 31 条
[1]  
Apell Hans-Juergen, 1993, P275
[2]   NA,K-ATPASE IN CRYSTALLINE FORM INVESTIGATED BY SCANNING FORCE MICROSCOPY [J].
APELL, HJ ;
COLCHERO, J ;
LINDER, A ;
MARTI, O ;
MLYNEK, J .
ULTRAMICROSCOPY, 1992, 42 :1133-1140
[3]   IDENTIFICATION OF ASTROCYTE-LIKE AND OLIGODENDROCYTE-LIKE CELLS OF GOLDFISH OPTIC NERVES IN CULTURE [J].
BASTMEYER, M ;
BECKMANN, M ;
NONA, SM ;
CRONLYDILLON, JR ;
STUERMER, CAO .
NEUROSCIENCE LETTERS, 1989, 101 (02) :127-132
[4]   SIMILARITIES AND DIFFERENCES BETWEEN FISH OLIGODENDROCYTES AND SCHWANN-CELLS IN-VITRO [J].
BASTMEYER, M ;
JESERICH, G ;
STUERMER, CAO .
GLIA, 1994, 11 (04) :300-314
[5]  
BASTMEYER M, 1991, J NEUROSCI, V11, P626
[6]   ATOMIC FORCE MICROSCOPE [J].
BINNIG, G ;
QUATE, CF ;
GERBER, C .
PHYSICAL REVIEW LETTERS, 1986, 56 (09) :930-933
[7]   IMAGING THE MEMBRANE-PROTEIN BACTERIORHODOPSIN WITH THE ATOMIC FORCE MICROSCOPE [J].
BUTT, HJ ;
DOWNING, KH ;
HANSMA, PK .
BIOPHYSICAL JOURNAL, 1990, 58 (06) :1473-1480
[8]  
DALY WH, 1987, ENCY POLYM SCI ENG, V17, P548
[9]   Cytoplasmic topography of focal contacts [J].
Dunlap, D ;
Cattelino, A ;
deCurtis, I ;
Valtorta, F .
FEBS LETTERS, 1996, 382 (1-2) :65-72
[10]  
GANDINI A, 1986, ENCY POLYM SCI ENG, V7, P454