Anti-actin antibodies generated against profilin: actin distinguish between non-filamentous and filamentous actin, and label cultured cells in a dotted pattern

被引:18
作者
Grenklo, S [1 ]
Johansson, T [1 ]
Bertilson, L [1 ]
Karlsson, R [1 ]
机构
[1] Stockholm Univ, Dept Cell Biol, WGI, S-10691 Stockholm, Sweden
关键词
profilin-actin; antibodies; fluorescence microscopy; immunohistochemistry; microfilament dynamics;
D O I
10.1078/0171-9335-00400
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Actin polymerization is a prominent feature of migrating cells, where it powers the protrusion of the leading edge. Many studies have characterized the well-ordered and dynamic arrangement of filamentous actin in this submembraneous space. However, less is known about the organization of unpolymerized actin. Previously, we reported on the use of covalently coupled profilin:actin to study actin dynamics and presented evidence that profilin-bound actin is a major source of actin for filament growth. To locate profilin:actin in the cell we have now used this non-dissociable complex for antibody generation, and obtained monospecific anti-actin and antiprofilin antibodies from two separate immunizations. Fluorescence microscopy revealed drastic differences in the staining pattern generated by the anti-actin antibody preparations. With one, distinct puncta appeared at the actin-rich leading edge and sometimes aligned with microtubules in the interior of the lamella, while the other displayed typical actin filament staining. Labelling experiments in vitro demonstrated failure of the first antibody to recognize filamentous actin and none of the two bound microtubules. The two anti-profilin antibodies purified in parallel generated a punctated pattern similar to that seen with the first anti-actin antibody. All antibody preparations labelled the nuclei.
引用
收藏
页码:413 / 423
页数:11
相关论文
共 49 条
[1]   INTERFERENCE WITH MYOSIN SUBFRAGMENT-1 BINDING BY SITE-DIRECTED MUTAGENESIS OF ACTIN [J].
ASPENSTROM, P ;
KARLSSON, R .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1991, 200 (01) :35-41
[2]  
Ballestrem C, 1998, J CELL SCI, V111, P1649
[3]   Myosin-X is an unconventional myosin that undergoes intrafilopodial motility [J].
Berg, JS ;
Cheney, RE .
NATURE CELL BIOLOGY, 2002, 4 (03) :246-250
[4]   Opinion - Actin up in the nucleus [J].
Bettinger, BT ;
Gilbert, DM ;
Amberg, DC .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2004, 5 (05) :410-415
[5]   MUTAGENESIS OF HUMAN PROFILIN LOCATES ITS POLY(L-PROLINE)-BINDING SITE TO A HYDROPHOBIC PATCH OF AROMATIC-AMINO-ACIDS [J].
BJORKEGREN, C ;
ROZYCKI, M ;
SCHUTT, CE ;
LINDBERG, U ;
KARLSSON, R .
FEBS LETTERS, 1993, 333 (1-2) :123-126
[6]   DISTRIBUTION OF PROFILIN IN FIBROBLASTS CORRELATES WITH THE PRESENCE OF HIGHLY DYNAMIC ACTIN-FILAMENTS [J].
BUSS, F ;
TEMMGROVE, C ;
HENNING, S ;
JOCKUSCH, BM .
CELL MOTILITY AND THE CYTOSKELETON, 1992, 22 (01) :51-61
[7]   LOCALIZATION AND DYNAMICS OF NONFILAMENTOUS ACTIN IN CULTURED-CELLS [J].
CAO, LG ;
FISHKIND, DJ ;
WANG, YL .
JOURNAL OF CELL BIOLOGY, 1993, 123 (01) :173-181
[8]  
CASTRILLON DH, 1994, DEVELOPMENT, V120, P3367
[9]   CRYSTALLIZATION AND STRUCTURE DETERMINATION OF BOVINE PROFILIN AT 2-CENTER-DOT-0 ANGSTROM RESOLUTION [J].
CEDERGRENZEPPEZAUER, ES ;
GOONESEKERE, NCW ;
ROZYCKI, MD ;
MYSLIK, JC ;
DAUTER, Z ;
LINDBERG, U ;
SCHUTT, CE .
JOURNAL OF MOLECULAR BIOLOGY, 1994, 240 (05) :459-475
[10]   The structure of an open state of beta-actin at 2.65 angstrom resolution [J].
Chik, JK ;
Lindberg, U ;
Schutt, CE .
JOURNAL OF MOLECULAR BIOLOGY, 1996, 263 (04) :607-623