Use of nanogold and fluorescent-labeled antibody Fv fragments in immunocytochemistry

被引:37
作者
Ribrioux, S [1 ]
Kleymann, G [1 ]
Haase, W [1 ]
Heitmann, K [1 ]
Ostermeier, C [1 ]
Michel, H [1 ]
机构
[1] MAX PLANCK INST BIOPHYS,ABT MOLEK MEMBRANBIOL,D-60528 FRANKFURT,GERMANY
关键词
engineered antibody fragments; electron microscopy; nanogold labeling; fluorescence labeling; membrane protein; Paracoccus denitrificans; cytochrome C oxidase; ubiquinol:cytochrome c oxidoreductase; Halobacterium halobium; bacteriorhodopsin;
D O I
10.1177/44.3.8648079
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Recombinant antibody fragments are emerging as a versatile tool in both basic research and medical therapy. We describe the procedures for direct labeling of engineered antibody fragments (Fv) with fluorescein or nanogold and their use in fluorescence and immunoelectron microscopy, respectively. The Fv fragments were produced in Escherichia coli, purified by one-step Strep tag affinity chromatography, chemically labeled with the marker, and employed in microscopy to localize epitopes on the membrane protein bacteriorhodopsin in purple membranes of Halobacterium halobium and the cytochrome c oxidase of Paracoccus denitrificans. In both cases, methods involving directly labeled antibody fragments show results identical to those in which antibodies or Iv fragments are detected by a secondarily labeled conjugate. The multifunctional design of the recombinant Iv fragments, however, offers more all-around applications in immunocytochemistry, The directly labeled Iv fragments, half the size of an Fab fragment, are at the molecular level the smallest antibody fragments yet described for visualization of biomolecules in microscopy.
引用
收藏
页码:207 / 213
页数:7
相关论文
共 31 条
[1]   ESCHERICHIA-COLI SECRETION OF AN ACTIVE CHIMERIC ANTIBODY FRAGMENT [J].
BETTER, M ;
CHANG, CP ;
ROBINSON, RR ;
HORWITZ, AH .
SCIENCE, 1988, 240 (4855) :1041-1043
[2]   SINGLE-CHAIN ANTIGEN-BINDING PROTEINS [J].
BIRD, RE ;
HARDMAN, KD ;
JACOBSON, JW ;
JOHNSON, S ;
KAUFMAN, BM ;
LEE, SM ;
LEE, T ;
POPE, SH ;
RIORDAN, GS ;
WHITLOW, M .
SCIENCE, 1988, 242 (4877) :423-426
[3]  
Coons AH, 1941, P SOC EXP BIOL MED, V47, P200, DOI 10.3181/00379727-47-13084P
[4]   MAMMALIAN-CELL EXPRESSION OF SINGLE-CHAIN FV (SFV) ANTIBODY PROTEINS AND THEIR C-TERMINAL FUSIONS WITH INTERLEUKIN-2 AND OTHER EFFECTOR DOMAINS [J].
DORAI, H ;
MCCARTNEY, JE ;
HUDZIAK, RM ;
TAI, MS ;
LAMINET, AA ;
HOUSTON, LL ;
HUSTON, JS ;
OPPERMANN, H .
BIO-TECHNOLOGY, 1994, 12 (09) :890-897
[5]  
FAULK WP, 1971, IMMUNOCHEMISTRY, V8, P1081
[6]   USE OF COLLOIDAL GOLD FOR STUDIES OF INTRACELLULAR EXCHANGES IN AMEBA CHAOS CHAOS [J].
FELDHERR, CM ;
MARSHALL, JM .
JOURNAL OF CELL BIOLOGY, 1962, 12 (03) :640-&
[7]   CALCULATION OF PROTEIN EXTINCTION COEFFICIENTS FROM AMINO-ACID SEQUENCE DATA [J].
GILL, SC ;
VONHIPPEL, PH .
ANALYTICAL BIOCHEMISTRY, 1989, 182 (02) :319-326
[8]  
Griffiths G., 1993, FINE STRUCTURE IMMUN
[9]   A SMALL GOLD-CONJUGATED ANTIBODY LABEL - IMPROVED RESOLUTION FOR ELECTRON-MICROSCOPY [J].
HAINFELD, JF .
SCIENCE, 1987, 236 (4800) :450-453
[10]   A 1.4-NM GOLD CLUSTER COVALENTLY ATTACHED TO ANTIBODIES IMPROVES IMMUNOLABELING [J].
HAINFELD, JF ;
FURUYA, FR .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1992, 40 (02) :177-184