A galinstan expansion femtosyringe for microinjection of eukaryotic organelles and prokaryotes

被引:122
作者
Knoblauch, M
Hibberd, JM
Gray, JC
van Bel, AJE
机构
[1] Univ Giessen, Inst Gen Bot & Plant Physiol, D-35390 Giessen, Germany
[2] Univ Cambridge, Dept Plant Sci, Cambridge CB2 3EA, England
关键词
microinjection; galinstan expansion femtosyringe; green fluorescent protein; chloroplast; cyanobacteria; transformation;
D O I
10.1038/12902
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A galinstan expansion femtosyringe enables femtoliter to attoliter samples to be introduced into prokaryotes and subcellular compartments of eukaryotes. The method uses heat-induced expansion of galinstan (a liquid metal alloy of gallium, indium, and tin) within a glass syringe to expel samples through a tip diameter of about 0.1 mu m. The narrow tip inflicts less damage than conventional capillaries, and the heat-induced expansion of the galinstan allows fine control over the rate of injection. We demonstrate injection of Lucifer Yellow and Lucifer Yellow-dextran conjugates into cyanobacteria, and into nuclei and chloroplasts of higher organisms. Injection of a plasmid containing the bla gene into the cyanobacterium Phormidium laminosum resulted in transformed ampiciltin-resistant cultures. Green fluorescent protein was expressed in attached leaves of tobacco and Vicia faba following injection of DNA cantaining its gene into individual chloroplasts.
引用
收藏
页码:906 / 909
页数:4
相关论文
共 26 条
[1]  
DANIELL H, 1991, PLANT CELL REP, V9, P615, DOI 10.1007/BF00231800
[2]   TRANSIENT FOREIGN GENE-EXPRESSION IN CHLOROPLASTS OF CULTURED TOBACCO CELLS AFTER BIOLISTIC DELIVERY OF CHLOROPLAST VECTORS [J].
DANIELL, H ;
VIVEKANANDA, J ;
NIELSEN, BL ;
YE, GN ;
TEWARI, KK ;
SANFORD, JC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (01) :88-92
[3]   STABLE PLASTID TRANSFORMATION IN PEG-TREATED PROTOPLASTS OF NICOTIANA-TABACUM [J].
GOLDS, T ;
MALIGA, P ;
KOOP, HU .
BIO-TECHNOLOGY, 1993, 11 (01) :95-97
[4]   Green-fluorescent protein fusions for efficient characterization of nuclear targeting [J].
Grebenok, RJ ;
Pierson, E ;
Lambert, GM ;
Gong, FC ;
Afonso, CL ;
HaldemanCahill, R ;
Carrington, JC ;
Galbraith, DW .
PLANT JOURNAL, 1997, 11 (03) :573-586
[5]  
HANDLER JS, 1981, AM J PHYSIOL, V240, P103
[6]   Removal of a cryptic intron and subcellular localization of green fluorescent protein are required to mark transgenic Arabidopsis plants brightly [J].
Haseloff, J ;
Siemering, KR ;
Prasher, DC ;
Hodge, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (06) :2122-2127
[7]   A complex containing N-CoR, mSin3 and histone deacetylase mediates transcriptional repression [J].
Heinzel, T ;
Lavinsky, RM ;
Mullen, TM ;
Soderstrom, M ;
Laherty, CD ;
Torchia, J ;
Yang, WM ;
Brard, G ;
Ngo, SD ;
Davie, JR ;
Seto, E ;
Eisenman, RN ;
Rose, DW ;
Glass, CK ;
Rosenfeld, MG .
NATURE, 1997, 387 (6628) :43-48
[8]   Transient expression of green fluorescent protein in various plastid types following microprojectile bombardment [J].
Hibberd, JM ;
Linley, PJ ;
Khan, MS ;
Gray, JC .
PLANT JOURNAL, 1998, 16 (05) :627-632
[9]   MODULATION OF CELLULAR MORPHOLOGY AND LOCOMOTORY ACTIVITY BY ANTIBODIES AGAINST MYOSIN [J].
HONER, B ;
CITI, S ;
KENDRICKJONES, J ;
JOCKUSCH, BM .
JOURNAL OF CELL BIOLOGY, 1988, 107 (06) :2181-2189
[10]   A CBP integrator complex mediates transcriptional activation and AP-1 inhibition by nuclear receptors [J].
Kamei, Y ;
Xu, L ;
Heinzel, T ;
Torchia, J ;
Kurokawa, R ;
Gloss, B ;
Lin, SC ;
Heyman, RA ;
Rose, DW ;
Glass, CK ;
Rosenfeld, MG .
CELL, 1996, 85 (03) :403-414