Codon-optimized Gaussia luciferase cDNA for mammalian gene expression in culture and in vivo

被引:512
作者
Tannous, BA
Kim, DE
Fernandez, JL
Weissleder, R
Breakefield, XO
机构
[1] Massachusetts Gen Hosp, Ctr Mol Imaging Res, Dept Radiol, Charlestown, MA 02129 USA
[2] Massachusetts Gen Hosp, Dept Neurol, Charlestown, MA 02129 USA
[3] Harvard Univ, Sch Med, Neurosci Program, Boston, MA 02115 USA
关键词
D O I
10.1016/j.ymthe.2004.10.016
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
Photoproteins have played a major role in advancing our understanding of biological processes. A broader array of biocompatible, nontoxic, and novel reporters can serve to expand this potential. Here we describe the properties of a luciferase from the copepod marine organism Gaussia princeps. It is a monomeric protein composed of 185 aa (19.9 kDa) with a short coding sequence (555 bp) making it suitable for viral vectors. The humanized form of Gaussia luciferase (hGLuc) was efficiently expressed in mammalian cells following delivery by HSV-1 amplicon vectors. It was found to be nontoxic and naturally secreted, with flash bioluminescence characteristics similar to those of other coelenterazine luciferases. hGLuc generated over 1000-fold higher bioluminescent signal intensity from live cells together with their immediate environment and over 100-fold higher intensity from viable cells alone (not including secreted luciferase) or cell lysates, compared to humanized forms of firefly (hFLuc) and Renilla (hRLuc) luciferases expressed under similar conditions. Furthermore, hGLuc showed 200-fold higher signal intensity than hRLuc and intensity comparable to that of hFLuc in vivo under standard imaging conditions. Gaussia luciferase provides a sensitive means of imaging gene delivery and other events in living cells in culture and in vivo, with a unique combination of features including high signal intensity, secretion, and ATP independence, thus being able to report from the cells and their environment in real time.
引用
收藏
页码:435 / 443
页数:9
相关论文
共 34 条
  • [1] Optical imaging of Renilla luciferase reporter gene expression in living mice
    Bhaumik, S
    Gambhir, SS
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (01) : 377 - 382
  • [2] The use of resonance energy transfer in high-throughput screening: BRET versus FRET
    Boute, N
    Jockers, R
    Issad, T
    [J]. TRENDS IN PHARMACOLOGICAL SCIENCES, 2002, 23 (08) : 351 - 354
  • [3] A mutagenesis study of the putative luciferin binding site residues of firefly luciferase
    Branchini, BR
    Southworth, TL
    Murtiashaw, MH
    Boije, H
    Fleet, SE
    [J]. BIOCHEMISTRY, 2003, 42 (35) : 10429 - 10436
  • [4] NAPHTHYLLUCIFERIN AND QUINOLYLLUCIFERIN - GREEN AND RED-LIGHT EMITTING FIREFLY LUCIFERIN ANALOGS
    BRANCHINI, BR
    HAYWARD, MM
    BAMFORD, S
    BRENNAN, PM
    LAJINESS, EJ
    [J]. PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1989, 49 (05) : 689 - 695
  • [5] PHOTOPROTEINS AS INDICATORS OF INTRACELLULAR FREE CA-2+
    CAMPBELL, AK
    PATEL, A
    HOUSTON, WAJ
    SCOLDING, NJ
    FRITH, S
    MORGAN, BP
    COMPSTON, DAS
    [J]. JOURNAL OF BIOLUMINESCENCE AND CHEMILUMINESCENCE, 1989, 4 (01): : 463 - 474
  • [6] Chiu NHL, 1999, CLIN CHEM, V45, P1954
  • [7] Visualizing gene expression in living mammals using a bioluminescent reporter
    Contag, CH
    Spilman, SD
    Contag, PR
    Oshiro, M
    Eames, B
    Dennery, P
    Stevenson, DK
    Benaron, DA
    [J]. PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1997, 66 (04) : 523 - 531
  • [8] Advances in vivo bioluminescence imaging of gene expression
    Contag, CH
    Bachmann, MH
    [J]. ANNUAL REVIEW OF BIOMEDICAL ENGINEERING, 2002, 4 : 235 - 260
  • [9] DEWET JR, 1985, P NATL ACAD SCI USA, V82, P7870
  • [10] CRYSTALLINE FIREFLY LUCIFERASE
    GREEN, AA
    MCELROY, WD
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1956, 20 (01) : 170 - 176