Bifunctional antibody-Renilla luciferase fusion protein for in vivo optical detection of tumors

被引:44
|
作者
Venisnik, Katy M.
Olafsen, Tove
Loening, Andreas M.
Iyer, Meera
Gambhir, Sanjiv S.
Wu, Anna M.
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Mol & Med Pharmacol, Crump Inst Mol Imaging, Los Angeles, CA 90095 USA
[2] Stanford Univ, MIPS, Dept Radiol, Stanford, CA 94305 USA
[3] Stanford Univ, Bio X Program, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
来源
关键词
bioluminescence; carcinoembryonic antigen; engineered antibodies; nude mouse xenograft models; Renilla luciferase;
D O I
10.1093/protein/gzl030
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
An anti-carcinoembryonic antigen (CEA) antibody fragment, the anti-CEA diabody, was fused to the bioluminescence enzyme Renilla luciferase (RLuc) to generate a novel optical imaging probe. Native RLuc or one of two stabilized variants (RLucC124A, RLuc8) was used as the bioluminescent moiety. A bioluminescence ELISA showed that diabody-luciferase could simultaneously bind to CEA and emit light. In vivo optical imaging of tumor-bearing mice demonstrated specific targeting of diabody-RLuc8 to CEA-positive xenografts, with a tumor:background ratio of 6.0 +/- 0.8 at 6 h after intravenous injection, compared with antigen-negative tumors at 1.0 +/- 0.1 (P = 0.05). Targeting and distribution was also evaluated by microPET imaging using I-124-diabody-RLuc8 and confirmed that the optical signal was due to antibody-mediated localization of luciferase. Renilla luciferase, fused to biospecific sequences such as engineered antibodies, can be administered systemically to provide a novel, sensitive method for optical imaging based on expression of cell surface receptors in living organisms.
引用
收藏
页码:453 / 460
页数:8
相关论文
共 50 条
  • [1] Detecting protein-protein interactions using Renilla luciferase fusion proteins
    Burbelo, PD
    Kisailus, AE
    Peck, JW
    BIOTECHNIQUES, 2002, 33 (05) : 1044 - +
  • [2] The Renilla luciferase modified GFP fusion protein is functional in transformed cells
    Wang, Y
    Wang, G
    OKane, DJ
    Szalay, AA
    BIOLUMINESCENCE AND CHEMILUMINESCENCE: MOLECULAR REPORTING WITH PHOTONS, 1997, : 419 - 422
  • [3] Protein-DNA interaction-based detection of small molecules by employing Renilla luciferase fusion protein:: Quantitative and generic measurement of tetracyclines with a Renilla luciferase-tagged Tet repressor protein
    Pellinen, Teijo
    Rytkonen, Kalle
    Ristiniemi, Noora
    Karp, Matti
    Lamminmaki, Urpo
    ANALYTICAL BIOCHEMISTRY, 2006, 358 (02) : 301 - 303
  • [4] Visualizing and quantifying protein secretion using a Renilla luciferase-GFP fusion protein
    Liu, JX
    Wang, YB
    Szalay, AA
    Escher, A
    LUMINESCENCE, 2000, 15 (01) : 45 - 49
  • [6] Development of a homogeneous immunoassay system using protein A fusion fragmented Renilla luciferase
    Mie, Masayasu
    Ngo Phan Bich Thuy
    Kobatake, Eiry
    ANALYST, 2012, 137 (05) : 1085 - 1089
  • [7] The Renilla luciferase-modified GFP fusion protein is functional in transformed cells
    Wang, YB
    Wang, GF
    O'Kane, DJ
    Szalay, AA
    BIOHYDROGEN, 1998, : 493 - 499
  • [8] Quantification of dynamic protein complexes using Renilla luciferase fragment complementation applied to protein kinase A activities in vivo
    Stefan, E.
    Aquin, S.
    Berger, N.
    Landry, C. R.
    Nyfeler, B.
    Bouvier, M.
    Michnick, S. W.
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (43) : 16916 - 16921
  • [9] Fusion of Gaussia luciferase to an engineered anti-carcinoembryonic antigen (CEA) antibody for in vivo optical imaging
    Venisnik, Katy M.
    Olafsen, Tove
    Gambhir, Sanjiv S.
    Wu, Anna M.
    MOLECULAR IMAGING AND BIOLOGY, 2007, 9 (05) : 267 - 277
  • [10] Fusion of Gaussia Luciferase to an Engineered Anti-carcinoembryonic Antigen (CEA) Antibody for In Vivo Optical Imaging
    Katy M. Venisnik
    Tove Olafsen
    Sanjiv S. Gambhir
    Anna M. Wu
    Molecular Imaging and Biology, 2007, 9 : 267 - 277