Chemical Re-engineering of Chlorotoxin Improves Bioconjugation Properties for Tumor Imaging and Targeted Therapy

被引:71
作者
Akcan, Muharrem [4 ]
Stroud, Mark R. [1 ]
Hansen, Stacey J. [1 ]
Clark, Richard J. [4 ]
Daly, Norelle L. [4 ]
Craik, David J. [4 ]
Olson, James M. [1 ,2 ,3 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98109 USA
[2] Univ Washington, Dept Pediat, Seattle, WA 98105 USA
[3] Seattle Childrens Hosp, Seattle, WA 98105 USA
[4] Univ Queensland, Inst Mol Biosci, Brisbane, Qld 4072, Australia
基金
英国医学研究理事会;
关键词
BACKBONE CYCLIZATION; CONOTOXIN; SCORPION; PEPTIDE; GLIOMAS; POTENT; CELLS; MODEL; VENOM; NMR;
D O I
10.1021/jm101018r
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Bioconjugates composed of chlorotoxin and near-infrared fluorescent (NIRF) moieties are being advanced toward human clinical trials as intraoperative imaging agents that will enable surgeons to visualize small foci of cancer. In previous studies, the NIRF molecules were conjugated to chlorotoxin, which results in a mixture of mono-, di-, and trilabeled peptide. Here we report a new chemical entity that bound only a single NIRF molecule. The lysines at positions 15 and 23 were substituted with either alanine or argininc, which resulted in only monolabeled peptide that was functionally equivalent to native chlorotoxin/Cy5.5. We also analyzed the serum stability and serum half-life of cyclized chlorotoxin, which showed an 11 h serum half-life and resulted in a monolabeled product. Based on these data, we propose to advance a monolabeled chlorotoxin to human clinical trials.
引用
收藏
页码:782 / 787
页数:6
相关论文
共 31 条
  • [1] [Anonymous], 1986, NMR of proteins and nucleic acids
  • [2] Establishing Regiocontrol of Disulfide Bond Isomers of α-Conotoxin ImI via the Synthesis of N-to-C Cyclic Analogs
    Armishaw, Christopher J.
    Dutton, Julie L.
    Craik, David J.
    Alewood, Paul F.
    [J]. BIOPOLYMERS, 2010, 94 (03) : 307 - 313
  • [3] Camarero JA, 1998, ANGEW CHEM INT EDIT, V37, P347, DOI 10.1002/(SICI)1521-3773(19980216)37:3<347::AID-ANIE347>3.0.CO
  • [4] 2-5
  • [5] Chemoselective backbone cyclization of unprotected peptides
    Camarero, JA
    Muir, TW
    [J]. CHEMICAL COMMUNICATIONS, 1997, (15) : 1369 - 1370
  • [6] The Engineering of an Orally Active Conotoxin for the Treatment of Neuropathic Pain
    Clark, Richard J.
    Jensen, Jonas
    Nevin, Simon T.
    Callaghan, Brid P.
    Adams, David J.
    Craik, David J.
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2010, 49 (37) : 6545 - 6548
  • [7] Engineering stable peptide toxins by means of backbone cyclization:: Stabilization of the α-conotoxin MII
    Clark, RJ
    Fischer, H
    Dempster, L
    Daly, NL
    Rosengren, KJ
    Nevin, ST
    Meunier, FA
    Adams, DJ
    Craik, DJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (39) : 13767 - 13772
  • [8] Discovery, structure and biological activities of cyclotides
    Daly, Norelle L.
    Rosengren, K. Johan
    Craik, David J.
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 2009, 61 (11) : 918 - 930
  • [9] SYNTHESIS OF PROTEINS BY NATIVE CHEMICAL LIGATION
    DAWSON, PE
    MUIR, TW
    CLARKLEWIS, I
    KENT, SBH
    [J]. SCIENCE, 1994, 266 (5186) : 776 - 779
  • [10] PURIFICATION AND CHARACTERIZATION OF CHLOROTOXIN, A CHLORIDE CHANNEL LIGAND FROM THE VENOM OF THE SCORPION
    DEBIN, JA
    MAGGIO, JE
    STRICHARTZ, GR
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (02): : C361 - C369