Cell Labeling via Membrane-Anchored Lipophilic MR Contrast Agents
Author(s) -
Christiane E. Carney,
Keith W. MacRenaris,
Daniel J. Mastarone,
David R. Kasjanski,
Andy H. Hung,
Thomas J. Meade
Publication year - 2014
Publication title -
bioconjugate chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.279
H-Index - 172
eISSN - 1520-4812
pISSN - 1043-1802
DOI - 10.1021/bc500083t
Subject(s) - chemistry , internalization , in vitro , cell , biophysics , hela , chelation , in vivo , membrane , cell membrane , lipid bilayer fusion , biochemistry , microbiology and biotechnology , organic chemistry , biology
Cell tracking in vivo with MR imaging requires the development of contrast agents with increased sensitivity that effectively label and are retained by cells. Most clinically approved Gd(III)-based contrast agents require high incubation concentrations and prolonged incubation times for cellular internalization. Strategies to increase contrast agent permeability have included conjugating Gd(III) complexes to cell penetrating peptides, nanoparticles, and small molecules which have greatly improved cell labeling but have not resulted in improved cellular retention. To overcome these challenges, we have synthesized a series of lipophilic Gd(III)-based MR contrast agents that label cell membranes in vitro. Two of the agents were synthesized with a multiplexing strategy to contain three Gd(III) chelates (1 and 2) while the third contains a single Gd(III) chelate (3). These new agents exhibit significantly enhanced labeling and retention in HeLa and MDA-MB-231-mcherry cells compared to agents that are internalized by cells (4 and Prohance).
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