Polymer-based elemental tags for sensitive bioassays.

To identify a rare (e.g., diseased or foreign) cell in a complex mixture, or to understand the proteomic complexity[1,2] of cells, one needs to be able to measure simultaneously and quantitatively a large number of proteins or other biomarkers that may be present in a complex sample. This is a difficult task and is beyond the reach of current capabilities. To address a problem of this complexity, we have begun to develop a high-sensitivity assay[3–6] based upon elemental tags that will enable the simultaneous measurement of many proteins in a single sample. The advantage of this approach lies in the large number of available elements and isotopes (potentially greater than 79) found in low abundance in biological systems, which will allow multiple tags to be used simultaneously. Inductively coupled plasma mass spectrometry (ICP-MS) is an ideal technique for detecting and quantifying these tags, as ICP-MS provides excellent resolution between the tag masses and an exceptional dynamic range (nine orders of magnitude).[7] This method allows one to overcome some of the limitations of currently available fluorescent tagging approaches.[8] These limitations arise from the spectral overlap of different dyes and the difficulty in measuring simultaneously targets that differ in abundance by an order of magnitude or more. Other benefits of ICP-MS detection include the high sensitivity, which is comparable to that of radioimmunoassays or chemiluminescent assays,[3] insensitivity of elemental tags to photobleaching and storage time, as well as the stability of the tagged sample so that it can be stored or shipped for analysis. We discuss herein the development of a new class of elemental tags for ICP-MS detection and their use for tagging of antibodies chosen to allow specific recognition of distinguishing cell surface markers. By using this technique it should be possible to achieve detection limits on the order of parts per billion, which will allow the detection of cell surface markers with copy numbers as low as 100.

[1]  S. Tanner,et al.  Simultaneous determination of proteins using an element-tagged immunoassay coupled with ICP-MS detection , 2002 .

[2]  O. Ornatsky,et al.  Multiple cellular antigen detection by ICP-MS. , 2006, Journal of immunological methods.

[3]  C. McCormick,et al.  Fluorescent labeling of RAFT-generated poly(N-isopropylacrylamide) via a facile maleimide-thiol coupling reaction. , 2006, Biomacromolecules.

[4]  J. Barton DNA-mediated electron transfer: Chemistry at a distance , 1998 .

[5]  T. Okano,et al.  Polymer terminal group effects on properties of thermoresponsive polymeric micelles with controlled outer-shell chain lengths. , 2005, Biomacromolecules.

[6]  S. Tanner,et al.  Reaction cells and collision cells for ICP-MS: a tutorial review , 2002 .

[7]  S. Tanner,et al.  The potential for elemental analysis in biotechnology , 2002 .

[8]  C. Geraldes,et al.  Lanthanide(III) complexes of DOTA-glycoconjugates: a potential new class of lectin-mediated medical imaging agents. , 2004, Chemistry.

[9]  Ruth Etzioni,et al.  Early detection: The case for early detection , 2003, Nature Reviews Cancer.

[10]  C. Pichot,et al.  Well-defined polymer precursors synthesized by RAFT polymerization of N,N-dimethylacrylamide/N-acryloxysuccinimide: random and block copolymers , 2004 .

[11]  Horst Puschmann,et al.  Being excited by lanthanide coordination complexes: aqua species, chirality, excited-state chemistry, and exchange dynamics. , 2002, Chemical reviews.

[12]  P. Chattopadhyay,et al.  Seventeen-colour flow cytometry: unravelling the immune system , 2004, Nature Reviews Immunology.

[13]  S. Tanner,et al.  A sensitive and quantitative element-tagged immunoassay with ICPMS detection. , 2002, Analytical chemistry.