A s the human genome project has uncovered the full sequence of human genomes and the postgenome technologies have been rapidly developed, DNA hybridization detection has become increasingly important. 1 A variety of DNA detection formats are now available, including both heterogeneous assays with surface-bound array-based probes and homogeneous solution-based detection schemes. 2 A number of those rely on fluorescence signal and, in particular, on fluorescence (or Fö rster) resonant energy transfer (FRET). 3 Both conjugated polymers and semiconductor nanocrystals (colloidal quantum dots, QDs) have been suggested for use as fluorescent entities in DNA detection assays. 4Ϫ12 Assays based on watersoluble cationic conjugated polymers allow one to utilize a simple binding strategy to DNA through electrostatic interactions with ionic side groups and benefit from the lightharvesting properties along the polymer backbone. 4Ϫ8 QDs have been increasingly used as donors in FRET-related studies, including optical DNA diagnostics. 9Ϫ12 QDs are photostable, highly efficient fluorophores with a strong band gap luminescence tunable by size as a result of the quantum confinement effect. 13 FRET in QD/ DNA/organic dye conjugates has been used to study DNA hybridization, 14,15 cleavage, 16 and replication. 17 Most of the reported approaches required covalent conjugation of DNA to the QD surface (e.g., by EDC/NHS coupling reaction), which often decreases the colloidal stability and/or the emission intensity of QDs. 18,19 This limitation can be overcome by the use of a sensing platform relying on the electrostatic interaction of dye-labeled DNA with the oppositely charged QD surface 20 in a similar fashion as in conducting polymer-based detection assays. 4Ϫ8 In this paper, we propose a simultaneous use of conjugated polymers and semiconductor QDs for DNA hybridization detection, which can potentially combine advantages of both light-harvesting and DNA-binding properties of water-soluble polymers with photostability, lightharvesting ability, and FRET donor property of QDs. A blue-emitting conjugated polymer with positively charged side chains electrostatically self-assembles on the negatively charged surface of red-emitting CdTe QDs. The so-formed hybrid complex has a net positive charge and thus attracts negatively charged dye-labeled DNA molecules (Scheme 1). The water-soluble, cationic, conjugated polymer, poly[9,9-bis(3=-((N,N-