Evaluation of quantum dot immunofluorescence and a digital CMOS imaging system as an alternative to conventional organic fluorescence dyes and laser scanning for quantifying protein microarrays.
نویسندگان
چکیده
Organic fluorescent dyes are widely used for the visualization of bound antibody in a variety of immunofluorescence assays. However, the detection equipment is often expensive, fragile, and hard to deploy widely. Quantum dots (Qdot) are nanocrystals made of semiconductor materials that emit light at different wavelengths according to the size of the crystal, with increased brightness and stability. Here, we have evaluated a small benchtop "personal" optical imager (ArrayCAM) developed for quantification of protein arrays probed by Qdot-based indirect immunofluorescence. The aim was to determine if the Qdot imager system provides equivalent data to the conventional organic dye-labeled antibody/laser scanner system. To do this, duplicate proteome microarrays of Vaccinia virus, Brucella melitensis and Plasmodium falciparum were probed with identical samples of immune sera, and IgG, IgA, and IgM profiles visualized using biotinylated secondary antibodies followed by a tertiary reagent of streptavidin coupled to either P3 (an organic cyanine dye typically used for microarrays) or Q800 (Qdot). The data show excellent correlation for all samples tested (R > 0.8) with no significant change of antibody reactivity profiles. We conclude that Qdot detection provides data equivalent to that obtained using conventional organic dye detection. The portable imager offers an economical, more robust, and deployable alternative to conventional laser array scanners.
منابع مشابه
A fast wallace-based parallel multiplier in quantum-dot cellular automata
Physical limitations of Complementary Metal-Oxide-Semiconductors (CMOS) technology at nanoscale and high cost of lithography have provided the platform for creating Quantum-dot Cellular Automata (QCA)-based hardware. The QCA is a new technology that promises smaller, cheaper and faster electronic circuits, and has been regarded as an effective solution for scalability problems in CMOS technolog...
متن کاملA Novel Design of a Multi-layer 2:4 Decoder using Quantum- Dot Cellular Automata
The quantum-dot cellular automata (QCA) is considered as an alternative tocomplementary metal oxide semiconductor (CMOS) technology based on physicalphenomena like Coulomb interaction to overcome the physical limitations of thistechnology. The decoder is one of the important components in digital circuits, whichcan be used in more comprehensive circuits such as full adde...
متن کاملA fast wallace-based parallel multiplier in quantum-dot cellular automata
Physical limitations of Complementary Metal-Oxide-Semiconductors (CMOS) technology at nanoscale and high cost of lithography have provided the platform for creating Quantum-dot Cellular Automata (QCA)-based hardware. The QCA is a new technology that promises smaller, cheaper and faster electronic circuits, and has been regarded as an effective solution for scalability problems in CMOS technolog...
متن کاملFault-tolerant adder design in quantum-dot cellular automata
Quantum-dot cellular automata (QCA) are an emerging technology and a possible alternative for faster speed, smaller size, and low power consumption than semiconductor transistor based technologies. Previously, adder designs based on conventional designs were examined for implementation with QCA technology. This paper utilizes the QCA characteristics to design a fault-tolerant adder that is more...
متن کاملFault-tolerant adder design in quantum-dot cellular automata
Quantum-dot cellular automata (QCA) are an emerging technology and a possible alternative for faster speed, smaller size, and low power consumption than semiconductor transistor based technologies. Previously, adder designs based on conventional designs were examined for implementation with QCA technology. This paper utilizes the QCA characteristics to design a fault-tolerant adder that is more...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- Proteomics
دوره 16 8 شماره
صفحات -
تاریخ انتشار 2016