DNA-NANO-AB · “DNA-based NANOdevices for the point-of-care electrochemical detection of AntiBodies”
Horizon 2020 — Marie Skłodowska-Curie Actions
- Duration
- 2020-03-01 → 2023-02-28
- EU contribution
- €251,003
- Participants
- 2
- Scheme
- MSCA-IF
Lines connect the coordinator with its partners.
Results in brief
“DNA-based NANOdevices for the point-of-care electrochemical detection of AntiBodies”
The present fellowship proposes the development and characterization of electrochemical platforms to monitor the quantitative detection of clinically-relevant antibodies, that will be rapid, specific, convenient and selective enough to be employed directly in complex samples, such as blood serum and whole blood. The detection of specific antibodies and other diagnostic proteins plays a crucial role in the diagnosis of many diseases, infections and pathologies and despite their widespread use current detection methods are either cumbersome, multi-step and laboratory-bound processes (i.e., ELISA, western blot) or only qualitative or semi-quantitative (i.e., later flow immunoassay). Due to the above considerations, better analytical tools that allow the rapid, inexpensive, and quantitative measurement of clinically-relevant biomarkers, including antibodies, are urgently needed. To address this need, during my Marie-Skłodowska Curie project (“DNA-NANO-AB”), I have developed different DNA-based sensors and devices for the detection of a wide range of molecules, including antibodies, that may be of utility for diagnostic applications. To do so, I employ the designability and versatility of synthetic DNA sequences those can be used as scaffolds to create antibody-responsive nanodevices and I take advantage of the positive feature of electrochemical detection that include interference-free measurements in complex matrices, low-cost instrumentation and mass-producible sensors. To reach the proposed objectives I will undertake the following tasks: 1. Rational design and characterization of different DNA-based strategies (conformational change, proximity-based approach, etc.) to improve target measurement efficiency using spectroscopic and electrochemical-based approaches. Different DNA-based elements will be tested as well as several recognition element/antibody couples. 2. Development and optimization of versatile electrochemical platforms for the orthogonal and multiplexed antibodies detection. Systematic study of: i) redox reporters, ii) antigen tags, iii) electrochemical parameters, iv) signal amplification. 3. Development of platforms using disposable screen-printed electrodes produced in house to reduce the fabrication cost of each sensor. 4. Test of representative real samples using the developed electrochemical platform. The platforms will be firstly challenged with blood serum and ultimately with whole blood. In conclusion “DNA-NANO-AB” has paved the basis for new classes of DNA-based sensors for antibody detection. Specifically, the possibility of coupling the advantages of synthetic nucleic acids with the positive feature of electrochemical detection and the possible amplification processes to enhance the sensibility of the sensors make the sensing platforms developed during this project well suited for point-of-care applications.
Data: CORDIS, © European Union
Project objective
WHY: Antibody detection plays a pivotal role in the diagnosis of many human disorders including infectious, autoimmune, and oncological diseases. Unfortunately, current methods routinely used for the detection of these biomarkers still require sophisticated equipment, washing intensive, reagent-intensive multi-step processes. In attempt to overcome the cited limitations, it’s mandatory find new approaches for the sensitive detection of antibodies. WHAT: DNA-NANO-AB proposes the development of DNA-based novel, rapid, user friendly, robust, sensitive and low cost electrochemical NANOdevices for orthogonal multiplex detection of antibodies that may be advantageous over existing methods for the detection of clinically-relevant antibodies and could be well-positioned for point-of-care applications. I will achieve this goal by rationally designing and fabricating disposable DNA-based sensing platforms in which the detection of specific antibodies will be signaled, and amplified, through an electrochemical read-out approach. The developed platforms will be characterized, optimized and then tested for the dosage of immunoglobulins levels directly in real representative samples. HOW: During the fellowship I will undertake a training program to develop skills and acquire expertise in molecular biology, electrochemical biosensor and DNA Nanotechnology. To achieve these objectives, I will combine the different scientific backgrounds and expertise of two leading scientists: Prof. Plaxco (University of California Santa Barbara), a world-wide expert in electrochemical biosensors, and Prof. Ricci (University of Rome, Tor Vergata), a young researcher active at the forefront of DNA nanotechnology for diagnostic and drug-delivery applications. Thanks to this MSC Fellowship, I will diversify my scientific knowledge and acquire cutting-edge competences as well as complementary skills, which will become the foundation of my scientific independence.
Original text from CORDIS.
Participants
- UNIVERSITA DEGLI STUDI DI ROMA TOR VERGATA · RomaCoordinatorItaly
- THE REGENTS OF THE UNIVERSITY OF CALIFORNIA · OaklandUnited States
Links
Data: CORDIS, © European Union
