H2020Индивидуална стипендия2020–2022

GlucOrigami · Modular DNA Origami Platform for the Design of Tunable Glucose Biosensor

„Хоризонт 2020“ — Действия „Мария Склодовска-Кюри“

Период
2020-09-01 → 2022-08-31
Финансиране от ЕС
162 806 €
Участници
1
Схема
MSCA-IF

Линиите свързват координатора с партньорите.

Накратко на български

ДНК оригами се използва за създаване на модулни биосензори, които могат да засичат нива на глюкоза. Тези устройства помагат за разработването на евтини и бързи диагностични тестове, подходящи за използване с мобилни телефони в различни региони на света.

Този кратък обзор е генериран от изкуствен интелект

Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.

Резултати накратко

Modular DNA Origami Platform for the Design of Tunable Glucose Biosensor

From health monitoring to the detection of diseases, biosensors play a crucial role in our everyday lives. Unfortunately, in many cases, the practical use of biosensors requires costly instruments, time-consuming multi-step procedures and highly trained personnel to implement. Recent years, however, have witnessed tremendous efforts in the development of cheap and miniaturized optical sensing devices that can even be integrated with ubiquitous smartphone sensors and software. These point-of-care sensing approaches could not only facilitate the goal of ‘personalized medicine’ but also bring the diagnostic technology to resource-poor regions of the world where many infectious diseases are so prevalent. This technological boost creates an ever-growing need for new and improved optical biosensors capable of continuous monitoring of analytes in a single-step process with low-cost sensor devices. The development of such biosensors, nonetheless, faces several common challenges. A typical biosensor comprises a molecular recognition unit (e.g. protein or nucleic acid) and a detection unit designed to report this binding event in the form of an optical signal (e.g. as color or fluorescence change). One of the challenges here is to detect rather “inert” analytes that are not able to generate a strong optical signal upon binding to a molecular recognition site. Another challenge is posed by the strength of this molecular recognition interaction, which dictates the useful dynamic range of the biosensor. The ability to extend, narrow and tune this useful dynamic range, could greatly benefit applications where target concentrations span several orders of magnitude (e.g. monitoring progression of viral infections) or where a sharp dose response is essential to achieve high precision (e.g. monitoring of highly toxic substances). The aim of this project was to globally address these challenges by decoupling the molecular recognition and signal transduction units of the biosensor with the help of self-assembled and programmable DNA origami nanostructures. A more specific objective was to demonstrate this fundamental approach by designing a sensitive and tunable biosensor for glucose, whose sensing is of utmost importance for the disease monitoring of diabetic patients. Different biomimicry approaches were proposed to be tested that could lead to strategies to tune the useful dynamic range of the proposed biosensor platform with the aim to achieve sensitivity at a physiologically relevant glucose concentration.

Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз

Цел на проекта

Biosensors play a crucial role in our everyday lives from health monitoring to disease detection. The rapid advancement of sensing technologies dictates an ever growing need for improved biosensors which are capable to continuously monitor analytes in a single-step process and yield low-cost devices. The performance of many biosensors is, however, limited by the binding strength of their molecular recognition unit which dictates the dynamic range of the sensor and is often tightly connected to the signal transduction unit, i.e. its signal output. In this project, I propose to globally solve this limitation by decoupling the molecular recognition and signal transduction units of the biosensor by exploiting self-assembled and programmable DNA origami nanostructures. This fundamental approach will be demonstrated by the design of a sensitive and tunable biosensor for glucose, whose sensing is of utmost importance for the disease monitoring of diabetic patients. DNA origami will be utilized to precisely position all biosensor elements: multifluorophore FRET pair, which will serve as a signal transduction and amplification unit as well as glucose/galactose binding proteins and glucose functionalities, which will provide a molecular recognition unit. Different biomimicry strategies to tune the useful dynamic range of the biosensors will be evaluated aiming to achieve sensitivity at a physiologically relevant glucose concentration. Finally, the potential to combine these advanced glucose biosensors with low-cost read-out instruments (such as smartphone cameras) will be assessed. The DNA origami glucose sensor proposed here is of great promise for the development of wearable and low-cost glucose sensing devices for diabetes monitoring, which will grow into a large demand in our society. Moreover, it will allow me to merge DNA nanotechnology, molecular biology, spectroscopy and chemistry research, laying the foundations upon which to build my future career in Europe.

Оригинален текст от CORDIS (на английски).

Участници

  • LUDWIG-MAXIMILIANS-UNIVERSITAET MUENCHEN · PlaneggКоординаторГермания

Връзки

Данни: CORDIS, © Европейски съюз