Application of Functional Nucleic Acid Based Biosensors in Cell or Tissue Analysis

A special issue of Biosensors (ISSN 2079-6374). This special issue belongs to the section "Biosensors and Healthcare".

Deadline for manuscript submissions: 31 October 2024 | Viewed by 1090

Special Issue Editor


E-Mail Website
Guest Editor
Faculty of Materials Science and Chemistry, China University of Geosciences, Wuhan, China
Interests: single cell analysis DNA nanotechnology

Special Issue Information

Dear Colleagues,

Functional nucleic acids, such as aptamers and DNAzymes, have excellent flexibility, are convenient in their structural design, and thus possess significant advantages as recognition elements (probes) in biosensing. Combining functional nucleic acids with signal amplification methods offers a promising technique by which to achieve signal-amplified target detection. Functional DNA nanostructures are easily constructed and highly programmable, such that shapes and their sizes can be designed. Compared to small molecules, functional nucleic acid structures are more efficiently endocytosed by cells. For example, the structure of a tetrahedron can be transferred to the cell without transfection. In addition, sensitive and accurate diagnosis and treatment can be achieved by integrating various units into functional nucleic acid probes, such as imaging agents, aptamers for cancer targets, and cancer therapeutic drugs. In recent decades, various biosensing strategies based on functional nucleic acids and functional DNA nanostructures with amplified signals have been developed to achieve signal-amplified cell imaging and tissue analysis. The labeling of DNA nanostructures with fluorescent dyes is one of the techniques most often employed to track the spatial location of biomarkers inside cells. Many in situ amplifications have been developed for cell imaging and tissue analysis via FRET signals. Encouraged by the developments concerning functional nucleic acids in cell imaging and tissues analysis, greater valuable information of the cell or tissue should be provided.

Prof. Dr. Fujian Huang
Guest Editor

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Biosensors is an international peer-reviewed open access monthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • functional nucleic acids probe
  • aptamer
  • DNAzyme
  • DNA nanostructure
  • signal amplification
  • biosensing
  • cell imaging
  • tissue analysis
  • fluorescence signal

Published Papers (1 paper)

Order results
Result details
Select all
Export citation of selected articles as:

Research

13 pages, 6824 KiB  
Article
Ultrasensitive 3D Stacked Silicon Nanosheet Field-Effect Transistor Biosensor with Overcoming Debye Shielding Effect for Detection of DNA
by Yinglu Li, Shuhua Wei, Enyi Xiong, Jiawei Hu, Xufang Zhang, Yanrong Wang, Jing Zhang, Jiang Yan, Zhaohao Zhang, Huaxiang Yin and Qingzhu Zhang
Biosensors 2024, 14(3), 144; https://doi.org/10.3390/bios14030144 - 14 Mar 2024
Viewed by 857
Abstract
Silicon nanowire field effect (SiNW-FET) biosensors have been successfully used in the detection of nucleic acids, proteins and other molecules owing to their advantages of ultra-high sensitivity, high specificity, and label-free and immediate response. However, the presence of the Debye shielding effect in [...] Read more.
Silicon nanowire field effect (SiNW-FET) biosensors have been successfully used in the detection of nucleic acids, proteins and other molecules owing to their advantages of ultra-high sensitivity, high specificity, and label-free and immediate response. However, the presence of the Debye shielding effect in semiconductor devices severely reduces their detection sensitivity. In this paper, a three-dimensional stacked silicon nanosheet FET (3D-SiNS-FET) biosensor was studied for the high-sensitivity detection of nucleic acids. Based on the mainstream Gate-All-Around (GAA) fenestration process, a three-dimensional stacked structure with an 8 nm cavity spacing was designed and prepared, allowing modification of probe molecules within the stacked cavities. Furthermore, the advantage of the three-dimensional space can realize the upper and lower complementary detection, which can overcome the Debye shielding effect and realize high-sensitivity Point of Care Testing (POCT) at high ionic strength. The experimental results show that the minimum detection limit for 12-base DNA (4 nM) at 1 × PBS is less than 10 zM, and at a high concentration of 1 µM DNA, the sensitivity of the 3D-SiNS-FET is approximately 10 times higher than that of the planar devices. This indicates that our device provides distinct advantages for detection, showing promise for future biosensor applications in clinical settings. Full article
Show Figures

Figure 1

Back to TopTop