Unamplified and Label‐Free Detection of HPV16 DNA Using CRISPR‐Cas12a‐Functionalized Solution‐Gated Graphene Transistors

Author:

Zhang Huibin1,Deng Minghua1,Li Ziqin1,Ren Zhanpeng1,Zhang Lei1,Wang Ming2,Jiang Shupeng2,Yu Li1,Wang Xianbao1,Li Jinhua1ORCID

Affiliation:

1. Collaborative Innovation Center for Advanced Organic Chemical Materials Co‐constructed by the Province and Ministry Key Laboratory for the Green Preparation and Application of Functional Materials Ministry of Education Hubei Key Laboratory of Polymer Materials School of Materials Science and Engineering Hubei University Wuhan 430062 China

2. Department of Clinical Laboratory Renmin Hospital of Wuhan University Wuhan 430060 China

Abstract

AbstractThe persistent infection of high‐risk‐human papillomavirus type 16 (HPV16) is considered an essential element for suffering cervical cancer. Despite polymerase chain reaction, loop‐mediated amplification, and microfluidic chips are used to detect the HPV16, these methods still exist some drawbacks including time‐consuming and false positive results. The CRISPR‐Cas system is widely used in the region of biological detection due to its precise targeted recognition capability. In this contribution, the novel solution‐gated graphene transistor sensor is designed to realize the unamplified and label‐free detection of HPV16 DNA. Using the precise recognition of the CRISPR‐Cas12a system and the gate functionalization, HPV16 DNA can be precisely identified without need the amplification and labeling. The limit of detection of the sensor can be up to 8.3 × 10−18 m and the detection can be within 20 min. Additionally, the heat‐Inactivated clinical samples can be clearly distinguished by the sensor the diagnosis results have a high degree of agreement with q‐PCR detection.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Pharmaceutical Science,Biomedical Engineering,Biomaterials

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