噬菌体
噬菌体展示
纳米技术
滚动圆复制
计算生物学
适体
材料科学
生物物理学
化学
基因
肽
分子生物学
生物
遗传学
生物化学
聚合酶
大肠杆菌
作者
Ying Cao,Na Wu,Hui‐Da Li,Jing‐Wen Xue,Rui Wang,Ting Yang,Jianhua Wang
出处
期刊:Small
[Wiley]
日期:2022-11-03
卷期号:18 (51)
被引量:5
标识
DOI:10.1002/smll.202203962
摘要
Abstract The M13 bacteriophage (M13 phage) has emerged as an attractive bionanomaterial due to its chemistry/gene modifiable feature and unique structures. Herein, a dynamic deformable nanointerface is fabricated taking advantage of the unique feature of the M13 phage for ultrasensitive detection of pathogens. PIII proteins at the tip of the M13 phage are genetically modified to display 6His peptide for site‐specific anchoring onto Ni‐NTA microbeads, whereas pVIII proteins along the side of the M13 phage are orderly arranged with thousands of aptamers and their complementary strands (c‐apt). The flexible M13 nanofibers with rich recognition sites act as octopus tentacles, resulting in a 19‐fold improvement in the capture affinity toward the target. The competitive binding of the target pathogen releases c‐apts and initiates rolling circle amplification (RCA). The sway motion of M13 nanofibers accelerates the diffusion of c‐apts, thus promoting RCA efficiency. Benefiting from the strengthened capture ability toward the target and the accelerated RCA process, three‐orders of magnitude improvement in the sensitivity is achieved, with a detection limit of 8 cfu mL −1 for Staphylococcus aureus . The promoted capture ability and assay performance highlights the essential role of the deformable feature of the engineered interface. This may provide inspiration for the construction of more efficient reaction interfaces.
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