Faculty Opinions recommendation of Genetically encoded multivalent liquid glycan array displayed on M13 bacteriophage.

Author(s):  
Jeff Gildersleeve
RSC Advances ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 1367-1375
Author(s):  
Jing Yi Lai ◽  
Naoya Inoue ◽  
Chuan Wei Oo ◽  
Hideya Kawasaki ◽  
Theam Soon Lim

M13 bacteriophage is an attractive alternative source for fluorescent nanoparticle synthesis.


Gene ◽  
1993 ◽  
Vol 128 (1) ◽  
pp. 29-36 ◽  
Author(s):  
M.A. McLafferty ◽  
R.B. Kent ◽  
R.C. Ladner ◽  
W. Markland
Keyword(s):  

Sensors ◽  
2021 ◽  
Vol 21 (3) ◽  
pp. 986
Author(s):  
Daun Seol ◽  
Daeil Jang ◽  
Kyungjoon Cha ◽  
Jin-Woo Oh ◽  
Hoeil Chung

A single M13 bacteriophage color sensor was previously utilized for discriminating the geographical origins of agricultural products (garlic, onion, and perilla). The resulting discrimination accuracy was acceptable, ranging from 88.6% to 94.0%. To improve the accuracy further, the use of three separate M13 bacteriophage color sensors containing different amino acid residues providing unique individual color changes (Wild sensor: glutamic acid (E)-glycine (G)-aspartic acid (D), WHW sensor: tryptophan (W)-histidine (H)-tryptophan (W), 4E sensor: four repeating glutamic acids (E)) was proposed. This study was driven by the possibility of enhancing sample discrimination by combining mutually characteristic and complimentary RGB signals obtained from each color sensor, which resulted from dissimilar interactions of sample odors with the employed color sensors. When each color sensor was used individually, the discrimination accuracy based on support vector machine (SVM) ranged from 91.8–94.0%, 88.6–90.3%, and 89.8–92.1% for garlic, onion, and perilla samples, respectively. Accuracy improved to 98.0%, 97.5%, and 97.1%, respectively, by integrating all of the RGB signals acquired from the three color sensors. Therefore, the proposed strategy was effective for improving sample discriminability. To further examine the dissimilar responses of each color sensor to odor molecules, typical odor components in the samples (allyl disulfide, allyl methyl disulfide, and perillaldehyde) were measured using each color sensor, and differences in RGB signals were analyzed.


2021 ◽  
pp. 113693
Author(s):  
Jong-Min Lee ◽  
Vasanthan Devaraj ◽  
Na-Na Jeong ◽  
Yujin Lee ◽  
Ye-Ji Kim ◽  
...  

2015 ◽  
Vol 12 (3) ◽  
pp. 271-281 ◽  
Author(s):  
Jong-Sik Moon ◽  
Won-Geun Kim ◽  
Chuntae Kim ◽  
Geun-Tae Park ◽  
Jeong Heo ◽  
...  

2013 ◽  
Vol 24 (14) ◽  
pp. 2079-2084 ◽  
Author(s):  
Ju Hun Lee ◽  
Phyllis F. Xu ◽  
Dylan W. Domaille ◽  
Chulmin Choi ◽  
Sungho Jin ◽  
...  

Toxins ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 781
Author(s):  
Zhuolin Song ◽  
Lin Feng ◽  
Yuankui Leng ◽  
Mingzhu Huang ◽  
Hao Fang ◽  
...  

Enzyme-linked immunosorbent assay (ELISA) is widely used in the routine screening of mycotoxin contamination in various agricultural and food products. Herein, a cascade-amplifying system was introduced to dramatically promote the sensitivity of an immunoassay for ochratoxin A (OTA) detection. Specifically, a biotinylated M13 bacteriophage was introduced as a biofunctional competing antigen, in which a seven-peptide OTA mimotope fused on the p3 protein of M13 was used to specifically recognize an anti-OTA monoclonal antibody, and the biotin molecules modified on capsid p8 proteins were used in loading numerous streptavidin-labeled polymeric horseradish peroxidases (HRPs). Owing to the abundance of biotinylated p8 proteins in M13 and the high molar ratio between HRP and streptavidin in streptavidin-polyHRP, the loading amount of HRP enzymes on the M13 bacteriophage were greatly boosted. Hence, the proposed method exhibited high sensitivity, with a limit of detection of 2.0 pg/mL for OTA detection, which was 250-fold lower than that of conventional ELISA. In addition, the proposed method showed a slight cross-reaction of 2.3% to OTB, a negligible cross-reaction for other common mycotoxins, and an acceptable accuracy for OTA quantitative detection in real corn samples. The practicability of the method was further confirmed with a traditional HRP-based ELISA method. In conclusion, the biotinylated bacteriophage and polyHRP structure showed potential as a cascade-amplifying enzyme loading system for ultra-trace OTA detemination, and its application can be extended to the detection of other analytes by altering specific mimic peptide sequences.


2017 ◽  
Vol 58 ◽  
pp. 527-538 ◽  
Author(s):  
Yuhua Sun ◽  
Yiting Li ◽  
Baohua Wu ◽  
Jianxin Wang ◽  
Xiong Lu ◽  
...  

2019 ◽  
Vol 17 (23) ◽  
pp. 5666-5670 ◽  
Author(s):  
Won-Geun Kim ◽  
Chris Zueger ◽  
Chuntae Kim ◽  
Winnie Wong ◽  
Vasanthan Devaraj ◽  
...  

This study includes the experimental results of a sensitive M13 bacteriophage-based sensor system that are well matched with the quantum mechanics calculation.


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