scholarly journals Discovery of (meth)acrylate polymers that resist colonization by fungi associated with pathogenesis and biodeterioration

2020 ◽  
Vol 6 (23) ◽  
pp. eaba6574 ◽  
Author(s):  
Cindy Vallieres ◽  
Andrew L. Hook ◽  
Yinfeng He ◽  
Valentina Cuzzucoli Crucitti ◽  
Grazziela Figueredo ◽  
...  

Fungi have major, negative socioeconomic impacts, but control with bioactive agents is increasingly restricted, while resistance is growing. Here, we describe an alternative fungal control strategy via materials operating passively (i.e., no killing effect). We screened hundreds of (meth)acrylate polymers in high throughput, identifying several that reduce attachment of the human pathogen Candida albicans, the crop pathogen Botrytis cinerea, and other fungi. Specific polymer functional groups were associated with weak attachment. Low fungal colonization materials were not toxic, supporting their passive, anti-attachment utility. We developed a candidate monomer formulation for inkjet-based 3D printing. Printed voice prosthesis components showed up to 100% reduction in C. albicans biofilm versus commercial materials. Furthermore, spray-coated leaf surfaces resisted fungal infection, with no plant toxicity. This is the first high-throughput study of polymer chemistries resisting fungal attachment. These materials are ready for incorporation in products to counteract fungal deterioration of goods, food security, and health.

2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Yang Zhang ◽  
Tuan M. Nguyen ◽  
Xiao-Ou Zhang ◽  
Limei Wang ◽  
Tin Phan ◽  
...  

AbstractShort hairpin RNAs (shRNAs) are used to deplete circRNAs by targeting back-splicing junction (BSJ) sites. However, frequent discrepancies exist between shRNA-mediated circRNA knockdown and the corresponding biological effect, querying their robustness. By leveraging CRISPR/Cas13d tool and optimizing the strategy for designing single-guide RNAs against circRNA BSJ sites, we markedly enhance specificity of circRNA silencing. This specificity is validated in parallel screenings by shRNA and CRISPR/Cas13d libraries. Using a CRISPR/Cas13d screening library targeting > 2500 human hepatocellular carcinoma-related circRNAs, we subsequently identify a subset of sorafenib-resistant circRNAs. Thus, CRISPR/Cas13d represents an effective approach for high-throughput study of functional circRNAs.


Lab on a Chip ◽  
2017 ◽  
Vol 17 (19) ◽  
pp. 3264-3271 ◽  
Author(s):  
Hesam Parsa ◽  
Bryan Z. Wang ◽  
Gordana Vunjak-Novakovic

Currentin vitromodels fall short in deciphering the mechanisms of cardiac hypertrophy induced by volume overload.


2019 ◽  
Vol 108 ◽  
pp. 100-108 ◽  
Author(s):  
Yi Ouyang ◽  
Mingxiao Zhang ◽  
Jun Li ◽  
Aru Yan ◽  
Jian Liu

2020 ◽  
Vol 5 (4) ◽  
pp. 1062-1070 ◽  
Author(s):  
Yanran Li ◽  
Si Wang ◽  
Yuanjun Dong ◽  
Ping Mu ◽  
Yun Yang ◽  
...  

2020 ◽  
Vol 117 (24) ◽  
pp. 13261-13266 ◽  
Author(s):  
Alison A. Bayly ◽  
Benjamin R. McDonald ◽  
Milan Mrksich ◽  
Karl A. Scheidt

Modern organic reaction discovery and development relies on the rapid assessment of large arrays of hypothesis-driven experiments. The time-intensive nature of reaction analysis presents the greatest practical barrier for the execution of this iterative process that underpins the development of new bioactive agents. Toward addressing this critical bottleneck, we report herein a high-throughput analysis (HTA) method of reaction mixtures by photocapture on a 384-spot diazirine-terminated self-assembled monolayer, and self-assembled monolayers for matrix-assisted laser desorption/ionization mass spectrometry (SAMDI-MS) analysis. This analytical platform has been applied to the identification of a single-electron-promoted reductive coupling of acyl azolium species.


2012 ◽  
Vol 26 ◽  
pp. 98-109 ◽  
Author(s):  
Robert Zarnetta ◽  
Pio John S. Buenconsejo ◽  
Alan Savan ◽  
Sigurd Thienhaus ◽  
Alfred Ludwig

2011 ◽  
Vol 19 (10) ◽  
pp. 472-482 ◽  
Author(s):  
Jesse R.R. Zaneveld ◽  
Laura Wegener Parfrey ◽  
Will Van Treuren ◽  
Catherine Lozupone ◽  
Jose C. Clemente ◽  
...  

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