controlled assembly
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2022 ◽  
Vol 216 ◽  
pp. 106340
Author(s):  
Erwin A. Henry ◽  
Emmanuelle Montarges-Pelletier ◽  
Isabelle Bihannic ◽  
Céline Caillet ◽  
Jaafar Ghanbaja ◽  
...  

Author(s):  
Akhilan Elangovan ◽  
Dhananjay Suresh ◽  
Andrew O. Tarim ◽  
Anandhi Upendran ◽  
Raghuraman Kannan

2021 ◽  
Author(s):  
Olga Firstova ◽  
Vangelis Agouridas ◽  
Vincent Diemer ◽  
Oleg Melnyk

We provide in this protocol detailed procedures for the synthesis of SetCys cysteine surrogate and its use for chemical synthesis of proteins through the redox-controlled assembly of three peptide segments in one-pot.


2021 ◽  
pp. 2103945
Author(s):  
Baipeng Yin ◽  
Wubin Wu ◽  
Chenghu Dai ◽  
Hao Jia ◽  
Chuang Zhang ◽  
...  

2021 ◽  
Vol 594 ◽  
pp. 727-736
Author(s):  
Xuejiao Wang ◽  
Xuedong Gao ◽  
Xiao Xiao ◽  
Shasha Jiang ◽  
Yun Yan ◽  
...  

Biomolecules ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 955
Author(s):  
Mark Freeley ◽  
Rebecca E. A. Gwyther ◽  
D. Dafydd Jones ◽  
Matteo Palma

Here, we report the controlled assembly of SWCNT–GFP hybrids employing DNA as a linker. Two distinct, enriched SWCNTs chiralities, (6,5), (7,6), and an unsorted SWCNT solution, were selectively functionalized with DNA and hybridized to a complementary GFPDNA conjugate. Atomic force microscopy images confirmed that GFP attachment occurred predominantly at the terminal ends of the nanotubes, as designed. The electronic coupling of the proteins to the nanotubes was confirmed via in-solution fluorescence spectroscopy, that revealed an increase in the emission intensity of GFP when linked to the CNTs.


2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Sophie Bergmann ◽  
Magdalena Schindler ◽  
Clara Munger ◽  
Christopher A. Penfold ◽  
Thorsten E. Boroviak

AbstractThe uterus is the organ for embryo implantation and fetal development. Most current models of the uterus are centred around capturing its function during later stages of pregnancy to increase the survival in pre-term births. However, in vitro models focusing on the uterine tissue itself would allow modelling of pathologies including endometriosis and uterine cancers, and open new avenues to investigate embryo implantation and human development. Motivated by these key questions, we discuss how stem cell-based uteri may be engineered from constituent cell parts, either as advanced self-organising cultures, or by controlled assembly through microfluidic and print-based technologies.


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