Results 61 to 70 of about 3,934,989 (303)

Three dimensional protein assemblies directed by orthogonal non covalent interactions [PDF]

open access: yes, 2016
In this report, an orthogonal non covalent interaction strategy based on specific recognition between sugar and protein, and host guest interaction, was employed to construct artificial three dimensional 3D protein assemblies in the ...
Yang, Guang.   +6 more
core   +1 more source

Dataset for "Large 31P-NMR enhancements in liquid state dynamic nuclear polarization through radical/target molecule non-covalent interaction"

open access: yes, 2023
We provide raw data associated with the manuscript "Large 31P-NMR enhancements in liquid state dynamic nuclear polarization through radical/target molecule non-covalent interaction", DOI: https://doi.org/10.1039/d2cp04092a. A description of the uploaded
Levien, Marcel   +3 more
core   +1 more source

Going viral − Virus‐targeting nanobodies for research, diagnostics and therapy

open access: yesFEBS Letters, EarlyView.
The increasing prevalence of viral diseases represents a major threat for global human health. Nanobodies, small binding fragments derived from camelid heavy‐chain antibodies, offer versatile tools for viral research, diagnostics, and antiviral therapy.
Domenic Ebert, Ulrich Rothbauer
wiley   +1 more source

Metal-Based Drug–DNA Interactions and Analytical Determination Methods

open access: yesMolecules
DNA structure has many potential places where endogenous compounds and xenobiotics can bind. Therefore, xenobiotics bind along the sites of the nucleic acid with the aim of changing its structure, its genetic message, and, implicitly, its functions ...
Adriana Corina Hangan   +5 more
doaj   +1 more source

Strategic Design of Catalytic Lysine-Targeting Reversible Covalent BCR-ABL Inhibitors [PDF]

open access: yes, 2021
Targeted covalent inhibitors have re-emerged as validated drugs to overcome acquired resistance in cancer treatment. Herein, by using a carbonyl boronic acid warhead, we report the structure-based design of BCR-ABL inhibitors via reversible covalent ...
Guanghui, Tang   +16 more
core   +2 more sources

Inhibition of cyclin‐dependent kinases 12/13 using CT7439 as a treatment for colorectal cancer with CDK12 upregulation

open access: yesMolecular Oncology, EarlyView.
The proposed mechanism of action for the CDK12/13 inhibitor and cyclin K degrader, CT7439. CDK12/13 inhibition interrupts transcription elongation, leading to increased DNA damage that results in cell death. This agent is a potentially novel treatment option for patients with colorectal cancer. Created in BioRender. Cyclin‐dependent kinase (CDK) 12 and
Wylie K. Watlington   +10 more
wiley   +1 more source

The mechanism of pectin in improving anthocyanin stability and the application progress of their complexes: A review

open access: yesFood Chemistry: X
Improving anthocyanin stability is a major challenge for the food industry. Studies have revealed that the interaction with pectin through non-covalent bonds can improve the anthocyanin stability, thus showing the potential to alleviate the above ...
Chenyang Shi   +7 more
doaj   +1 more source

The effect of non-covalent functionalization on the interaction energy of carbon nanotubes

open access: yes, 2019
The Lennard-Jones potential function together with the continuous approximation is employed to determine the van der Waals interaction between two parallel cylindrical nanotubes. Here we determine the interaction energy between carbon nanotubes and those
Ruengrot, P.   +3 more
core   +1 more source

A role for eIF5A in translational control of stress‐inducible proteins in multiple myeloma cell lines

open access: yesMolecular Oncology, EarlyView.
Loss of eIF5A rewires thapsigargin‐mediated endoplasmic reticulum stress responses in multiple myeloma cells by selective translation of mRNA transcripts, consequently dampening thapsigargin‐induced unfolded protein response (UPR) activation and shifting the balance from induction of apoptosis toward cell survival and proliferation.
Demi Both   +7 more
wiley   +1 more source

Molecular Recognition of SARS-CoV-2 Mpro Inhibitors: Insights from Cheminformatics and Quantum Chemistry

open access: yesMolecules
The SARS-CoV-2 main protease (Mpro), essential for viral replication, remains a prime target for antiviral drug design against COVID-19 and related coronaviruses.
Adedapo Olosunde, Xiche Hu
doaj   +1 more source

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