Protein bioelectronics: A review of what we do and do not know

CD Bostick, S Mukhopadhyay, I Pecht… - Reports on Progress …, 2018 - iopscience.iop.org
We review the status of protein-based molecular electronics. First, we define and discuss
fundamental concepts of electron transfer and transport in and across proteins and …

Surface plasmon resonance as a fascinating approach in target-based drug discovery and development

S Das, S Singh, V Chawla, PA Chawla… - TrAC Trends in Analytical …, 2023 - Elsevier
Abstract Surface Plasmon Resonance (SPR) technology has been proven to be a significant
approach for target-based drug discovery and development in the modern era. SPR unfolds …

De novo truncating variants in the last exon of SEMA6B cause progressive myoclonic epilepsy

K Hamanaka, E Imagawa, E Koshimizu… - The American Journal of …, 2020 - cell.com
De novo variants (DNVs) cause many genetic diseases. When DNVs are examined in the
whole coding regions of genes in next-generation sequencing analyses, pathogenic DNVs …

De Novo Biosynthesis of Caffeic Acid from Glucose by Engineered Saccharomyces cerevisiae

Y Li, J Mao, Q Liu, X Song, Y Wu, M Cai… - ACS Synthetic …, 2020 - ACS Publications
Caffeic acid is a plant phenolic compound possessing extensive pharmacological activities.
Here, we identified that p-coumaric acid 3-hydroxylase from Arabidopsis thaliana was …

Mechanism of electron transfers mediated by cytochromes c and b5 in mitochondria and endoplasmic reticulum: classical and murburn perspectives

DA Gideon, V Nirusimhan, JC E… - Journal of …, 2022 - Taylor & Francis
We explore the mechanism of electron transfers mediated by cytochrome c, a soluble protein
involved in mitochondrial oxidative phosphorylation and cytochrome b 5, a microsomal …

Time-dependent enzyme inactivation: numerical analyses of in vitro data and prediction of drug-drug interactions

J Yadav, E Paragas, K Korzekwa, S Nagar - Pharmacology & therapeutics, 2020 - Elsevier
Cytochrome P450 (CYP) enzyme kinetics often do not conform to Michaelis-Menten
assumptions, and time-dependent inactivation (TDI) of CYPs displays complexities such as …

Physical studies of P450–P450 interactions: predicting quaternary structures of P450 complexes in membranes from their X-ray crystal structures

JR Reed, WL Backes - Frontiers in pharmacology, 2017 - frontiersin.org
Cytochrome P450 enzymes, which catalyze oxygenation reactions of both exogenous and
endogenous chemicals, are membrane bound proteins that require interaction with their …

A new insight into subinteractomes of functional antagonists: Thromboxane (CYP5A1) and prostacyclin (CYP8A1) synthases

PV Ershov, E Yablokov, V Zgoda… - Cell Biology …, 2021 - Wiley Online Library
The current article aims to summarize all possible spectrum of protein–protein interactions
for thromboxane A synthase (CYP5A1) and prostacyclin synthase (CYP8A1). These …

Structural modeling of cytochrome P450 51 from a deep-sea fish points to a novel structural feature in other CYP51s

JV Goldstone, DC Lamb, SL Kelly, GI Lepesheva… - Journal of Inorganic …, 2023 - Elsevier
Abstract Cytochromes P450 (CYP), enzymes involved in the metabolism of endogenous and
xenobiotic substrates, provide an excellent model system to study how membrane proteins …

Advances in the understanding of protein-protein interactions in drug metabolizing enzymes through the use of biophysical techniques

JN Lampe - Frontiers in Pharmacology, 2017 - frontiersin.org
In recent years, a growing appreciation has developed for the importance of protein-protein
interactions to modulate the function of drug metabolizing enzymes. Accompanied with this …