Results 1 to 10 of about 66,620 (264)

Gαs slow conformational transition upon GTP binding and a novel Gαs regulator

open access: yesiScience, 2023
Summary: G proteins are major signaling partners for G protein-coupled receptors (GPCRs). Although stepwise structural changes during GPCR–G protein complex formation and guanosine diphosphate (GDP) release have been reported, no information is available
Donghoon Ahn   +12 more
doaj   +1 more source

In honor of Hartmut Karl Lichtenthaler

open access: yesPhotosynthetica, 2021
We honor here Hartmut Karl Lichtenthaler, a pioneer of plant physiology, plant biochemistry, plant biophysics, plant molecular biology, and stress physiology.
G. GOVINDJEE
doaj   +1 more source

Using fluorescence anisotropy to monitor chaperone dispersal of RNA-binding protein condensates

open access: yesSTAR Protocols, 2022
Summary: Heat stress triggers a specific set of proteins in budding yeast to form solid-like biomolecular condensates, which are dispersed by molecular chaperones.
Haneul Yoo, D. Allan Drummond
doaj   +1 more source

Preparation of site-specifically fluorophore-labeled polyubiquitin chains for FRET studies of Cdc48 substrate processing

open access: yesSTAR Protocols, 2023
Summary: A critical step in the removal of polyubiquitinated proteins from macromolecular complexes and membranes for subsequent proteasomal degradation is the unfolding of an ubiquitin moiety by the cofactor Ufd1/Npl4 (UN) and its insertion into the ...
Cameron Williams   +3 more
doaj   +1 more source

Site-directed fluorescence approaches to monitor the structural dynamics of proteins using intrinsic Trp and labeled with extrinsic fluorophores

open access: yesSTAR Protocols, 2022
Summary: Comprehensive understanding of a protein’s function depends on having reliable, sophisticated tools to study protein structural dynamics in physiologically-relevant conditions.
Rupasree Brahma   +2 more
doaj   +1 more source

CRISPR/Cas12a-mediated labeling of MET receptor enables quantitative single-molecule imaging of endogenous protein organization and dynamics

open access: yesiScience, 2021
Summary: Single-molecule localization microscopy (SMLM) reports on protein organization in cells with near-molecular resolution and in combination with stoichiometric labeling enables protein counting.
Tim N. Baldering   +8 more
doaj   +1 more source

Activation of a diluted E. coli cell-free transcription-translation system within liposomes by hypertonic concentration

open access: yesSTAR Protocols, 2021
Summary: We present a protocol for activating protein synthesis in liposomes encapsulating a diluted E. coli cell extract-based TX-TL (transcription-translation) system by hypertonic concentration.
Yukino Matsui   +3 more
doaj   +1 more source

Biophysical and flavonoid-binding studies of the G protein ectodomain of group A human respiratory syncytial virus

open access: yesHeliyon, 2019
The human Respiratory Syncytial Virus (hRSV) is the major causative agent of lower respiratory tract diseases in infants, young children and elderly. The membrane protein G is embedded in the viral lipid envelope and plays an adhesion function of the ...
Vitor Brassolatti Machado   +7 more
doaj   +1 more source

Watson-Crick Base-Pairing Requirements for ssDNA Recognition and Processing in Replication-Initiating HUH Endonucleases

open access: yesmBio, 2023
Replication-initiating HUH endonucleases (Reps) are sequence-specific nucleases that cleave and rejoin single-stranded DNA (ssDNA) during rolling-circle replication.
Adam T. Smiley   +7 more
doaj   +1 more source

Fluorescence lifetime FRET assay for live-cell high-throughput screening of the cardiac SERCA pump yields multiple classes of small-molecule allosteric modulators

open access: yesScientific Reports, 2023
We have used FRET-based biosensors in live cells, in a robust high-throughput screening (HTS) platform, to identify small-molecules that alter the structure and activity of the cardiac sarco/endoplasmic reticulum calcium ATPase (SERCA2a). Our primary aim
Osha Roopnarine   +8 more
doaj   +1 more source

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