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Photolabeling of brain membrane proteins by lysergic acid diethylamide

Anne C. Mahon, Paul R. Hartig

Life Sciences April 5, 1982 DOI: 10.1016/0024-3205(82)90660-9 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Laboratory experiment Peer reviewed
Population Bovine caudate membranes
Intervention ultraviolet light illumination
Topics LSD
Citations 7
Key findings Photolabeling of bovine caudate membranes with 3H-LSD is not specific for LSD binding sites associated with neurotransmitter receptors and can occur under room lighting, potentially introducing artifacts into receptor binding assays.

Abstract

3H-Lysergic acid diethylamide (3H-LSD) is irreversibly incorporated into bovine caudate membranes during ultraviolet light illumination. The incorporated radioligand apparently forms a covalent bond with a subpopulation of the membrane proteins. Although the photolabeling pattern differs significantly from the Coomassie blue staining pattern on SDS gels, the photolabeling is apparently not specific for LSD binding sites associated with neurotransmitter receptors. 3H-LSD photolabeling can occur during prolonged exposure of membrane samples to room lighting and thus may introduce artifacts into receptor binding assays.

Comparable studies

Other experimental studies on LSD, most cited first.

Study Year Design Participants
Neural correlates of the LSD experience revealed by multimodal neuroimaging. Human participants 2016 Experimental study
Crystal structure of an LSD-bound human serotonin receptor 2017 Experimental study with structural biology and molecular dynamics simulations
Lysergic Acid Diethylamide: Sensitive Neuronal Units in the Midbrain Raphe Midbrain neurons containing serotonin 1968 Experimental study
Connectome-harmonic decomposition of human brain activity reveals dynamical repertoire re-organization under LSD. Human brain 2017 Experimental study
LSD-Assisted Psychotherapy in Patients with Terminal Cancer Cancer patients 1973 Experimental study n = 60

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