Analysis of Arc/Arg3.1 Oligomerization In Vitro and in Living Cells

• Published in: International journal of molecular sciences Vol. 25; no. 12; p. 6454
• Main Authors: Barylko, Barbara, Taylor, 4th, Clinton A, Wang, Jason, Hedde, Per Niklas, Chen, Yan, Hur, Kwang-Ho, Binns, Derk D, Brautigam, Chad A, DeMartino, George N, Mueller, Joachim D, Jameson, David M, Albanesi, Joseph P
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01-06-2024; MDPI
• Subjects: activity-regulated-cytoskeleton-associated protein; Animals; Arc/Arg3.1; Communication; Cytoskeletal Proteins - chemistry; Cytoskeletal Proteins - genetics; Cytoskeletal Proteins - metabolism; Fluorescence; fluorescence fluctuation spectroscopy; fluorescence lifetime imaging; Förster resonance energy transfer; Humans; Kinases; Muscle proteins; Nerve Tissue Proteins - chemistry; Nerve Tissue Proteins - genetics; Nerve Tissue Proteins - metabolism; oligomerization; Oligomers; Phosphorylation; Protein Multimerization; Proteins; RNA; Spectrum analysis; Massachusetts; Förster resonance energy transfer; activity-regulated-cytoskeleton-associated protein; fluorescence lifetime imaging; Arc/Arg3.1; oligomerization; fluorescence fluctuation spectroscopy
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms25126454

Arc (also known as Arg3.1) is an activity-dependent immediate early gene product enriched in neuronal dendrites. Arc plays essential roles in long-term potentiation, long-term depression, and synaptic scaling. Although its mechanisms of action in these forms of synaptic plasticity are not completely well established, the activities of Arc include the remodeling of the actin cytoskeleton, the facilitation of AMPA receptor (AMPAR) endocytosis, and the regulation of the transcription of AMPAR subunits. In addition, Arc has sequence and structural similarity to retroviral Gag proteins and self-associates into virus-like particles that encapsulate mRNA and perhaps other cargo for intercellular transport. Each of these activities is likely to be influenced by Arc's reversible self-association into multiple oligomeric species. Here, we used mass photometry to show that Arc exists predominantly as monomers, dimers, and trimers at approximately 20 nM concentration in vitro. Fluorescence fluctuation spectroscopy revealed that Arc is almost exclusively present as low-order (monomer to tetramer) oligomers in the cytoplasm of living cells, over a 200 nM to 5 μM concentration range. We also confirmed that an α-helical segment in the N-terminal domain contains essential determinants of Arc's self-association.