Biochemical Interaction and Supramolecular Complexes of Receptors in Cell Membranes

A special issue of Cells (ISSN 2073-4409).

Deadline for manuscript submissions: 8 July 2026 | Viewed by 1508

Special Issue Editors


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Guest Editor
Department of Molecular and Translational Medicine, University of Brescia, 25123 Brescia, Italy
Interests: angiogenesis; ECM; imaging; animal models; tumors
Special Issues, Collections and Topics in MDPI journals

E-Mail Website
Guest Editor
Department of Molecular and Translational Medicine, University of Brescia, 25123 Brescia, Italy
Interests: angiogenesis; membrane receptor; tumors; imaging; metabolism; bioscaffold for tissue regeneration
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

The intricate interplay of biochemical interactions and supramolecular complexes formed by receptors in cell membranes constitutes a fundamental aspect of cellular metabolic regulation. Receptors detect and respond to various extracellular signals, ensuring proper cellular function and homeostasis. Ligands induce receptor activation supporting receptor–receptor and/or receptor–coreceptor interaction. Oligomerization is widely acknowledged as a fundamental mechanism for activating various types of receptors, including hormone and growth factor receptors, G protein-coupled receptors (GPCRs), lymphokine receptors, T- and B-cell receptors, and other families of cell surface receptors. In response to extracellular stimuli, receptors undergo dynamic modifications in their affinity and persist in the supramolecular complexes state. Consequently, "short-lived complexes" emerge, maintaining a dynamic equilibrium with monomers that freely diffuse within the cellular membrane.

Dysfunction or dysregulation of receptor dynamics can lead to a wide range of diseases.

In various pathological conditions, the aberrant activation of receptors or dysregulated downstream signaling pathways have been described as inducers of atypical cell behavior and cell metabolism. Disturbances in receptor-mediated signaling have been linked to cardiovascular diseases, neurodegenerative disorders, autoimmune diseases, endocrine disorders, cancers, and many other conditions.

In this Special Issue, we invite contributions that shed light on the biochemical interactions and supramolecular complexes of cell membrane receptors and the development of chemosensors and molecular probes to highlight receptor behavior. We encourage researchers to submit manuscripts presenting original research findings, innovative methodologies, and conceptual advances in this field. The aim is to deepen our understanding of the mechanisms underlying receptor-mediated signaling and explore the potential therapeutic implications.

Topics of interest include, but are not limited to, the following:

  • Ligand-induced receptor activation and oligomerization;
  • Receptor–ligand binding kinetics and thermodynamics;
  • Chemosensors for receptor activation;
  • Structural insights into receptor complexes and their functional implications;
  • Modulation of receptor biochemistry by membrane microdomains and development of molecular probes for receptors dynamics;
  • Supramolecular complexes and chemosensors for downstream signaling cascades;
  • Receptor clustering and spatial organization in the cell membrane;
  • Role of receptor oligomerization in cellular processes and disease pathogenesis;
  • Emerging RNA technologies and experimental approaches to study receptor complexes;
  • Therapeutic targeting of receptor complexes for disease intervention.

By compiling a diverse collection of research articles, reviews, and perspectives, this Special Issue aims to foster collaboration and exchange of knowledge among researchers working on the intricate biochemical interactions and supramolecular complexes of receptors in cell membranes.

We welcome researchers from various disciplines to contribute their expertise and insights to this Special Issue, providing a comprehensive overview of the current understanding and future directions in the field of receptor biology and cell membrane signaling.

Dr. Michela Corsini
Prof. Dr. Stefania Mitola
Guest Editors

Manuscript Submission Information

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Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • membrane receptors
  • molecular complex
  • membrane microdomains

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Published Papers (1 paper)

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Review

19 pages, 880 KB  
Review
Lipid–Protein Interplay in the Regulation of Receptor Tyrosine Kinases
by Mattia Domenichini, Anna Gogna, Camilla Maggi, Elisa Moreschi, Anna Ventura, Martina Codibue, Elisabetta Grillo, Michela Corsini and Stefania Mitola
Cells 2025, 14(23), 1836; https://doi.org/10.3390/cells14231836 - 21 Nov 2025
Viewed by 799
Abstract
Receptor tyrosine kinases (RTKs), a class of membrane proteins involved in several physiological processes such as growth, survival, angiogenesis, and differentiation, are profoundly influenced by the microenvironment, particularly by surrounding lipids. Lipids coordinate RTK life cycle at multiple steps. First, receptor lipidation is [...] Read more.
Receptor tyrosine kinases (RTKs), a class of membrane proteins involved in several physiological processes such as growth, survival, angiogenesis, and differentiation, are profoundly influenced by the microenvironment, particularly by surrounding lipids. Lipids coordinate RTK life cycle at multiple steps. First, receptor lipidation is a key post-translational modification for receptor-targeting localization. Then, RTK dimerization and activation are regulated by membrane-enriched lipids like phosphatidylserine and phosphoinositides, gangliosides, and Cholesterol, which directly engage RTK juxtamembrane domain or cytoplasmic tail. Eventually, lipids spatially organize RTK signaling within Cholesterol- and sphingolipid-enriched membrane microdomains. These membrane rafts act as dynamic “signalosomes” coordinating receptor clustering, endocytosis, and recycling. Perturbations in lipid composition remodel raft architecture and alter RTK behavior, contributing to pathological conditions such as cancer, metabolic, and neurodegenerative disorders. Emerging lipid-targeted therapies offer a promising way to enhance RTK-directed therapies. This review aims to explore how specific lipid species and membrane domains modulate RTK activation, clustering, and endocytic recycling. By bridging biochemical and pathological perspectives, we discuss how membrane lipid composition reshapes RTK signaling in physiology and pathology, pointing to emerging opportunities for lipid-focused therapeutic modulation. Full article
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