The UV research groups (GIUV) are regulated in the 1st chapter of the Regulation ACGUV48/2013, which explains the procedure for creating new research structures. They are basic research and organizational structures that result from the voluntary association of researchers that share objectives, facilities, resources and common lines of research. These researchers are also committed to the consolidation and stability of their activity, work in groups and the capability to achieve a sustainable funding.
The research groups included in the previously mentioned Regulation are registered in the Register of Research Structures of the Universitat de València (REIUV), managed by the Office of the Vice-principal for Research. The basic information of these organisms can be found in this website.
Participants
Data related to research groups featured in various information dissemination channels shall not, under any circumstances, imply a statement or commitment regarding the employment or academic affiliation of individuals associated with the Universitat de València. Their inclusion is solely the responsibility of the group directors. Updates will be made upon request from interested parties.
- Registered groups in the Register of Research Structures of the Universitat de València - (REIUV)
Reference of the Group:
Description of research activity: The purposes of our projects are to explore the mechanistic principles of membrane protein insertion, folding and assembly into lipid membranes and to investigate the factors that determine membrane protein stability. Our interest focuses on protein/protein-interactions relevant for maintaining tertiary and quaternary structure and function of integral membrane protein complexes. More specifically, we investigate the role of membrane-spanning domains, i.e. of transmembrane segments. The study is performed through an exhaustive investigation of glycophorin A as a model dimeric membrane protein, and from the knowledge of this system we try to understand the structure and function of the pulmonary surfactant SP-C protein, an extremely hydrophobic membrane protein. On the other hand, we are interested in the cell-to-cell transport of plant virus. This transport process is mediated by specialized viral movement proteins, which in same cases are membrane proteins, that drive the viral genome to the cellular membrane in order to be transported into neighbouring uninfected host cells through the plasmodesmal channel. We are currently investigating the targeting and the insertion...The purposes of our projects are to explore the mechanistic principles of membrane protein insertion, folding and assembly into lipid membranes and to investigate the factors that determine membrane protein stability. Our interest focuses on protein/protein-interactions relevant for maintaining tertiary and quaternary structure and function of integral membrane protein complexes. More specifically, we investigate the role of membrane-spanning domains, i.e. of transmembrane segments. The study is performed through an exhaustive investigation of glycophorin A as a model dimeric membrane protein, and from the knowledge of this system we try to understand the structure and function of the pulmonary surfactant SP-C protein, an extremely hydrophobic membrane protein. On the other hand, we are interested in the cell-to-cell transport of plant virus. This transport process is mediated by specialized viral movement proteins, which in same cases are membrane proteins, that drive the viral genome to the cellular membrane in order to be transported into neighbouring uninfected host cells through the plasmodesmal channel. We are currently investigating the targeting and the insertion mechanisms of these viral membrane proteins into the biological membranes.[Read more][Hide]
Web:
Scientific-technical goals: - Our Group focuses on basic aspects of the folding and assembly of proteins in lipid membranes.
Research lines: - Membrane Protein assembly.Our goal is to explore the mechanistic principles of membrane protein insertion, folding and assembly into lipid membranes and to investigate the factors that determine membrane protein stability.
- Membrane Protein proteomics.Overexpression of membrane proteins is often essential for structural and functional studies, but yields are frequently too low. Therefore, we investigate the consequences of overexpression of different membrane proteins in search for new components to improve such yields.
Group members:
CNAE:
Associated structure: - ERI Biotechnology and Biomedicine (BIOTECMED)
Keywords: - Transmembrane helices; Membrane Proteins; Protein Folding; Membrane Topology; Membrane Insertion
- Proteomics; Chaperone; Membrane Protein production; Optimization of protein expression
