The Adeno-Associated Virus Replication Protein Rep78 Contains a Strictly C-Terminal Sequence Motif Conserved Across Dependoparvoviruses.

Viruses

Division Phytomedicine, Thaer-Institute of Agricultural and Horticultural Sciences, Humboldt-Universität zu Berlin, Lentzeallee 55/57, D-14195 Berlin, Germany.

Published: November 2024

Adeno-Associated Viruses (AAVs, genus ) are the leading gene therapy vector. Until recently, efforts to enhance their capacity for gene delivery had focused on their capsids. However, efforts are increasingly shifting towards improving the viral replication protein, Rep78. We discovered that Rep78 and its shorter isoform Rep52 contain a strictly C-terminal sequence motif, DDx3EQ, conserved in most dependoparvoviruses. The motif is highly negatively charged and devoid of prolines. Its wide conservation suggests that it is required for the life cycle of dependoparvoviruses. Despite its short length, the motif's strictly C-terminal position has the potential to endow it with a high recognition specificity. A candidate target of the DDx3EQ motif might be the DNA-binding interface of the origin-binding domain of Rep78, which is highly positively charged. Published studies suggest that this motif is not required for recombinant AAV production, but that substitutions within it might improve production.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11598897PMC
http://dx.doi.org/10.3390/v16111760DOI Listing

Publication Analysis

Top Keywords

strictly c-terminal
12
replication protein
8
protein rep78
8
c-terminal sequence
8
sequence motif
8
conserved dependoparvoviruses
8
motif
5
adeno-associated virus
4
virus replication
4
rep78
4

Similar Publications

Cleavage of Cartilage Oligomeric Matrix Protein (COMP) by ADAMTS4 generates a neoepitope associated with osteoarthritis and other forms of degenerative joint disease.

Matrix Biol

December 2024

Department of Immunology and Inflammation, Imperial College London, Du Cane Road, W12 0NN, London, United Kingdom;; Department of Biochemical Sciences, School of Biosciences, Faculty of Health and Medical Sciences, Edward Jenner Building, University of Surrey, Guildford, Surrey GU2 7XH, United Kingdom;. Electronic address:

Osteoarthritis (OA) is a highly prevalent joint disease, affecting millions of people worldwide and characterized by degradation of articular cartilage, subchondral bone remodeling and low-grade inflammation, leading to pain, stiffness and disability. Cartilage Oligomeric Matrix Protein (COMP) is a major structural component of cartilage and its degradation has been proposed as a marker of OA severity/progression. Several proteases cleave COMP in vitro, however, it is unclear which of these COMPase activities is prevalent in an osteoarthritic joint.

View Article and Find Full Text PDF

Comparative crystal structure analysis of the human EP300 and CBP KIX domains.

Biochem Biophys Res Commun

December 2024

Research Institute, National Cancer Center, Goyang-si, Gyeonggi-do, 10408, Republic of Korea; Department of Cancer Biomedical Science, National Cancer Center Graduate School of Cancer Science and Policy, Goyang-si, Gyeonggi-do, 10408, Republic of Korea. Electronic address:

Small-cell lung cancer (SCLC) is highly lethal because the tumors grow and metastasize rapidly. Effective treatments for SCLC are lacking currently. A recent study demonstrated that the E1A binding protein P300 (EP300) KIX domain has pro-tumorigenic activity and is selectively involved in the development and growth of SCLC.

View Article and Find Full Text PDF

The Adeno-Associated Virus Replication Protein Rep78 Contains a Strictly C-Terminal Sequence Motif Conserved Across Dependoparvoviruses.

Viruses

November 2024

Division Phytomedicine, Thaer-Institute of Agricultural and Horticultural Sciences, Humboldt-Universität zu Berlin, Lentzeallee 55/57, D-14195 Berlin, Germany.

Adeno-Associated Viruses (AAVs, genus ) are the leading gene therapy vector. Until recently, efforts to enhance their capacity for gene delivery had focused on their capsids. However, efforts are increasingly shifting towards improving the viral replication protein, Rep78.

View Article and Find Full Text PDF

Apolipoprotein-L1 (APOL1): From Sleeping Sickness to Kidney Disease.

Cells

October 2024

Laboratory of Molecular Parasitology, Institut de Biologie et de Médecine Moléculaires (IBMM), Université Libre de Bruxelles, 6041 Gosselies, Belgium.

Apolipoprotein-L1 (APOL1) is a membrane-interacting protein induced by inflammation, which confers human resistance to infection by African trypanosomes. APOL1 kills through induction of apoptotic-like parasite death, but two clones acquired resistance to APOL1, allowing them to cause sleeping sickness. An APOL1 C-terminal sequence alteration, such as occurs in natural West African variants G1 and G2, restored human resistance to these clones.

View Article and Find Full Text PDF
Article Synopsis
  • - Understanding the S-layer anchoring in bacteria involves non-covalent interactions between S-layer domains and secondary cell wall polymers (SCWPs), with specific roles for ManNAc ligands and the MnaA enzyme in SCWP biosynthesis.
  • - Research focused on producing MnaA and its variants to analyze their kinetic properties, test allosteric activation by UDP-GlcNAc, and explore the effects of tunicamycin as a potential inhibitor using crystal structure analysis and molecular docking.
  • - The study revealed the crystal structure of MnaA and confirmed the conservation of key residues, finding that UDP-GlcNAc boosts reaction rates but isn't essential for its function, while tunicamycin doesn't
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!