3F1J

Crystal structure of the Borna disease virus matrix protein (BDV-M) reveals RNA binding properties

3F1J の概要

• エントリーDOI: 10.2210/pdb3f1j/pdb
• 分子名称: Matrix protein, CYTIDINE-5'-MONOPHOSPHATE, SULFATE ION, ... (4 entities in total)
• 機能のキーワード: viral matrix protein, rna binding, membrane binding, viruses, ssrna negative-strand viruses, mononegavirales; bornaviridae, bornavirus, alternative splicing, cytoplasm, virion, viral protein
• 由来する生物種: Borna disease virus (BDV)
• 細胞内の位置: Virion (Potential): P52637
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 16983.00

構造登録者

Neumann, P.,Lieber, D.,Meyer, S.,Dautel, P.,Kerth, A.,Kraus, I.,Garten, W.,Stubbs, M.T. (登録日: 2008-10-28, 公開日: 2009-02-03, 最終更新日: 2024-11-13)

主引用文献

Neumann, P.,Lieber, D.,Meyer, S.,Dautel, P.,Kerth, A.,Kraus, I.,Garten, W.,Stubbs, M.T.
Crystal structure of the Borna disease virus matrix protein (BDV-M) reveals ssRNA binding properties
Proc.Natl.Acad.Sci.USA, 106:3710-3715, 2009

PubMed Abstract: Borna disease virus (BDV) is a neurotropic enveloped RNA virus that causes a noncytolytic, persistent infection of the central nervous system in mammals. BDV belongs to the order Mononegavirales, which also includes the negative-strand RNA viruses (NSVs) Ebola, Marburg, vesicular stomatitis, rabies, mumps, and measles. BDV-M, the matrix protein (M-protein) of BDV, is the smallest M-protein (16.2 kDa) among the NSVs. M-proteins play a critical role in virus assembly and budding, mediating the interaction between the viral capsid, envelope, and glycoprotein spikes, and are as such responsible for the structural stability and individual form of virus particles. Here, we report the 3D structure of BDV-M, a full-length M-protein structure from a nonsegmented RNA NSV. The BDV-M monomer exhibits structural similarity to the N-terminal domain of the Ebola M-protein (VP40), while the surface charge of the tetramer provides clues to the membrane association of BDV-M. Additional electron density in the crystal reveals the presence of bound nucleic acid, interpreted as cytidine-5'-monophosphate. The heterologously expressed BDV-M copurifies with and protects ssRNA oligonucleotides of a median length of 16 nt taken up from the expression host. The results presented here show that BDV-M would be able to bind RNA and lipid membranes simultaneously, expanding the repertoire of M-protein functionalities.

PubMed: 19237566
DOI: 10.1073/pnas.0808101106

実験手法

X-RAY DIFFRACTION (2.65 Å)