izpis_h1_title_alt

Structural basis for the unique molecular properties of broad-range phospholipase C from Listeria monocytogenes
ID Petrišič, Nejc (Author), ID Adamek, Maksimiljan (Author), ID Kežar, Andreja (Author), ID Hočevar, Samo B. (Author), ID Žagar, Ema (Author), ID Anderluh, Gregor (Author), ID Podobnik, Marjetka (Author)

.pdfPDF - Presentation file, Download (4,53 MB)
MD5: 67CE68830134B0117362FAC2BCD2103E
URLURL - Source URL, Visit https://www.nature.com/articles/s41467-023-42134-4 This link opens in a new window

Abstract
Listeriosis is one of the most serious foodborne diseases caused by the intracellular bacterium Listeria monocytogenes. Its two major virulence factors, broad-range phospholipase C (LmPC-PLC) and the pore-forming toxin listeriolysin O (LLO), enable the bacterium to spread in the host by destroying cell membranes. Here, we determine the crystal structure of LmPC-PLC and complement it with the functional analysis of this enzyme. This reveals that LmPC-PLC has evolved several structural features to regulate its activity, including the invariant position of the N-terminal tryptophan (W1), the structurally plastic active site, Zn$^{2+}$-dependent activity, and the tendency to form oligomers with impaired enzymatic activity. We demonstrate that the enzymatic activity of LmPC-PLC can be specifically inhibited by its propeptide added in trans. Furthermore, we show that the phospholipase activity of LmPC-PLC facilitates the pore-forming activity of LLO and affects the morphology of LLO oligomerization on lipid membranes, revealing the multifaceted synergy of the two virulence factors.

Language:English
Keywords:hydrolases, pathogens, X-ray crystallography
Work type:Article
Typology:1.01 - Original Scientific Article
Organization:BF - Biotechnical Faculty
Publication status:Published
Publication version:Version of Record
Year:2023
Number of pages:17 str.
Numbering:Vol. 14, art. 6474
PID:20.500.12556/RUL-164449 This link opens in a new window
UDC:577
ISSN on article:2041-1723
DOI:10.1038/s41467-023-42134-4 This link opens in a new window
COBISS.SI-ID:170720003 This link opens in a new window
Publication date in RUL:25.10.2024
Views:71
Downloads:20
Metadata:XML DC-XML DC-RDF
:
Copy citation
Share:Bookmark and Share

Record is a part of a journal

Title:Nature communications
Shortened title:Nat. commun.
Publisher:Springer Nature
ISSN:2041-1723
COBISS.SI-ID:2315876 This link opens in a new window

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.

Secondary language

Language:Slovenian
Keywords:biokemija, listerioza, virulentnost, bakterije

Projects

Funder:ARRS - Slovenian Research Agency
Project number:J1-9174
Name:Mehanizem delovanja in sodelovanja treh ključnih listerijskih virulentnih faktorjev

Funder:ARRS - Slovenian Research Agency
Project number:P1-0391
Name:Molekulske interakcije

Funder:ARRS - Slovenian Research Agency
Project number:P2-0145
Name:Polimeri in polimerni materiali s posebnimi lastnostmi

Funder:ARRS - Slovenian Research Agency
Project number:P1-0034
Name:Analitika in kemijska karakterizacija materialov ter procesov

Funder:ARRS - Slovenian Research Agency
Project number:I0-0003
Name:Infrastrukturna dejavnost KI

Funder:ARRS - Slovenian Research Agency
Funding programme:Young researchers

Similar documents

Similar works from RUL:
Similar works from other Slovenian collections:

Back