Mechanism of Phosphatidylglycerol Activation Catalyzed by Prolipoprotein Diacylglyceryl Transferase

Singh, Warispreet, Bilal, Munir, McClory, James, Dourado, Daniel, Quinn, Derek, Moody, Thomas S., Sutcliffe, Iain and Huang, Meilan (2019) Mechanism of Phosphatidylglycerol Activation Catalyzed by Prolipoprotein Diacylglyceryl Transferase. The Journal of Physical Chemistry B, 123 (33). pp. 7092-7102. ISSN 1520-6106

[img] Text
Waris Bilal jp-2019-04227c.R2.pdf - Accepted Version
Restricted to Repository staff only until 7 August 2020.

Download (1MB) | Request a copy
Official URL: https://doi.org/10.1021/acs.jpcb.9b04227

Abstract

Lipoproteins are essential for bacterial survival. Bacterial lipoprotein biosynthesis is accomplished by sequential modification by three enzymes in the inner membrane, all of which are emerging antimicrobial targets. The X-ray crystal structure of prolipoprotein diacylglyceryl transferase (Lgt) and apolipoprotein N-acyl transferase (Lnt) has been reported. However, the mechanisms of the post-translational modification catalyzed by these enzymes have not been understood. Here, we studied the mechanism of the transacylation reaction catalyzed by Lgt, the first enzyme for lipoprotein modification using molecular docking, molecular dynamics, and quantum mechanics/molecular mechanics (QM/MM) calculations. Our results suggest that Arg143, Arg239, and Glu202 play a critical role in stabilizing the glycerol-1-phosphate head group and activating the glycerol C3–O ester bond of the phosphatidylglycerol (PG) substrate. With PG binding, the opening of the L6–7 loop mediated by the highly conserved Arg236 residue as a gatekeeper is observed, which facilitates the release of the modified lipoprotein product, as well as the entry of another PG substrate. Further QM/MM studies revealed that His103 acts as a catalytic base to abstract a proton from the cysteine residue of the preproliprotein, initiating the diacylglyceryl transfer from PG to preprolipoprotein. This is the first study on the mechanism of lipoprotein modification catalyzed by a post-translocational processing enzyme. The transacylation mechanism of Lgt would shed light on the development of novel antimicrobial therapies targeting the challenging enzymes involved in the post-translocational modification pathway of lipoproteins.

Item Type: Article
Subjects: F100 Chemistry
H800 Chemical, Process and Energy Engineering
Department: Faculties > Health and Life Sciences > Applied Sciences
Depositing User: Elena Carlaw
Date Deposited: 20 Aug 2019 10:17
Last Modified: 11 Oct 2019 13:04
URI: http://nrl.northumbria.ac.uk/id/eprint/40405

Actions (login required)

View Item View Item

Downloads

Downloads per month over past year

View more statistics


Policies: NRL Policies | NRL University Deposit Policy | NRL Deposit Licence