Structure and Function of the First Full-Length Murein Peptide Ligase (Mpl) Cell Wall Recycling Protein

Transcription

1 Paper Presentation PLoS ONE 2011 Structure and Function of the First Full-Length Murein Peptide Ligase (Mpl) Cell Wall Recycling Protein Debanu Das, Mireille Herve, Julie Feuerhelm, etc. and Dominique Mengin-Lecreulx*, lan A. Wilson* Hai Liang 11/20/2013

2 Paper Presentation PLoS ONE 2011 Structure and Function of the First Full-Length Murein Peptide Ligase (Mpl) Cell Wall Recycling Protein Debanu Das, Mireille Herve, Julie Feuerhelm, etc. and Dominique Mengin-Lecreulx*, lan A. Wilson* Hai Liang 11/20/2013

3 Background In the United States, about 30% of total waste is recycled in (data from Wikipedia) During each generation, ~30-60% of bacterial cell wall is recycled in Gramnegative bacteria. We should do better!!!

4 Background Bacterial cell wall What is peptidoglycan? Important bacterial cell wall component. Mesh-like layer outside the plasma membrane of bacteria. Structural strength, protection, osmotic pressure counteracting From Thomas M. Terry (2000).

5 Background Simplified model of G+ bacterial cell wall From en.wikipedia

6 Background Biosynthesis of peptidoglycan From Catherine Grimes

7 Background Biosynthesis of peptidoglycan What s the advantage of bacterial cell wall recycling? Some of these compounds are uneasy to make. If the bacteria decide to buy all the compounds they need from Sigma UDP-GlcNAc: $938.0/g L-Ala: $11.7/g D-Glu: $16.1/g A 2 pm: $2472.0/g D-Ala-D-Ala: $369.5/g From Jean van Heijenoort

8 Background Biosynthesis of peptidoglycan What s the advantage of bacterial cell wall recycling? Cell wall recycling would be beneficial in bacterial growth and give bacteria the advantage in competition with others. From Jean van Heijenoort

9 Background Peptidoglycan recycling pathway Mpl: Murein Peptide Ligase Important enzyme in cell wall recycling. Link the peptidoglycan breakdown component to UDP-MurNAc.

10 Background Experimental flowchart: 1. Mpl gene from Psychrobacter arcticus genome was cloned, and PaMpl protein was produced and crystallized. 2. MAD data were collected and protein structure was solved and refined. 3. Biochemical character and enzymatic activity of PaMpl were studied. Experiment methods: Polymerase Incomplete Primer Extension (PIPE) cloning method: In this method, all major cloning operations are achieved by transforming competent cells with PCR products immediately following amplification. Special PCR primers with overlapping sequences are used in this method.

11 Part 1. Crystal parameters, data collection and refinement statistics

12 Part 2. Sequence comparison of Mpl to MurC-F enzymes

13 Part 2. Sequence comparison of Mpl to MurC-F enzymes Sequence identity between Mpl and MurC is ~21 25%, between Mpl and MurD-F is ~15 17%. Overexpression of E. coli mpl gene was shown to complement an E. coli murc mutant.

14 Part 3. Overall structure analysis Secondary structure of PaMpl, based on domains and primary sequence. PaMpl can be divided into 3 distinct domains 1. N-terminal UDP-MurNAc-binding domain (ND, residues 1-102). 2. Middle ATP-binding domain (MD, residues ). 3. C-terminal tripeptide-binding domain (CD, residues ).

15 Results: Part 3. Overall structure analysis PaMpl is present as a monomer in crystal asymmetric unit. Ramachandran plot shows 98.1% of the residues are in the favored regions with none in disallowed regions. All three domains are linked to form a triangular-shaped molecule with dimensions of ~56X60X47 Å3. ND, residues MD, residues CD, residues

16 Part 4. Structure comparisons Comparison of crystal structures of full-length PaMpl (Blue) and truncated NmMpl (grey, ND and MD only, PDB 3eag). Sequence identity is 57%, R.m.s.d. is 2.2 Å over 311 Cα atoms. NmMpl lacks the segments (green), (orange) and (cyan). NmMpl residues are positioned differently compared to the PaMpl residues (yellow). PaMpl residues (red) are disordered.

17 Part 4. Structure comparisons Comparison of crystal structures of PaMpl (Blue), EcMurC (PDB 2f00, pale green), HiMurC (PDB 1p31, orange), and TmMurC (PDB 1j6u, grey). Results shows a common structural core of 355 Cα residues with an r.m.s.d. of 2.7 Å.

18 Part 4. Structure comparisons Surface representation of different domain dispositions in Mur family structure. A. apo-pampl. B. EcMurC with bound Mg 2+. C. HiMurC bound to UDP-MurNAc-L- Ala (UMA) and AMPPNP(ANP), and metal. D. Apo-EcMurF. These structures illustrate the conformational variability of these Mur enzymes. All molecules are in the same orientation. CD of the apo-pampl is rotated 30 when compared to MurC structure. ND, residues MD, residues CD, residues

19 Part 5. Oligomerization of PaMpl protein Static light scattering measurements indicated that a dimer form of PaMpl protein is prominent in solution. EcMpl is also dimeric in solution. EcMurD (PDB 1uag), EcMurE (PDB 1e8c) and EcMurF (PDB 1gg4), have been reported to be monomers in the crystal and in solution. EcMurC (PDB 2f00) is also a dimer in the crystal structure but in solution, displays a dynamic equilibrium between monomeric and dimeric forms. Both forms were active. Some residues in EcMurC which involved in dimerization are not found in PaMpl, which means the mode of dimerization in PaMpl may be different. Refractive index signal against elution time

20 Part 6. PaMpl residues involved in substrates interactions (ND and MD). Interactions between HiMurC and ligands UMA and ANP. Majority of these residues in HiMurC(red labels) ND and MD are conserved in PaMpl (blue labels). Mpl have similar interaction with ATP and UDP-MurNAc.

21 Part 6. PaMpl residues involved in substrates interactions. Mpl-specific residues in ND, MD and CD that may be involved in substrate interactions. Tyr35, Asn69, Arg73 and Gly74 are conserved residues in the vicinity of UDP-MurNAc-binding pocket. Tyr182 is unique to Mpl and located prior to the start of Mplspecific loop, it could be involved in substrate recognition. Tyr182, Gln223 and Phe224 are in the ATP-binding pocket. Glu181 will aid the stability of Mg2 binding.

22 Part 6. PaMpl residues involved in substrates interactions. CD of Mur families are functionally unique, they have the most variation in this domain. Arg357, Arg358, Phe374, Ala375, His376, His377, Glu402, Pro403, Arg404, Ser405, Asn406, Thr407, Ser483, Asn484 and Gly485 may be important in binding substrates. Based on their location, the CD should undergo a conformational change in the interaction with peptide.

23 Part 7. Enzymatic studies of PaMpl Kinetic parameters of PaMpl

24 Part 7. Enzymatic studies of PaMpl Substrate specificity of PaMpl Preference for A 2 pm at the third position.

25 Part 7. Enzymatic studies of PaMpl Optimal ph: 8.4 Optimal Mg concentration: 5mM Optimal temperature: 30 ºC At low temperature(~15 ºC), activity of PaMpl was almost twice that of EcMpl. And at 42 ºC, activity of PaMpl was almost completely abolished. Psychrobacter species are permafrost bacteria. EcMpl

26 Conclusion & Discussion 1. High-resolution crystal structure of the full-length PaMpl provides insights into the structure and relative orientations of the three domains in this cell wall recycling enzyme. 2. Various conserved Mpl residues which are potentially involved in substrate interaction provide a guide for site-directed mutagenesis to test their functional roles. 3. Temperature dependent manner of PaMpl is also a topic in future study. 4. Deletion of Mpl gene and other genes involved in peptidoglycan recycling could increase antibiotic susceptibility of some bacterial strains. In future the design of Mpl inhibitor turns to be possible based on the Mpl active sites.