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Pregled bibliografske jedinice broj: 916814

Crystal structure of dipeptidyl peptidase III from the human gut symbiont Bacteroides thetaiotaomicron


Sabljić, Igor; Meštrović Radan, Nevenka; Vukelić, Bojana; Macheroux, Peter; Gruber, Karl; Luić, Marija; Abramić, Marija
Crystal structure of dipeptidyl peptidase III from the human gut symbiont Bacteroides thetaiotaomicron // PLoS One, 12 (2017), 11; e0187295, 19 doi:10.1371/journal.pone.0187295 (međunarodna recenzija, članak, znanstveni)


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Naslov
Crystal structure of dipeptidyl peptidase III from the human gut symbiont Bacteroides thetaiotaomicron

Autori
Sabljić, Igor ; Meštrović Radan, Nevenka ; Vukelić, Bojana ; Macheroux, Peter ; Gruber, Karl ; Luić, Marija ; Abramić, Marija

Izvornik
PLoS One (1932-6203) 12 (2017), 11; E0187295, 19

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
dipeptidyl peptidase III ; Bacteroides thetaiotaomicron ; crystal structure ; peptidase family M49 ; zinc-dependent metallopeptidases ; DPP III

Sažetak
Bacteroides thetaiotaomicron is a dominant member of the human intestinal microbiome. The genome of this anaerobe encodes more than 100 proteolytic enzymes, the majority of which have not been characterized. In the present study, we have produced and purified recombinant dipeptidyl peptidase III (DPP III) from B. thetaiotaomicron for the purposes of biochemical and structural investigations. DPP III is a cytosolic zinc-metallopeptidase of the M49 family, involved in protein metabolism. The biochemical results for B. thetaiotaomicron DPP III from our research showed both some similarities to, as well as certain differences from, previously characterised yeast and human DPP III. The 3D-structure of B. thetaiotaomicron DPP III was determined by X-ray crystallography and revealed a two-domain protein. The ligand-free structure (refined to 2.4 Å) was in the open conformation, while in the presence of the hydroxamate inhibitor Tyr-Phe-NHOH, the closed form (refined to 3.3 Å) was observed. Compared to the closed form, the two domains of the open form are rotated away from each other by about 28 degrees. A comparison of the crystal structure of B. thetaiotaomicron DPP III with that of the human and yeast enzymes revealed a similar overall fold. However, a significant difference with functional implications was discovered in the upper domain, farther away from the catalytic centre. In addition, our data indicate that large protein flexibility might be conserved in the M49 family.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Projekti:
098-1191344-2938 - Molekularna enzimologija i proteinske interakcije hidrolaza (Abramić, Marija, MZOS ) ( POIROT)
EK-FP7-316289 - Enhancement of the Innovation Potential in SEE through new Molecular Solutions in Research and Development (INNOMOL) (Vugrek, Oliver, EK - FP7-REGPOT-2012-2013-1) ( POIROT)

Ustanove:
Institut "Ruđer Bošković", Zagreb

Poveznice na cjeloviti tekst rada:

doi fulir.irb.hr fulir.irb.hr journals.plos.org doi.org

Citiraj ovu publikaciju:

Sabljić, Igor; Meštrović Radan, Nevenka; Vukelić, Bojana; Macheroux, Peter; Gruber, Karl; Luić, Marija; Abramić, Marija
Crystal structure of dipeptidyl peptidase III from the human gut symbiont Bacteroides thetaiotaomicron // PLoS One, 12 (2017), 11; e0187295, 19 doi:10.1371/journal.pone.0187295 (međunarodna recenzija, članak, znanstveni)
Sabljić, I., Meštrović Radan, N., Vukelić, B., Macheroux, P., Gruber, K., Luić, M. & Abramić, M. (2017) Crystal structure of dipeptidyl peptidase III from the human gut symbiont Bacteroides thetaiotaomicron. PLoS One, 12 (11), e0187295, 19 doi:10.1371/journal.pone.0187295.
@article{article, year = {2017}, pages = {19}, DOI = {10.1371/journal.pone.0187295}, chapter = {e0187295}, keywords = {dipeptidyl peptidase III, Bacteroides thetaiotaomicron, crystal structure, peptidase family M49, zinc-dependent metallopeptidases, DPP III}, journal = {PLoS One}, doi = {10.1371/journal.pone.0187295}, volume = {12}, number = {11}, issn = {1932-6203}, title = {Crystal structure of dipeptidyl peptidase III from the human gut symbiont Bacteroides thetaiotaomicron}, keyword = {dipeptidyl peptidase III, Bacteroides thetaiotaomicron, crystal structure, peptidase family M49, zinc-dependent metallopeptidases, DPP III}, chapternumber = {e0187295} }
@article{article, year = {2017}, pages = {19}, DOI = {10.1371/journal.pone.0187295}, chapter = {e0187295}, keywords = {dipeptidyl peptidase III, Bacteroides thetaiotaomicron, crystal structure, peptidase family M49, zinc-dependent metallopeptidases, DPP III}, journal = {PLoS One}, doi = {10.1371/journal.pone.0187295}, volume = {12}, number = {11}, issn = {1932-6203}, title = {Crystal structure of dipeptidyl peptidase III from the human gut symbiont Bacteroides thetaiotaomicron}, keyword = {dipeptidyl peptidase III, Bacteroides thetaiotaomicron, crystal structure, peptidase family M49, zinc-dependent metallopeptidases, DPP III}, chapternumber = {e0187295} }

Časopis indeksira:


  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


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