메뉴 건너뛰기




Volumn 5, Issue 5, 2002, Pages 785-792

Novel approaches to antimicrobial therapy: Peptide deformylase

Author keywords

Antibacterial; Antimicrobial; BB 83698; Drug resistance; Peptide deformylase; Peptide deformylase inhibitors

Indexed keywords

ACTINONIN; BACTERIAL PROTEIN; CHLORAMPHENICOL; FORMYLMETHIONINE; MACROLIDE; METALLOPROTEINASE; N [1 TERT BUTYL 2 OXO 2 [4 (2 THIAZOLYLMETHYL) 1 PIPERAZINYL]ETHYL] 3 CYCLOPENTYL 2 (N FORMYL N HYDROXYAMINOMETHYL)PROPIONAMIDE; PEPTIDE DEFORMYLASE; PEPTIDE DEFORMYLASE INHIBITOR; POLYPEPTIDE; QUINOLINE DERIVED ANTIINFECTIVE AGENT; RIFAMPICIN; THIORPHAN; UNCLASSIFIED DRUG; VRC 4232; VRC 4307;

EID: 0036771389     PISSN: 13676733     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (51)

References (39)
  • 2
    • 0020321280 scopus 로고
    • Angiotensin-converting enzyme inhibitors: Medicinal chemistry and biological actions
    • Petrillo Jr EW, Ondetti MA: Angiotensin-converting enzyme inhibitors: Medicinal chemistry and biological actions. Med Res Rev (1982) 2(1):1-41
    • (1982) Med Res Rev , vol.2 , Issue.1 , pp. 1-41
    • Petrillo E.W., Jr.1    Ondetti, M.A.2
  • 3
    • 0030839472 scopus 로고    scopus 로고
    • Matrix metalloproteinase inhibition as a novel anticancer strategy: A review with special focus on Batimastat and Marimastat
    • Rasmussen HS, McCann PP: Matrix metalloproteinase inhibition as a novel anticancer strategy: A review with special focus on Batimastat and Marimastat. Pharmacol Ther (1997) 75(1):69-75.
    • (1997) Pharmacol Ther , vol.75 , Issue.1 , pp. 69-75
    • Rasmussen, H.S.1    McCann, P.P.2
  • 4
    • 0001651169 scopus 로고    scopus 로고
    • Design and therapeutic application of matrix metalloproteinase inhibitors
    • Whittaker M, Floyd CD, Brown P, Gearing AJ: Design and therapeutic application of matrix metalloproteinase inhibitors. Chem Rev (1999) 99(9):2735-2776.
    • (1999) Chem Rev , vol.99 , Issue.9 , pp. 2735-2776
    • Whittaker, M.1    Floyd, C.D.2    Brown, P.3    Gearing, A.J.4
  • 5
    • 0032766060 scopus 로고    scopus 로고
    • Processing of the N termini of nascent polypeptide chains requires deformylation prior to methionine removal
    • Solbiati J, Chapman-Smith A, Miller JL, Miller CG, Cronan Jr JE: Processing of the N termini of nascent polypeptide chains requires deformylation prior to methionine removal. J Mol Biol (1999) 290(3):607-614.
    • (1999) J Mol Biol , vol.290 , Issue.3 , pp. 607-614
    • Solbiati, J.1    Chapman-Smith, A.2    Miller, J.L.3    Miller, C.G.4    Cronan J.E., Jr.5
  • 6
    • 0024347025 scopus 로고
    • Methionine aminopeptidase gene of Escherichia coli is essential for cell growth
    • Chang SY, McGary EC, Chang S: Methionine aminopeptidase gene of Escherichia coli is essential for cell growth. J Bacteriol (1989) 171(7):4071-4072.
    • (1989) J Bacteriol , vol.171 , Issue.7 , pp. 4071-4072
    • Chang, S.Y.1    McGary, E.C.2    Chang, S.3
  • 7
    • 0028053015 scopus 로고
    • Genetic characterisation of polypeptide deformylase, a distinctive enzyme of eubacterial translation
    • Mazel D, Pochet S, Marliere P: Genetic characterisation of polypeptide deformylase, a distinctive enzyme of eubacterial translation. EMBO J (1994) 13(4):914-923.
    • (1994) EMBO J , vol.13 , Issue.4 , pp. 914-923
    • Mazel, D.1    Pochet, S.2    Marliere, P.3
  • 8
    • 0027369819 scopus 로고
    • Evidence that peptide deformylase and methionyl-tRNA (fMet) formyltransferase are encoded within the same operon in Escherichia coli
    • Meinnel T, Blanquet S: Evidence that peptide deformylase and methionyl-tRNA (fMet) formyltransferase are encoded within the same operon in Escherichia coli. J Bacteriol (1993) 175(23):7737-7740.
    • (1993) J Bacteriol , vol.175 , Issue.23 , pp. 7737-7740
    • Meinnel, T.1    Blanquet, S.2
  • 10
    • 0032540979 scopus 로고    scopus 로고
    • Control of peptide deformylase activity by metal cations
    • Ragusa S, Blanquet S, Meinnel T: Control of peptide deformylase activity by metal cations. J Mol Biol (1998) 280(3):515-523.
    • (1998) J Mol Biol , vol.280 , Issue.3 , pp. 515-523
    • Ragusa, S.1    Blanquet, S.2    Meinnel, T.3
  • 11
    • 0032575507 scopus 로고    scopus 로고
    • Oxygen-mediated inactivation of peptide deformylase
    • Rajagopalan PT, Pei D: Oxygen-mediated inactivation of peptide deformylase. J Biol Chem (1998) 273(35):22305-22310.
    • (1998) J Biol Chem , vol.273 , Issue.35 , pp. 22305-22310
    • Rajagopalan, P.T.1    Pei, D.2
  • 12
    • 0032496227 scopus 로고    scopus 로고
    • Structure of peptide deformylase and identification of the substrate binding site
    • Becker A, Schlichting I, Kabsch W, Schultz S, Wagner AF: Structure of peptide deformylase and identification of the substrate binding site. J Biol Chem (1998) 273(19):11413-11416.
    • (1998) J Biol Chem , vol.273 , Issue.19 , pp. 11413-11416
    • Becker, A.1    Schlichting, I.2    Kabsch, W.3    Schultz, S.4    Wagner, A.F.5
  • 13
  • 16
    • 0033547751 scopus 로고    scopus 로고
    • Determination of substrate specificity for peptide deformylase through the screening of a combinatorial peptide library
    • Hu YJ, Wei Y, Zhou Y, Rajagopalan PT, Pei D: Determination of substrate specificity for peptide deformylase through the screening of a combinatorial peptide library. Biochemistry (1999) 38(2):643-650.
    • (1999) Biochemistry , vol.38 , Issue.2 , pp. 643-650
    • Hu, Y.J.1    Wei, Y.2    Zhou, Y.3    Rajagopalan, P.T.4    Pei, D.5
  • 17
    • 0034681924 scopus 로고    scopus 로고
    • Synthesis and antibacterial activity of peptide deformylase inhibitors
    • Huntington KM, Yi T, Wei Y, Pei D: Synthesis and antibacterial activity of peptide deformylase inhibitors. Biochemistry (2000) 39(15):4543-4551.
    • (2000) Biochemistry , vol.39 , Issue.15 , pp. 4543-4551
    • Huntington, K.M.1    Yi, T.2    Wei, Y.3    Pei, D.4
  • 18
    • 0034322059 scopus 로고    scopus 로고
    • Identification of a potent peptide deformylase inhibitor from a rationally designed combinatorial library
    • Wei Y, Yi T, Huntington KM, Chaudhury C, Pei D: Identification of a potent peptide deformylase inhibitor from a rationally designed combinatorial library. J Comb Chem (2000) 2(6):650-657.
    • (2000) J Comb Chem , vol.2 , Issue.6 , pp. 650-657
    • Wei, Y.1    Yi, T.2    Huntington, K.M.3    Chaudhury, C.4    Pei, D.5
  • 19
    • 0033528708 scopus 로고    scopus 로고
    • Design and synthesis of substrate analogue inhibitors of peptide deformylase
    • Meinnel T, Patiny L, Ragusa S, Blanquet S: Design and synthesis of substrate analogue inhibitors of peptide deformylase. Biochemistry (1999) 38(14):4287-4295.
    • (1999) Biochemistry , vol.38 , Issue.14 , pp. 4287-4295
    • Meinnel, T.1    Patiny, L.2    Ragusa, S.3    Blanquet, S.4
  • 20
    • 0032712825 scopus 로고    scopus 로고
    • Developing a rational strategy for new antibacterial agents
    • Meinnel T: Developing a rational strategy for new antibacterial agents. Pathol Biol (Paris) (1999) 47(8):780-783.
    • (1999) Pathol Biol (Paris) , vol.47 , Issue.8 , pp. 780-783
    • Meinnel, T.1
  • 25
    • 0036210712 scopus 로고    scopus 로고
    • In vitro activities of peptide deformylase inhibitors against Gram-positive pathogens
    • Wise R, Andrews JM, Ashby J: In vitro activities of peptide deformylase inhibitors against Gram-positive pathogens. Antimicrob Agents Chemother (2002) 46(4):1117-1118.
    • (2002) Antimicrob Agents Chemother , vol.46 , Issue.4 , pp. 1117-1118
    • Wise, R.1    Andrews, J.M.2    Ashby, J.3
  • 26
    • 0346187348 scopus 로고    scopus 로고
    • In vivo pharmacodynamics of BB-83698, a deformylase inhibitor
    • Chicago, IL, USA:Abs F-355
    • Craig WA, Andes D: In vivo pharmacodynamics of BB-83698, a deformylase inhibitor. 41st ICAAC Meeting, Chicago, IL, USA (2001):Abs F-355. • Pharmacodynamic analysis of the first PDFI to enter rigorous testing in animal models of infection.
    • (2001) 41st ICAAC Meeting
    • Craig, W.A.1    Andes, D.2
  • 27
    • 0013396983 scopus 로고    scopus 로고
    • Efficacy of BB-83698, a novel peptide deformylase inhibitor, in a mouse pneumonia model induced by wild type and antimicrobial-resistant Streptococcus pneumoniae
    • Chicago, IL, USA:Abs F-354
    • Azoulay-Dupuis E, Mohler J, Rieux V, Bédos J, Moine P, Carbon C: Efficacy of BB-83698, a novel peptide deformylase inhibitor, in a mouse pneumonia model induced by wild type and antimicrobial-resistant Streptococcus pneumoniae. 41st ICAAC Meeting, Chicago, IL, USA (2001):Abs F-354. • Demonstration of in vivo efficacy of PDFIs in lethal RTI infections resistant to conventional antibiotics.
    • (2001) 41st ICAAC Meeting
    • Azoulay-Dupuis, E.1    Mohler, J.2    Rieux, V.3    Bédos, J.4    Moine, P.5    Carbon, C.6
  • 28
    • 0033919993 scopus 로고    scopus 로고
    • Peptide deformylase in Staphylococcus aureus: Resistance to inhibition is mediated by mutations in the formyltransferase gene
    • Margolis PS, Hackbarth CJ, Young DC, Wang W, Chen D, Yuan Z, White R, Trias J: Peptide deformylase in Staphylococcus aureus: Resistance to inhibition is mediated by mutations in the formyltransferase gene. Antimicrob Agents Chemother (2000) 44(7):1825-1831.
    • (2000) Antimicrob Agents Chemother , vol.44 , Issue.7 , pp. 1825-1831
    • Margolis, P.S.1    Hackbarth, C.J.2    Young, D.C.3    Wang, W.4    Chen, D.5    Yuan, Z.6    White, R.7    Trias, J.8
  • 29
    • 0034878770 scopus 로고    scopus 로고
    • Resistance of Streptococcus pneumoniae to deformylase inhibitors is due to mutations in defB
    • Margolis P, Hackbarth C, Lopez S, Maniar M, Wang W, Yuan Z, White R, Trias J: Resistance of Streptococcus pneumoniae to deformylase inhibitors is due to mutations in defB. Antimicrob Agents Chemother (2001) 45(9):2432-2435. •• Validates PDF as an excellent target in S pneumoniae and reviews PDF resistance mechanisms in other bacteria.
    • (2001) Antimicrob Agents Chemother , vol.45 , Issue.9 , pp. 2432-2435
    • Margolis, P.1    Hackbarth, C.2    Lopez, S.3    Maniar, M.4    Wang, W.5    Yuan, Z.6    White, R.7    Trias, J.8
  • 30
    • 0034329475 scopus 로고    scopus 로고
    • Identification of eukaryotic peptide deformylases reveals universality of N-terminal protein processing mechanisms
    • Giglione C, Serero A, Pierre M, Boisson B, Meinnel T: Identification of eukaryotic peptide deformylases reveals universality of N-terminal protein processing mechanisms. EMBO J (2000) 19(21):5916-5929. •• Discovery of eukaryotic PDF enzyme classes and their localization to cellular organelles.
    • (2000) EMBO J , vol.19 , Issue.21 , pp. 5916-5929
    • Giglione, C.1    Serero, A.2    Pierre, M.3    Boisson, B.4    Meinnel, T.5
  • 31
    • 0033936704 scopus 로고    scopus 로고
    • Peptide deformylase as a target for new generation, broad spectrum antimicrobial agents
    • Giglione C, Pierre M, Meinnel T: Peptide deformylase as a target for new generation, broad spectrum antimicrobial agents. Mol Microbiol (2000) 36(6):1197-1205.
    • (2000) Mol Microbiol , vol.36 , Issue.6 , pp. 1197-1205
    • Giglione, C.1    Pierre, M.2    Meinnel, T.3
  • 32
    • 0035824874 scopus 로고    scopus 로고
    • Distinctive features of the two classes of eukaryotic peptide deformylases
    • Serero A, Giglione C, Meinnel T: Distinctive features of the two classes of eukaryotic peptide deformylases. J Mol Biol (2001) 314(4):695-708. • Characterization and identification of differences between the two forms of PDF within Arabidopsis thaliana.
    • (2001) J Mol Biol , vol.314 , Issue.4 , pp. 695-708
    • Serero, A.1    Giglione, C.2    Meinnel, T.3
  • 33
    • 0002002492 scopus 로고    scopus 로고
    • Peptide deformylase as an emerging target for antiparasitic agents
    • Giglione C, Meinnel T: Peptide deformylase as an emerging target for antiparasitic agents. Exp Opin Ther Targets (2001) 5:41-57. •• Excellent review of the PDF enzyme class, including their catalytic mechanism and conservation in prokaryotic and eukaryotic organisms.
    • (2001) Exp Opin Ther Targets , vol.5 , pp. 41-57
    • Giglione, C.1    Meinnel, T.2
  • 34
    • 0013348409 scopus 로고    scopus 로고
    • In vivo evaluation of VRC3375, a potent peptide deformylase inhibitor
    • Toronto, ON, Canada:Abs 2175
    • Chen D, Hackbarth C, Ni ZJ, Wang W, Wu C, Young D, White RJ, Trias J, Patel DV, Yuan Z: In vivo evaluation of VRC3375, a potent peptide deformylase inhibitor. 40th ICAAC Meeting, Toronto, ON, Canada (2000):Abs 2175. • In vivo efficacy and selectivity of a potent PDF inhibitor, validating the use of PDFIs as therapeutic agents.
    • (2000) 40th ICAAC Meeting
    • Chen, D.1    Hackbarth, C.2    Ni, Z.J.3    Wang, W.4    Wu, C.5    Young, D.6    White, R.J.7    Trias, J.8    Patel, D.V.9    Yuan, Z.10
  • 35
    • 0035190394 scopus 로고    scopus 로고
    • Seeking new targets for antiparasitic agents
    • Wiesner J, Sanderbrand S, Altincicek B, Beck E, Jomaa H: Seeking new targets for antiparasitic agents. Trends Parasitol (2001) 17(1):7-8. • Provides evidence that selective PDFIs may have potential as antimalarial agents.
    • (2001) Trends Parasitol , vol.17 , Issue.1 , pp. 7-8
    • Wiesner, J.1    Sanderbrand, S.2    Altincicek, B.3    Beck, E.4    Jomaa, H.5
  • 36
    • 0036124280 scopus 로고    scopus 로고
    • Crystals of peptide deformylase from Plasmodium falciparum reveal critical characteristics of the active site for drug design
    • Kumar A, Nguyen KT, Srivathsan S, Omstein B, Turley S, Hirsh I, Pei D, Hol WG: Crystals of peptide deformylase from Plasmodium falciparum reveal critical characteristics of the active site for drug design. Structure (2002) 10(3):357-367.
    • (2002) Structure , vol.10 , Issue.3 , pp. 357-367
    • Kumar, A.1    Nguyen, K.T.2    Srivathsan, S.3    Omstein, B.4    Turley, S.5    Hirsh, I.6    Pei, D.7    Hol, W.G.8
  • 37
    • 0013438099 scopus 로고    scopus 로고
    • Methods for solid-phase synthesis of hydroxylamine compounds and derivatives, and combinatorial libraries thereof. WO-09957097 (1999)
    • VERSICOR INC (Patel DV): Methods for solid-phase synthesis of hydroxylamine compounds and derivatives, and combinatorial libraries thereof. WO-09957097 (1999).
    • Patel, D.V.1
  • 38
    • 0013348442 scopus 로고    scopus 로고
    • Novel urea compounds, compositions and methods of use and preparation. WO-00144178 (2001)
    • VERSICOR INC (Ni Z-J, Jacobs JW, Patel DV, Lewis J): Novel urea compounds, compositions and methods of use and preparation. WO-00144178 (2001).
    • Ni, Z.-J.1    Jacobs, J.W.2    Patel, D.V.3    Lewis, J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.