-
Je něco špatně v tomto záznamu ?
Comparison of a retroviral protease in monomeric and dimeric states
S. Wosicki, M. Gilski, H. Zabranska, I. Pichova, M. Jaskolski,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu srovnávací studie, časopisecké články
Grantová podpora
RVO 61388963
Akademie Věd České Republiky
- MeSH
- endopeptidasy chemie genetika MeSH
- inhibitory proteas chemie MeSH
- kvarterní struktura proteinů * MeSH
- Masonův-Pfizerův opičí virus enzymologie MeSH
- multimerizace proteinu * MeSH
- mutace MeSH
- peptidomimetika chemie MeSH
- Publikační typ
- časopisecké články MeSH
- srovnávací studie MeSH
Retroviral proteases (RPs) are of high interest owing to their crucial role in the maturation process of retroviral particles. RPs are obligatory homodimers, with a pepsin-like active site built around two aspartates (in DTG triads) that activate a water molecule, as the nucleophile, under two flap loops. Mason-Pfizer monkey virus (M-PMV) is unique among retroviruses as its protease is also stable in the monomeric form, as confirmed by an existing crystal structure of a 13 kDa variant of the protein (M-PMV PR) and its previous biochemical characterization. In the present work, two mutants of M-PMV PR, D26N and C7A/D26N/C106A, were crystallized in complex with a peptidomimetic inhibitor and one mutant (D26N) was crystallized without the inhibitor. The crystal structures were solved at resolutions of 1.6, 1.9 and 2.0 Å, respectively. At variance with the previous study, all of the new structures have the canonical dimeric form of retroviral proteases. The protomers within a dimer differ mainly in the flap-loop region, with the most extreme case observed in the apo structure, in which one flap loop is well defined while the other flap loop is not defined by electron density. The presence of the inhibitor molecules in the complex structures was assessed using polder maps, but some details of their conformations remain ambiguous. In all of the presented structures the active site contains a water molecule buried deeply between the Asn26-Thr27-Gly28 triads of the protomers. Such a water molecule is completely unique not only in retropepsins but also in aspartic proteases in general. The C7A and C106A mutations do not influence the conformation of the protein. The Cys106 residue is properly placed at the homodimer interface area for a disulfide cross-link, but the reducing conditions of the crystallization experiment prevented S-S bond formation. An animated Interactive 3D Complement (I3DC) is available in Proteopedia at http://proteopedia.org/w/Journal:Acta_Cryst_D:S2059798319011355.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc20005822
- 003
- CZ-PrNML
- 005
- 20200528094218.0
- 007
- ta
- 008
- 200511s2019 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1107/S2059798319011355 $2 doi
- 035 __
- $a (PubMed)31588922
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Wosicki, Stanislaw $u Center for Biocrystallographic Research, Institute of Bioorganic Chemistry, Polish Academy of Sciences, 61-704 Poznan, Poland.
- 245 10
- $a Comparison of a retroviral protease in monomeric and dimeric states / $c S. Wosicki, M. Gilski, H. Zabranska, I. Pichova, M. Jaskolski,
- 520 9_
- $a Retroviral proteases (RPs) are of high interest owing to their crucial role in the maturation process of retroviral particles. RPs are obligatory homodimers, with a pepsin-like active site built around two aspartates (in DTG triads) that activate a water molecule, as the nucleophile, under two flap loops. Mason-Pfizer monkey virus (M-PMV) is unique among retroviruses as its protease is also stable in the monomeric form, as confirmed by an existing crystal structure of a 13 kDa variant of the protein (M-PMV PR) and its previous biochemical characterization. In the present work, two mutants of M-PMV PR, D26N and C7A/D26N/C106A, were crystallized in complex with a peptidomimetic inhibitor and one mutant (D26N) was crystallized without the inhibitor. The crystal structures were solved at resolutions of 1.6, 1.9 and 2.0 Å, respectively. At variance with the previous study, all of the new structures have the canonical dimeric form of retroviral proteases. The protomers within a dimer differ mainly in the flap-loop region, with the most extreme case observed in the apo structure, in which one flap loop is well defined while the other flap loop is not defined by electron density. The presence of the inhibitor molecules in the complex structures was assessed using polder maps, but some details of their conformations remain ambiguous. In all of the presented structures the active site contains a water molecule buried deeply between the Asn26-Thr27-Gly28 triads of the protomers. Such a water molecule is completely unique not only in retropepsins but also in aspartic proteases in general. The C7A and C106A mutations do not influence the conformation of the protein. The Cys106 residue is properly placed at the homodimer interface area for a disulfide cross-link, but the reducing conditions of the crystallization experiment prevented S-S bond formation. An animated Interactive 3D Complement (I3DC) is available in Proteopedia at http://proteopedia.org/w/Journal:Acta_Cryst_D:S2059798319011355.
- 650 _2
- $a endopeptidasy $x chemie $x genetika $7 D010450
- 650 _2
- $a Masonův-Pfizerův opičí virus $x enzymologie $7 D016093
- 650 _2
- $a mutace $7 D009154
- 650 _2
- $a peptidomimetika $x chemie $7 D057786
- 650 _2
- $a inhibitory proteas $x chemie $7 D011480
- 650 12
- $a multimerizace proteinu $7 D055503
- 650 12
- $a kvarterní struktura proteinů $7 D020836
- 655 _2
- $a srovnávací studie $7 D003160
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Gilski, Miroslaw $u Center for Biocrystallographic Research, Institute of Bioorganic Chemistry, Polish Academy of Sciences, 61-704 Poznan, Poland.
- 700 1_
- $a Zabranska, Helena $u Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, 166 10 Prague, Czech Republic.
- 700 1_
- $a Pichova, Iva $u Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, 166 10 Prague, Czech Republic.
- 700 1_
- $a Jaskolski, Mariusz $u Center for Biocrystallographic Research, Institute of Bioorganic Chemistry, Polish Academy of Sciences, 61-704 Poznan, Poland.
- 773 0_
- $w MED00195158 $t Acta crystallographica. Section D, Structural biology $x 2059-7983 $g Roč. 75, č. Pt 10 (2019), s. 904-917
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/31588922 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20200511 $b ABA008
- 991 __
- $a 20200528094216 $b ABA008
- 999 __
- $a ok $b bmc $g 1524680 $s 1095878
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2019 $b 75 $c Pt 10 $d 904-917 $e 20190920 $i 2059-7983 $m Acta crystallographica. Section D, Structural biology $n Acta Crystallogr D Struct Biol $x MED00195158
- GRA __
- $a RVO 61388963 $p Akademie Věd České Republiky
- LZP __
- $a Pubmed-20200511