2018
DOI: 10.1107/s2053230x18009706
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TssA from Burkholderia cenocepacia: expression, purification, crystallization and crystallographic analysis

Abstract: Analysis of the noncrystallographic symmetry of crystals of the C-terminal domain of Burkholderia cenocepacia TssA indicates a quaternary structure of 32 subunits in D 16 symmetry.

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“…Expression and purification of His 6 .TssA2 A (1–478), His 6 .TssA2 A Nt2 (223–387), His 6 .TssA2 A Nt2-CTD (223–478) and TssA2 A CTD (381–478) was carried out as previously described 33 . Both MBP.TssA1 B CTD (303–373) and His 6 .TssA1 B Nt1 (1–255) were overexpressed and purified, with TssA1 B CTD (303–373) being separated from the MBP solubility tag by Factor Xa cleavage 51 . MBP.TssA1 B CTD (294–373) was produced and purified in a similar manner as MBP.TssA1 B CTD (303–373).…”
Section: Methodsmentioning
confidence: 99%
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“…Expression and purification of His 6 .TssA2 A (1–478), His 6 .TssA2 A Nt2 (223–387), His 6 .TssA2 A Nt2-CTD (223–478) and TssA2 A CTD (381–478) was carried out as previously described 33 . Both MBP.TssA1 B CTD (303–373) and His 6 .TssA1 B Nt1 (1–255) were overexpressed and purified, with TssA1 B CTD (303–373) being separated from the MBP solubility tag by Factor Xa cleavage 51 . MBP.TssA1 B CTD (294–373) was produced and purified in a similar manner as MBP.TssA1 B CTD (303–373).…”
Section: Methodsmentioning
confidence: 99%
“…For crystallisation, MBP.His 6 .TssA1 B CTD H12–H14 (amino acids 303–358) was purified by amylose affinity chromatography, and eluted with 10 mM maltose. His 6 .TssA1 B CTD H12–H14 was proteolytically removed from the MBP tag by treatment with Factor Xa, followed by purification on a nickel column with imidazole gradient elution and SEC on a Superdex 200 column prior to concentration and final buffer exchange 51 .…”
Section: Methodsmentioning
confidence: 99%
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