Erized by X-ray crystallography [48]. CLMS has also contributed significantly to characterization

April 17, 2018

Erized by X-ray crystallography [48]. CLMS has also contributed significantly to characterization of the nuclear pore complex [49], the PP2A network [50], RNA polymerase II both in association with transcription factor IIF [51] and in the pre-initiation complex [52], the yeast SMC3/Scc1 interaction [32,53] and to mapping the interaction between microtubules and the structurally flexible Ska1 domain [54]. Here, we have used established template-based molecular modelling and a cross-link-constrained prediction strategy tailored to the characteristics of coiled-coil regions, to produce a low-resolution molecular structure of the SMC2/SMC4 core of the chicken condensin complex. Modelling of SMC2 and SMC4 head and hinge regions used several high-resolution crystal structures as templates. To model the lengthy antiparallel coiled-coils of SMC2 and SMC4 and determine their quaternary structure at low resolution, vital constraints on the structure were revealed through analysis of 120 crosslinks that were induced with bis(sulfosuccinimidyl)suberate (BS3) and mapped by mass spectrometry. Of those, 117 could be incorporated into our structure within the constraints imposed by the length of the cross-linker. The model presented here will be an important resource for future structureinformed mutagenesis and functional studies of vertebrate condensin in vitro and in vivo.rsob.royalsocietypublishing.org Open Biol. 5:3. Results3.1. Multiple cross-linked species of purified condensinOur studies employed two DT40 knockout cell lines expressing epitope-tagged condensin subunits: SMC2 knockout cells expressing streptavidin-binding peptide (SBP)-tagged SMC2 and CAP-H knockout cells expressing CAP-H-SBPGFP [29,55]. These tagged proteins are functional by the criterion of rescuing the life of the cells and are the only form of each protein expressed in the cells used. When DT40 mitotic cells were used to pull down SBP-tagged SMC2, the bound material consisted largely of an SMC2 and SMC4 subcomplex, with the non-SMC subunits not visible on denaturing gels (figure 1a). When the pulldown was performed using SBP-tagged CAP-H kleisin subunit, CAP-H was captured together with all other subunits of the condensin holocomplex (figure 1a). However, a significant proportion of the SMC2 and SMC4 remained in the supernatant (data not shown). These results purchase SB 203580 suggest that not all SMC2 and SMC4 in mitotic cells is present as canonical pentameric condensin complex. Indeed, Hirano et al. [25] identified an 8S condensin complex from Xenopus eggs as being composed of SMC2 and SMC4 and lacking the non-SMC subunits. Such a discrete SMC2/SMC4 complex was previously proposed to possess DNA re-annealing activity [56]. Treatment of the isolated holocomplex with the crosslinker bis(sulfosuccinimidyl)suberate (BS3), which prefers the primary amine lysine, but will also cross-link serine, threonine or tyrosine, resulted in the appearance of three new broad bands (i, ii and iii) in SDS AGE, regardless of the amount of cross-linker used (figure 1b, lanes 2?). Mass spectrometric characterization confirmed that each band(a) MWSMC2 –LonafarnibMedChemExpress Sch66336 SBPCAP-H -SBP(b) ratio ?5:[BS3] proteinrsob.royalsocietypublishing.org30 : 1 120 :kDa 170 130 100 70 55 40 35 25 1 1 SMC411,5 3 4,iii ii247 217 160 1,5 3 107 4,iOpen Biol. 5:3 3 SMC2 6 CAP-G 64 1 2 32 SMC2-SBP 5 CAP-D4 CAP-H-SBPFigure 1. Cross-linking of isolated condensin I complex. (a) Composition of condensin complex purified from mitotic DT40 cells using tagge.Erized by X-ray crystallography [48]. CLMS has also contributed significantly to characterization of the nuclear pore complex [49], the PP2A network [50], RNA polymerase II both in association with transcription factor IIF [51] and in the pre-initiation complex [52], the yeast SMC3/Scc1 interaction [32,53] and to mapping the interaction between microtubules and the structurally flexible Ska1 domain [54]. Here, we have used established template-based molecular modelling and a cross-link-constrained prediction strategy tailored to the characteristics of coiled-coil regions, to produce a low-resolution molecular structure of the SMC2/SMC4 core of the chicken condensin complex. Modelling of SMC2 and SMC4 head and hinge regions used several high-resolution crystal structures as templates. To model the lengthy antiparallel coiled-coils of SMC2 and SMC4 and determine their quaternary structure at low resolution, vital constraints on the structure were revealed through analysis of 120 crosslinks that were induced with bis(sulfosuccinimidyl)suberate (BS3) and mapped by mass spectrometry. Of those, 117 could be incorporated into our structure within the constraints imposed by the length of the cross-linker. The model presented here will be an important resource for future structureinformed mutagenesis and functional studies of vertebrate condensin in vitro and in vivo.rsob.royalsocietypublishing.org Open Biol. 5:3. Results3.1. Multiple cross-linked species of purified condensinOur studies employed two DT40 knockout cell lines expressing epitope-tagged condensin subunits: SMC2 knockout cells expressing streptavidin-binding peptide (SBP)-tagged SMC2 and CAP-H knockout cells expressing CAP-H-SBPGFP [29,55]. These tagged proteins are functional by the criterion of rescuing the life of the cells and are the only form of each protein expressed in the cells used. When DT40 mitotic cells were used to pull down SBP-tagged SMC2, the bound material consisted largely of an SMC2 and SMC4 subcomplex, with the non-SMC subunits not visible on denaturing gels (figure 1a). When the pulldown was performed using SBP-tagged CAP-H kleisin subunit, CAP-H was captured together with all other subunits of the condensin holocomplex (figure 1a). However, a significant proportion of the SMC2 and SMC4 remained in the supernatant (data not shown). These results suggest that not all SMC2 and SMC4 in mitotic cells is present as canonical pentameric condensin complex. Indeed, Hirano et al. [25] identified an 8S condensin complex from Xenopus eggs as being composed of SMC2 and SMC4 and lacking the non-SMC subunits. Such a discrete SMC2/SMC4 complex was previously proposed to possess DNA re-annealing activity [56]. Treatment of the isolated holocomplex with the crosslinker bis(sulfosuccinimidyl)suberate (BS3), which prefers the primary amine lysine, but will also cross-link serine, threonine or tyrosine, resulted in the appearance of three new broad bands (i, ii and iii) in SDS AGE, regardless of the amount of cross-linker used (figure 1b, lanes 2?). Mass spectrometric characterization confirmed that each band(a) MWSMC2 -SBPCAP-H -SBP(b) ratio ?5:[BS3] proteinrsob.royalsocietypublishing.org30 : 1 120 :kDa 170 130 100 70 55 40 35 25 1 1 SMC411,5 3 4,iii ii247 217 160 1,5 3 107 4,iOpen Biol. 5:3 3 SMC2 6 CAP-G 64 1 2 32 SMC2-SBP 5 CAP-D4 CAP-H-SBPFigure 1. Cross-linking of isolated condensin I complex. (a) Composition of condensin complex purified from mitotic DT40 cells using tagge.