ined from Invitrogen. HeLa cells were obtained from ATCC. Purification of His- or GST-tagged Proteins His-tagged proteins of His-p125, His-p50, His-p68, and Hisp12, Odanacatib expressed in E. coli BL21DE3, were purified by the use of nickel-nitrilotriacetic acid agarose and further purified by ion exchange chromatography on a FPLC Mono Q column as previously described. GST-tagged p12 in the pGEX-5X-3 vector was expressed in E. coli BL21DE3, and purified on glutathione beads . Non-tagged p12, used in reconstitution assays, was then released by proteolysis with Factor Xa, and the glutathione S-transferase was removed with glutathione-Sepharose. Generation of Recombinant Baculoviruses by the MultiBac System The coding regions for the human Pol d subunits p125, p50, p68, and p12 between the BamHI and XbaI sites in the pCDNA3.1-FLAG vector were excised and subcloned into the MCS1 multiple cloning site of the transfer vector pFBDM, in which each subunit was under the control of an individual polyhedrin gene promoter. The recombinant transfer vectors with different subunit assemblies were generated according to ��MultiBac Expression System User Manual”. The generated recombinant transfer vectors containing multi-subunit gene expression cassettes were introduced into MultiBac baculoviral DNA in DH10MultiBacCre E. coli cells which contain the factors for Tn7 transposition. Recombinant bacmids were generated in cells through the transposition of the Tn7 elements from the pFBDM derivative to the mini-attachment Tn7 target site on the bacmid DNA. Colonies containing bacmid carrying integrated cassettes were identified by blue/white screening and PCR analysis. Bacmid DNAs were prepared from selected white phenotype clones and Purification of Recombinant Human PCNA Human 
PCNA expressed in E. coli was purified using conventional chromatography as described previously, with minor modifications. The pTACTAC vector harboring human PCNA was expressed in one liter of DH5-a cell. Harvested cells were disrupted by sonication in lysis buffer. After centrifugation, the supernatant was chromatographed on a Q-sepharose column. The peak fractions containing PCNA were identified by Western blotting, Human DNA Polymerase Delta pooled, dialyzed against TGEED buffer, and further purified on a 4 ml Mono-P HR 5/20 column. Reconstitution of Pol d from the Core+p68 Trimer with Recombinant p12 Recombinant core+p68 was pre-incubated with different concentrations of non-tagged p12 at 4uC for 30 min before assay for the restoration of Pol d activity either on poly/oligo primer-template or singly primed M13 DNA template as described below. The native trimer lacking p12 used as a comparison was isolated from UV- treated HeLa cells. Expression and Purification of Recombinant Human Pol d and its Subassemblies A 600 ml suspension culture of Sf9 insect cells at 26106 cells/ ml was infected with recombinant baculoviruses at MOI of 2 for 72 hours. The cells were collected by centrifugation at 3,000 rpm for 5 minutes. The cell pellet was suspended in lysis buffer on ice for 30 minutes, PubMed ID:http://www.ncbi.nlm.nih.gov/pubmed/22188834 followed by sonication using 4615 second bursts with a 15 second cooling period between each burst and centrifugation at 15,000 rpm for 45 minutes. The supernatant was mixed with 10 ml of 78F5 anti-p125 immunoaffinity agarose beads with end to end rotation overnight and then loaded into a column. The column was washed with 10-bed volumes of TGEE buffer containing 0.1 M NaCl. Pol d was eluted using 5 bed volumes o
