Xenopus embryos

Eggs were obtained from Xenopus laevis females (NASCO) after injection of 700–800 units of human chorionic gonadotropin. Frog handling was according to the animal protocol approved by the MSSM IACUC. In vitro fertilization, embryo culture in 0.1 x Marc’s modified Ringer (MMR) solution and staging were carried out as described [18–20]. Embryos were injected at the 4-cell stage with 100 pg of Ndel1 plasmid (25 pg per injection in each blastomere) and were cultured until stage 22 or 38 when they were lysed in 1% Triton X100, 50 mM NaCl, 1 mM EDTA and 10 mM Tris HCl (pH 7.5).

Construction of a nanobody phage display library from an immune llama

To prepare immunogen, a mixture of Xenopus laevis gastrula and neurula embryos was homogenized in 0.1 x MMR by pipetting and fractionated by centrifugation at 1800 g for 15 min. Several layers became visible after the fractionation, including yolk platelets, ‘pigmented and clear fractions’ and the lipid layer (from bottom to top). Whole blood was obtained from a llama (Triple J Farm, WA) immunized six times at 3-week intervals with the clear fraction of (approx. 200 micrograms of protein per injection), which contains cytoplasm, membranes as well as nuclei, as previously described [21]. The blood diluted with PBS was layered on top of Lympholyte (Cedarlane) and centrifuged at 800 g for 20 min to collect white blood cells at the interface. Total RNA was extracted from white blood cells using RNAeasy miniprep kit (Qiagen). 18 μg of total RNA was obtained from 5 x 10⁷ cells and used to synthesize cDNA with first strand cDNA synthesis kit (Superscript II, Invitrogen), following manufacturer’s instructions. DNA fragments corresponding to variable heavy chain (VHH or nanobody) were amplified from the cDNA with Pfu DNA polymerase and nested primers designed as described [11, 22] with modifications. The first PCR was performed with the following two sets of primers.

Ryc-Fw 1, 5’ GTCCTGGCTGCTCTTCTACAAGG 3’ and

Ryc-Rv 1, 5’ GGTACGTGCTGTTGAACTGTTCC 3’;

Lad-Fw 1, 5’ GAK GTS CAG CTG CAG GCG TCT GGR GGA GG 3’ and

Lad-Rv 1, 5’ CGC CAT CAA GGT ACC AGT TGA 3’.

The PCR products (600–800 bp) were gel purified and subjected to a second nested PCR with two sets of primers as follows. Ryc-Fw 3, 5’ ATG GCC CAG CCG GCC GTG CAG CTG GTG GAG TCT G 3’ and Ryc-Rv 2, 5’ TTA TGC GGC CGC CGA GGA GAC GGT GAC CTG GGT 3’; Lad-Fw 3, 5’ ATG GCC CAG CCG GCC GAK GTS CAG CTG CAG GCG 3’ and Lad-Rv-2, 5’ AT TGC GGC CGC TGA GGA GAC GGT GAC CTG 3’. Final PCR products of 350–450 bp (50 μg) and the phage display vector, pecan126 (48 μg) that endows sdAb with biotinylation acceptor peptide, His⁶-tag, and optional M13 phage gene 3 fusion [23] were digested with Sfi I and Not I, treated with calf intestinal phosphatase CIP, gel purified and ligated with T4 DNA ligase. The ligated material (300 μl) was extracted with phenol/chloroform and chloroform, ethanol precipitated and dissolved in 60–120 μl H₂O for electroporation into HBV88 cells.

HBV88 cells contain a chloramphenicol-resistant plasmid encoding a suppressor tRNA which is expressed upon arabinose induction [23]. The cells were made electrocompetent using low salt YENB media followed by extensive washing as described [23]. Bacteria were streaked on M9/chloramphenicol (Cm) + thiamine M9 minimal agar to select for the F’-episome. A single colony was cultured first in 2 ml of liquid M9 media for 8 h. 200 μl of the culture was added to 2 x 50 ml liquid M9 and shaken overnight at 37⁰ C. 10 ml of the culture was added to 6 x 400 ml flasks of YENB plus Cm to OD₆₀₀ = 0.05 and shaken at 30⁰ C until OD = 0.6 (approx. 5 h). After chilling on ice, the cultures were pelleted in Sorvall RC3C+ centrifuge at 4000 g at 4°C for 20 min. Each pellet from 6 preparations was resuspended gently in 50 ml ice-cold water and transferred into 2 x 50 ml conical tubes. Ice-cold water was added to 50 ml and mixed. Cells were pelleted at 4000 g at 4°C for 15 min. This washing procedure was repeated. Cells were further washed in 25 ml of ice-cold 15% glycerol, pelleted again and resuspended in 8.7 ml of 15% glycerol. Competent cells were aliquoted at 270 μl into Eppendorf tubes (pre-chilled), frozen in dry ice and stored at -80°C. Transformation efficiency was 5.2 x 10⁸ CFU/μg with pecan126 plasmid.

For electroporation using Gene Pulser (Bio-Rad), 60–90 μl of the ligated material and 270 μl of electrocompetent HVB88 cells were mixed, placed into a 2 mm-gap cuvette (BioRad or Bulldog Bio) and received a 2.5 kV pulse at 25 μF and 200 Ω. The electroporated cells were added to 2 ml of warm (37°C) super optimal broth (SOB) + 2% glucose in a 15 ml tube and incubated on a platform shaker at 37 ⁰C for 1 h. The culture was centrifuged at 3000 rpm for 10 min. The pellets were resuspended in 500 μl SOB+2% glucose and each suspension was spread onto two 15 cm 2 x YT + 2% glucose plates (Cm and 200 μg/ml ampicillin [Amp])). The plates were incubated at 37°C overnight. Approximately 10⁸ transformants were obtained with the transformation efficiency of 2x10⁶ CFU/μg. All colonies were collected in 70 ml of 2 x YT + 2% glucose media and an equal volume (70 ml) of ice cold 30% glycerol in Terrific Broth was added and mixed well. 1.3 ml aliquots in Eppendorf tubes were frozen on dry ice and stored at -80°C.

The pecan126 library was rescued as described [23]. 430 μl of the thawed HBV88 library stock were added to 500 ml 2x YT 2% glucose (Amp, Cm) to make an OD₆₀₀ = 0.05, and cultured until OD₆₀₀ = 0.44 was reached (approximately 2 h at 37°C). Helper phage M13K07 was added at a multiplicity of infection (MOI) of 20 to the culture and incubated static at 37 ⁰C for 30 min and then shaken at 200 rpm for 30 min at 37 ^oC. L-Arabinose (2000 μg/ml, final), IPTG (10 μM) and kanamycin (70 μg/ml) were added to the culture, which was shaken at 30 ⁰ C for 22 h. The culture was transferred to 16 round bottom 30 ml tubes (for high speed centrifugation) and centrifuged with Sorvall 5C Plus at 7700 g for 1 h at 4 ⁰C. 100 ml of 20% PEG8000+ 2.5 M NaCl were added to the supernatant and stirred at 4 ⁰C overnight. 600 ml of the phage were centrifuged at 4100 g for 1 h at 4 ⁰C. The pellets were resuspended in 3.3 ml of PBS, mixed with 3.3 ml of glycerol and aliquoted at 500 μl for storage at -80⁰ C. The titer of the phage library was 3.6 x 10¹⁰ cfu/ml. The nanobody DNA sequences reported in this paper are presented in S1 Fig.

Phage display screen using the immune llama cDNA library

Ten to twenty embryos at stage 11 and 14 were fixed with 3.7% formaldehyde in PBS for 1 h and subsequently with Dent’s fixative (80% methanol and 20% DMSO) for 1 h. The fixed embryos were washed with PBS three times and homogenized with a pestle after adding 50 μl PBS in 1.5 ml Eppendorf tubes. 2% skim milk in PBS (1 ml) was added to the tubes and rocked on a nutator for 1 h at room temperature. 600 μl of 2% skim milk was added to 200 μl of the rescued pecan126 phage library and rocked for 1 h to block nonspecific phage binding. The blocked phage library aliquot was split into two tubes containing stage 11 and 14 embryo homogenates and rocked for 1 h. These two tubes were centrifuged at 1000 g for 1 min to precipitate the particulate material containing the bound phages, whereas the supernatant was discarded. After washing ten times with PBS and another ten times with PBS with 0.1% Tween 20 (PBS-T), bound phages were eluted with 200 μl of 100 mM triethylamine by rocking for 9 min. After centrifugation at 100 g for 1 min, the supernatant was transferred to tubes that contain 100 μl of 1 M Tris-HCl (pH 7.5) to neutralize the triethylamine. 150 μl of the mixture containing eluted phage was infected into 10 ml of HBV88 cells that had been cultured with Cm to OD₆₀₀ = 0.8. The infection was performed static at 37°C for 30 min. The infected bacteria were collected and spread on a 15 cm plate of 1.5% agar in 2 x YT + Amp and Cm with 10 times dilution or on another plate without dilution to obtain isolated colonies. 40 pools of 20 colonies were made from stage 11 or stage 14 phage display group. Periplasm was prepared from these pools as described below.

To deploy the phage for Western blot membrane probing, lysates from stage 11, 15 and 26 embryos were resolved on 10% SDS-PAGE and transferred to PVDF membrane (1.2 embryo equivalents per lane) as described below [24]. The PVDF membrane was cut into pieces, incubated with 2% skim milk in PBS for blocking for 30 min and washed with PBS three times. 30 μl of the pecan126 phage library was incubated in 5 ml of 2% skim milk in PBS for blocking for 30 min. The phage library mixture was divided into three and added to three pieces of the blocked membrane. After the incubation for 1 h, the membranes were washed with PBS 10 times and subsequently with PBS-T 10 times. Bound phages were eluted with 1.5 ml of 100 mM triethylamine by incubating for 9 min. The eluted phage was neutralized with 0.75 ml of 1 M Tris (pH 7.5). 375 μl of phage eluates from three stages were used to infect 10 ml of HBV88 cells that were grown to OD₆₀₀ = 0.46 in LB + Cm and left static at 37^o C for 30 min. The infected bacteria were spread on one 9 cm plate without dilution and another plate after 10-fold dilution to obtain isolated colonies. 20 pools of 10 colonies each were made for each phage preparation.

Phage display screen of semi-synthetic llama nanobody library

Nomad#1 library consists of hyperdiversified nanobody genes originally isolated from three unimmunized llamas in pecan21 phage display vector that fuses the antibody to M13 gene 3 [25]. Ndel1-MBP consists of the N-terminal 242 amino acids of Xenopus Ndel1 fused to maltose binding protein (MBP). LIS1-MBP consists of the N-terminal 90 amino acids of Xenopus LIS1 fused to MBP. Both MBP fusions were provided by Victoria J. Allan (University of Manchester). Conventional panning methods were used for these targets [26]. An 8-well strip with high binding capacity (Costar) was coated with 8 x100 μl of 10 μg/ml of Ndel1-MBP or LIS1-MBP proteins overnight at 4°C. The coated wells were washed with PBS three times and blocked with 2% skim milk in PBS for 1 h. 80 μl of Nomad1 phage library (1 x 10¹² cfu/ml) was diluted 10 times with 2% skim milk in PBS and incubated for 1 hour for blocking. For phage panning using Ndel1-MBP, 800 μl of the diluted phage library was preincubated with 8 μg of LIS1-MBP, while for phage display to LIS1-MBP, the diluted phage library was preincubated with 8 μg of Ndel1-MBP to eliminate anti-MBP binders. 8 x 100 μl of the preincubated phage library was added to 8 wells and incubated on a nutator for 1 h and subsequently static for 1 h. After the incubations, the 8-well strips were washed with PBS-T 10 times and PBS 10 times. 8 x 100 μl of 100 mM triethylamine was added to the 8 well strip and incubated for 10 min for eluting phages. The eluted phages were collected and neutralized with 400 μl of 1 M Tris (pH 7.5). 600 μl of the neutralized phage eluates were infected into 10 ml of mid-exponential phase XL1-Blue in 2 x YT/2% glucose with 30 μg/ml tetracycline (Tet) for 30 min at 37°C. An aliquot of the infected bacteria was serially diluted (1/10, 1/100, 1/1000) and spread on 10 cm plates for titer check and for obtaining single colonies to prepare monoclonal phages. The rest of the infected bacteria were gently pelleted and spread on 15 cm plates. The plates were incubated overnight at 37°C.

Bacterial colonies on 15 cm plates were collected with 3 ml 2 x YT/2% glucose with scraper. 900 μl of the bacterial suspension was mixed with 900 μl of 2 x YT/30% glycerol and stored at -80°C. 800 μl of the suspension was added to 40 ml of 2 x YT/2% glucose with Amp/Tet to obtain an OD₆₀₀ = 0.1 and incubated for 1 h, followed by adding M13K07 helper phage at an MOI of 20 and incubating static for 1 hour at 37 ^oC. The bacterial culture was further incubated with kanamycin (final 70 μg/ml) and IPTG (1 mM final) overnight on a shaker at 30°C to rescue phage. 2 ml of the culture was centrifuged at 14000 rpm for 1 min and 800 μl of the supernatant containing rescued phage was mixed with 200 μl of 10% skim milk in PBS for the next round of panning. The rest of the phage was kept at -80 ^oC for polyclonal ELISA. For the second round of panning, 8-well strips were coated with 10 μg/ml of Ndel1-MBP and LIS1-MBP, but washing after phage incubation was performed with PBS-T and PBS (20 times each). For the third and fourth rounds of panning, 8 well strips were coated with 1 μg/ml of Ndel1-MBP and LIS1-MBP and washing was performed with PBS-T and PBS (40 times each).

For monoclonal phage preparation, single colonies with phage display to Ndel1 obtained in titer check plates were picked from round 1 to 4 of panning and cultured in two 96 well plates. A Boekel replicator was used to subculture the clones for small-scale rescue and display while the remainder was made to 15% glycerol and stored frozen.

ELISA with phages or purified nanobodies

ELISA was performed using high binding 96-well plates coated with 100 μl per well of 1 μg/ml of MBP-Ndel1, MBP-Lis1 or BSA in PBS overnight at 4^o C. The coated plates were washed three times with PBS and blocked with 2% skim milk in PBS for 1 h. Polyclonal or monoclonal phage solutions diluted with 2% milk in PBS were added to the plates for 1 h, then washed in PBS-T and PBS (3 times each). After the washes, anti-M13 phage antibody conjugated with HRP (GE Healthcare) at the dilution of 1/5000 with 2% milk in PBS was added to the plate and incubated for 1 h. The washing was repeated, followed by adding 1-Step Ultra TMB-ELISA substrate solution (Thermo Fisher). When signals appeared, 2.5 M sulfuric acid was added to the plates to stop the color reaction. ELISA signals were measured as absorbance ratio 450 nm/ 405 nm in a microplate reader (BioRad model 680).

For ELISA with purified nanobodies, 96 well plate was coated with 1 μg/ml Ndel1-MBP or BSA and blocked as described above. Purified nanobodies as described below were diluted in 2% skim milk in PBS/0.05% Tween-20 at 2 μg/ml and incubated on the coated plate for 4 h at room temperature. After washes with PBS-T, mouse anti-His-tag antibody (1/2000, GeneTex) was added for 1 h at room temperature. The plate was incubated with anti-mouse IgG conjugated with horseradish peroxidase (1/2000, Jackson Immunoresearch) for 1 h. After washes with PBS-T, 1 mg/ml OPD in a solution of 0.1 M citric acid, 0.2 M Na₂HPO₄, pH 5, 1 μl/ml H₂O₂ was added (140 μl per well) and incubated until color reaction developed. 100 μl of concentrated HCl was added to each well to stop the reaction.

Nanobody production and purification

Pools or monoclonal colonies harboring pecan126 phagemid clones were cultured in 3–5 ml LB media containing 50 μg/ml Amp until the culture reached OD₆₀₀ = 0.4–0.6. Protein production was induced by adding 0.5 to 1 mM IPTG and cultured for 5–6 h at 37^o C or overnight at 30^o C. After centrifugation at 13,000 rpm for 2 min, pellets were dissolved in 100 μl of TES buffer (0.1 M Tris-HCl, pH 8.0, 1 mM EDTA, 500 mM sucrose and 1 mM PMSF) and kept on ice for at least 30 min. For osmotic shock, 150 μl of cold 0.2 x TES buffer was added for at least another 30 minutes. Periplasm containing nanobodies was collected in the supernatant after centrifugation at 13000 rpm for 20 min, and NaCl was added to 300 mM final concentration and the extract stored at 4 ^oC. These periplasm preparations were used for immunostaining and immunoblotting as described below.

12 clones on 96 well plate containing monoclonal bacteria obtained through phage display to Ndel1 were chosen based on positive ELISA signals and cultured in LB +100 μg/ml Amp. After boiling preps of pecan21 plasmids containing nanobody cDNA, DNA sequencing was performed, which revealed that 12 clones were classified into 5 groups. Five plasmids with distinct sequences were digested with Sfi I and subcloned into Sfi I digested pecan16 vector that encodes His⁶ tagged alkaline phosphatase at the C-terminus [27]. Plasmid DNA was isolated and re-transformed into BL21Star cells and plated. The obtained colonies were cultured in 3 ml of LB + Amp at 37° C until cultures reached the OD of 0.47–0.69. IPTG was added at the concentration of 1 mM to induce protein expression overnight at 30° C. Periplasm was prepared from the culture as described above.

Monoclonal nanobodies were purified from periplasm obtained from 100–500 ml culture through Ni-ion affinity chromatography using His60-Ni-Superflow resin (Clontech) according to the manufacturer’s instructions. Monoclonal nanobodies were eluted from the resin with 50 or 250 μl of 250 mM imidazole buffer (pH 8.0) five times. Total protein level was measured at OD₅₉₅ nm with BioRad protein assay using BSA as standard. The eluates were either dialyzed with PBS or frozen after adding glycerol to 50% and used for immunostaining, immunoblotting and immunoprecipitation as described below.

Mammalian cell transfection

HEK293T cells (ATCC) were cultured in Dulbecco’s modified Eagle’s medium (DMEM-GIBCO) supplemented with 10% fetal bovine serum (Gemini-Bioscience), when semiconfluent, were transfected with plasmids using linear polyethylenimine (MW 25,000; Polysciences) as described [28]. Briefly, Sport6-Ndel1 DNA (Dharmacon) was diluted in serum free DMEM at 1 μg/μl and mixed with polyethylenimine (1 mg/ml in H₂O) at 3:1 ratio, the transfection mix was added to the cells for 6 h. The cells were washed with PBS, cultured in serum-containing DMEM for 48 h, then lysed in 1% Triton X100, 50 mM NaCl, 1 mM EDTA, 10 mM Tris HCl (pH 7.5) containing protease inhibitor cocktail (Roche) for protein analysis.

Identification of Npm2 as the antigen recognized by several nanobodies

To identify the nuclear antigen bound by NbG12, we decided to use reverse proteomics. Pulldown of endogenous antigens using NbG12 revealed a prominent Coomassie blue-stained 170 kDa band that corresponds to the band recognized with nuclei-specific nanobodies (Fig 4A, compare with Fig 3D). This band was absent when the pulldown was carried out with NbT15, a nanobody staining perinuclear structures (Fig 4A).

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Fig 4

Identification of Npm2 as an antigen recognized by NbG12.

(A) Reverse proteomics approach to identify the antigen recognized by NbG12. Lysates from 50 gastrula embryos were precipitated with 7 μg of NbG12 or NbT15 and 25 μl of Ni ion resin and separated by SDS-PAGE. After Simply Blue staining, 170 kDa protein band that was precipitated with NbG12 and the corresponding gel area from NbT15 pulldown were excised for LC-MS/MS analysis. (B) Top hits from the LC-MS/MS analysis of the 170 kDa band. Npm2 is detected with high abundance in NbG12 but not in NbT15 pulldowns.

The 170 kDa band was cut out from the gel and subjected to LC-MS/MS analysis. Among top-scored proteins with significant peptide coverage in the experimental but not control fraction was the histone-binding chaperone Npm2 or nucleoplasmin [31–33](Fig 4B). We conclude that Npm2 is the antigen recognized by NbG12 and likely by seven other nanobodies reacting with a band of similar mobility. Although Npm2 has a predicted molecular weight of 22 kDa, it is known to form stable decamer complexes that migrate around 170–180 kDa in SDS-PAGE [34]. We propose that NbG12 recognizes a conformational antigenic determinant that is specific for the Npm2 oligomer rather than the monomer. Alternatively, Npm2 oligomers may represent the preferred state of Npm2 in embryonic cells. The Npm2 determinant appears to be highly immunogenic, because we isolated eight independent nanobodies that stain nuclei on embryo sections and detect a protein band of the same size on immunoblots.

Isolation of Ndel1-specific nanobodies using a non-immune semi-synthetic llama nanobody library

Because a limited range of nanobodies was identified in the immune llama library, the immune response may have been directed to a few strong immunogens present in Xenopus homogenates. We therefore decided to take an alternative approach and used a semi-synthetic non-immune llama nanobody library in pecan21 [25]. As a proof-of-principle, we carried out phage panning on wells coated with two highly purified Xenopus antigens Ndel1-MBP and LIS1-MBP [35] [36] [37]. To eliminate anti-MBP binders, the library was preincubated with LIS1-MBP or Ndel1-MBP before applying to wells coated with Ndel1-MBP or LIS1-MBP, respectively. After four rounds of panning and elution, polyclonal phages were tested in ELISA on plates coated with respective antigens. Positive reactivity was observed for Ndel1-MBP-coated wells with virtually no cross-reactivity to LIS1-MBP or BSA. Sequencing revealed five groups of phages with distinct complementarity-determining regions (CDR) that are involved in Ndel1 binding, from which five unique clones were chosen for further analysis (Fig 5A).

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Fig 5

Isolation of Ndel1-specific nanobodies.

(A) amino acid sequence alignment of six nanobodies. Orange boxes indicate the two conserved cysteine residues, and blue boxes indicate the three complementarity-determining regions (CDRs). (B) wells coated with purified Ndel1-MBP protein (1 μg/ml) are positive in ELISA after probing with several Ndel1-specific nanobodies but not with negative controls (no Nb Co or NbN39). Control BSA coating confirms specificity. (C) immunoblotting of Xenopus Ndel1. Lysates from xNdel1-transfected or control (-) HEK293T cells were separated by SDS-PAGE and visualized with 2 μg/ml of purified AP-NbE7 and AP substrate. Purified Ndel1-MBP, but not LIS1-MBP is detected with NbE7. ERK1/2 antibody controls loading. (D, E) Ndel1 is precipitated by NbE9 from transfected cell lysates (D) and injected Xenopus embryos (E). (D) HEK293T cells were transfected with Xenopus Ndel1 plasmid as indicated. Cells were lysed after 24–48 h culture. Pulldowns were carried out with 2 μg of 6His-AP-NbE9 (asterisk) and 20 μl of Ni-agarose beads. (E) four-cell embryos were injected with 100 pg of xNdel1 DNA. The injected embryos were lysed at stage 38 and the pulldown was performed as in D. Arrows in D, E, indicate the 39 kD band corresponding to xNdel1. AP-NbE9 and AP substrate were used in immunoblotting for signal detection (D, E).

Detection of Ndel1 protein in mammalian cells and Xenopus embryos

The selected inserts from the positive monoclonal phages were subcloned into pecan16 to generate His⁶-tagged alkaline phosphatase protein fusions [27]. The nanobodies were purified from periplasmic extracts using IMAC and used for ELISA and immunoblotting. ELISA confirmed specificity for 5 different antibodies (NbE9, NbE7, NbE2, NbG6, NbH3, Fig 5B) that bound Ndel1 but did not react with BSA (negative control). By contrast, NbN39 that is specific for Npm2 did not bind Ndel1.

We next assessed whether the nanobodies can detect Ndel1 after immunoblotting. HEK293T cells were transfected with a plasmid encoding Xenopus Ndel1. NbE7 strongly reacted with purified Ndel1-MBP mixed into the untransfected cell lysate, whereas LIS1-MBP was undetectable in these conditions (Fig 5C). Moreover, a sharp band of the predicted size (39 kDa) appeared in cells transfected with Xenopus Ndel1 plasmid (Fig 5C). Collectively, these results demonstrate that NbE7 can detect denatured Ndel1 protein.

To address whether NbE9 can immunoprecipitate Ndel1 protein from cultured mammalian cells, the lysates of HEK293T cells transfected with Xenopus Ndel1 expression plasmid were incubated with NbE9 and Ni affinity resin. We found that NbE9 pulled down transfected Xenopus Ndel1 (Fig 5D, arrow). Similarly, embryos injected at the 4-cell stage with 100 pg of a plasmid containing Xenopus Ndel1 cDNA were lysed at stage 38 and the pulldown was done with NbE9 and Ni agarose beads overnight. E9 pulled down injected Xenopus Ndel1 from embryo lysates (Fig 5E, arrow). These results demonstrate that purified nanobodies can precipitate Xenopus Ndel1 from transfected cells and injected embryos.

We acknowledge the help of Sonya Li who participated in the early stages of this project. We thank Viki Allan for purified Ndel1-MBP and Lis1-MBP, and many other Xenopus investigators for their support and encouragement.