Affinity Labeling Detection of Endogenous Receptors from Zebrafish Embryos

Summary

A novel technique for the detection of low abundance endogenous receptors present in zebrafish embryos is described. We have named it AFLIP because it consists of affinity labeling of the receptor by its ligand linked to immunoprecipitation.

Abstract

By combining the powers of Affinity Labeling and Immunoprecipitation (AFLIP), a technique for the detection of low abundance receptors in zebrafish embryos has been implemented. This technique takes advantage of the selectivity and sensitivity conferred by affinity labeling of a given receptor by its ligand with the specificity of the immunoprecipitation. We have used AFLIP to detect the type III TGF-β receptor (TGFBR3), also know as betaglycan, during early zebrafish development. AFLIP was instrumental in validating the efficacy of a TGFBR3 morphant zebrafish phenotype. In the first step, embryo protein extracts are prepared and used to generate ¹²⁵I-TGF-β2-TGFBR3 complexes that are purified by immunoprecipitation. Later, these complexes are covalently cross-linked and revealed using SDS-PAGE separation and autoradiography detection. This technique requires the availability of a labeled ligand for, and a specific antibody against, the receptor to be detected, and shall be easily adapted to identify any growth factor or cytokine receptor that meets these requirements.

Introduction

Specific detection of proteins expressed during embryonic development is required to validate expression profiles obtained by measuring their cognate mRNAs with RT-PCR or in situ hybridization (ISH). This is commonly achieved by a western blot of embryo extracts followed by detection with specific antibodies. However, this approach is hard to apply to proteins that are in very low abundance, or that have properties that hamper their quantitative transfer during their blotting. Betaglycan, also known as the type III transforming growth factor β (TGF-β) receptor (TGFBR3), is an example of these difficulties. TGFBR3 is a part time membrane proteoglycan that binds TGF-β through its core protein¹, with notably higher affinity for the isoform TGF-β2, a property that distinguishes it from any other TGF-β binding protein². TGFBR3 in the zebrafish is expressed from 8 hpf on, reaching a maximum by 72 hpf, as detected by RT-PCR of its mRNA³.

However, despite the availability of a very specific antibody³, every attempt to detect its translated product by western blot proved unsuccessful. Reckoning that TGFBR3's proteoglycan nature, as well as putative low abundance may be accountable for this failure, a detection method, AFLIP, which takes advantage of TGFBR3 high affinity for TGF-β2 was devised. In this method a protein extract from pooled embryos is allowed to specifically bind ¹²⁵I-labeled TGF-β2 and the receptor-ligand complexes are purified by immunoprecipitation and cross-linked before separation by SDS-PAGE. The migration patterns observed by autoradiography of the gels revealed the presence and nature of the labeled receptor species. This approach combines the ligand specificity of affinity labeling with immunoprecipitation by specific antibodies, increasing detection range, avoiding the inefficient transfer blotting of TGFBR3. Due to its inherent properties, the AFLIP assay is not a quantitative assay but can be used to confidently gauge relative experimental differences in the analyzed receptor.

Protocol

All experiments carried out in animals were approved by the Committee for Laboratory Animal Care and Use of the Autonomous National University of México (UNAM), under the CICUAL-Protocol number: FLC40-14. (CICUAL: "Comité Institucional para el Cuidado y Uso de los Animales de Laboratorio del Instituto de Fisiologìa Celular, Universidad Nacional Autònoma de México").

1. Preparation of Embryo Protein Extract

1. Collect 100 - 200 embryos for each condition to compare (morphants vs. wild type) at desired stage, for example 72 hr post fertilization (hpf).
2. Place embryos in Petri dishes containing fish water (see Table 1) and manually dechorionate embryos using fine-tipped forceps. Avoid using pronase during this step (or any other protease throughout the protocol) as it may digest the targeted receptor.
3. Place embryos in a 1.5 ml microfuge tube and wash embryos twice with 1x phosphate buffer solution (PBS) (see Table 1).
4. Add 500 µl of deyolk buffer (see Table 1).
5. Release most of yolk by gently pipetting up and down (about 30 - 40 times) the embryos in the solution. For 72 hpf and 48 hpf embryos use blue and yellow pipette tips, respectively. Yellow tips may need to be slightly cut to avoid destroying embryos. The successful yolk release can be checked by observing embryos under microscope.
6. Collect embryos by centrifugation at 600 x g for 15 sec.
7. Discard supernatant carefully by using a pipet.
8. Wash embryos twice with 500 µl washing buffer (see Table 1) by gently vortexing at lowest speed.
9. Collect embryos by centrifugation at 600 x g for 15 sec.
10. Starting from here, continue the procedure at 4 °C.
11. Discard supernatant carefully by using a pipet.
12. Resuspend embryos in 350 µl of lysis buffer (see Table 1) and homogenize using a plastic pestle.
13. Incubate lysed embryos 30 min with agitation on a test tube rocker at 4 °C.
14. Centrifuge lysed embryos at 11,000 x g for 15 min in order to remove insoluble debris.
15. Transfer cleared supernatant using a pipet to a fresh tube.
16. Determine total protein by Bradford protein assay⁴, or other suitable procedure. If Bradford assay is used, perform the calibration curve in the presence of equivalent concentrations of the detergents presents in the lysis buffer, as they cause an underestimation of the protein standard⁴.

2. Detection of Endogenous Receptor Protein

1. Affinity Labeling and Immunoprecipitation (all these steps at 4 ^oC)
   1. Place 400 - 500 µg of total embryo protein in a 1.5 ml microfuge tube and dilute to 1 µg/µl with buffer 1 (see Table 1).
      Note: In order to obtain 500 µg of total embryo protein, about 100 - 200 embryos must be initially processed. 72 hpf embryos routinely yield ~ 5 µg of total embryo protein, which is sufficient for betaglycan detection.
   2. Add enough volume of labeled TGF-β2 stock to reach a final concentration of 150 pM and incubate with agitation on a test tube rocker 2 hr at 4 °C. TGF-β2 must be labeled before AFLIP is started, with ¹²⁵I by the chloramine T method as described by Cheifetz et al.⁵.
      CAUTION: Use shielding to minimize exposure while handling ¹²⁵I labeled ligand.
   3. Add enough volume of undiluted antibody against the receptor of interest in order to reach a 1:100 dilution and continue incubation for another 2 hr at 4 °C (incubation may be O/N). This is the optimal dilution of antiserum # 31, used in this study and described elsewhere³, but depending on the quality of the antibody, a larger or smaller dilution may be the optimal.
   4. Add 50 µl of suitable immunoglobulin binding beads (e.g., G-protein-Sepharose, which was previously equilibrated in TNTE and resuspended 1:5 of its original volume in TNTE) and incubate for 50 min with agitation on a test tube rocker at 4 °C.
   5. Recover the beads by microcentrifugation at 11,000 x g for 20 sec.
   6. Discard supernatant in an appropriate radioactive trash container.
   7. Wash the IP-beads three times with 1 ml of IP wash buffer (see Table 1), by vortexing and microcentrifugation at 11,000 x g for 20 sec each time.
   8. Resuspend IP-beads in 250 µl of IP wash buffer.
   9. Add 1.5 µl of disuccinimidyl suberate (DSS, dissolved in DMSO at 10 mg/ml). Prepare the DSS solution just before its use in this step.
   10. Incubate for 15 min at 4 °C with agitation.
   11. In order to quench the crosslinking reaction, add 500 µl of IP wash buffer, supplemented with enough Tris-Cl pH 7.4 stock to reach 25 mM Tris-Cl. The free amino groups in Tris capture unreacted DSS.
   12. Centrifuge at 11,000 x g for 20 sec to collect IP-beads and discard supernatant.
   13. Resuspend IP-beads in 30 µl of reducing Laemmli buffer.
   14. Boil samples 5 min at 94 °C.
   15. Optionally, analyze samples in a gamma counter using manufacturer's protocol.
2. Sample Analysis
   1. Subject samples to denaturing SDS-PAGE. Use polyacrylamide at the appropriate percentage for the mass of the receptor and run gel under standard procedure.
   2. Immerse gel in fixative solution (see Table 1) for 30 min at RT.
   3. Wash gel with distillated water for 15 min.
   4. Place gel in previously hydrated filter paper and cover with saran wrap film.
   5. Dry gel at 80 °C for 1 hr.
   6. Expose gel on a white phosphorimager screen at RT O/N.
   7. Scan exposed screen using a phosphorimager using manufacturer's protocol.

Results

Figure 1 shows a representative result obtained with AFLIP. Signals in Lane 1 come from the ¹²⁵I-ligand covalently linked to either the zebrafish betaglycan core protein (BG core, below the 150 kDa marker) or the BG core that has been processed to its proteoglycan form by attachment of glycosaminoglycans (GAG, smear ranging from 170 kDa to the top of the gel). This pattern of migration, a sharp core protein plus a smeared proteoglycan (due to heterogeneity in t...

Discussion

The use of Western blots with a specific antibody against a protein of interest is a valuable tool to study its expression⁷ during embryogenesis. However, immunoblotting of highly-glycosylated proteins has not been very successful due to their inefficient transfer and weak binding to nitrocellulose or PVDF membranes^8,9.

Proteoglycans are a good example of this shortcoming, because of their covalently attached glycosaminoglycan chains (GAG) that are negatively charged and ...

Materials

Name	Company	Catalog Number	Comments
Disuccinimidyl suberate (DSS)	ThermoFisher Scientific	21555
Protein G Sepharose 4 Fast Flow	GE Healthcare Life Sciences	17-0618-01
Gel Dryer Model 583	BIO-RAD	1651745
Typhoon 9400	GE Healthcare Life Sciences	63-0055-78
Cobra II Auto gamma counter	Packard
Exposure Cassette	Molecular Dynamics	63-0035-44
NaCl	J.T. Baker	3624
KCl	J.T. Baker	3040
Na2HPO4	J.T. Baker	3828
K2HPO4	J.T. Baker	3246
CH3OH	J.T. Baker	9070
CH3COOH	J.T. Baker	9508
HCHO	J.T. Baker	2106
SDS	Sigma-Aldrich	L4509
EDTA	Sigma-Aldrich	ED
Triton X-100	Sigma-Aldrich	T9284
CaCl2	Sigma-Aldrich	C3306
NaHCO3	Fisher Scientific	S233
PMSF	Sigma-Aldrich	P7626
Crystal Sea Marine Mix	Marine Enterprises International	http://www.meisalt.com/Crystal-Sea-Marinemix