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Nanobody against NPR-C for growth disorder

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75N98026Q01031Federal

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Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

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This project focuses on the development of high-affinity and specific VHH nanobodies against human NPR-C to create potential therapeutics for growth disorders like achondroplasia. The scope of work involves two possible development tracks: phage/yeast display using immunized libraries or single B-cell cloning. The process includes antigen generation, alpaca or llama immunization, library construction or B-cell isolation, and rigorous screening and sequencing to identify unique clones. The final goal is to produce and characterize at least 10 unique VHH-Fc candidates with a target affinity of KD=10nM or better, ensuring no cross-reactivity with NPR-B. The project is expected to be completed within four to six months, with deliverables including serum titer reports, sequence data, purified antibodies, and a final summary report. The NIH retains all intellectual property ownership of the resulting antibodies and data. Out of scope activities include humanization, affinity maturation, GMP manufacturing, and stable cell line development. The contract follows a milestone-based payout structure and requires vendors to comply with IACUC-equivalent animal welfare standards.

General Info

Develop high-affinity VHH nanobodies against human NPR-C for growth disorder therapeutics.

Agency

Department Of Health And Human Services → National Institutes Of Health OlaoView Agency

NAICS

541714 - Research and Development in Biotechnology (except Nanobiotechnology)View NAICS

Place of Performance

Bethesda, MD, 20892, USA

Set-Aside

SBA

Documents

(1)

STATEMENT+OF+WORK+%28SOW%29.pdf

PDF

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Organization & Contact Information

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AgencyDepartment Of Health And Human Services → National Institutes Of Health Olao
Contacts1 person available
OfficeBETHESDA, MD, 20892, USA
Organization / Agency
Department Of Health And Human Services → National Institutes Of Health Olao
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Office AddressBETHESDA, MD, 20892, USA
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Full Description

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See attached Word document.


Project Title: Nanobody against NPR-C for growth disorder 


1. Project Overview 


1.1 Background 


We sought to develop nanobodies (VHH) against human NPR-C with high affinity and specificity for future clinical use. These nanobodies could potentially be further developed into therapeutics for treatment of growth disorders such as achondroplasia.  


1.2 Main Objectives 


- generation of antigens needed for immunization 


- immunization of Alpaca/Ilama with target antigens generated 


- generation of immunized phage/yeast library and in vitro screening using the library 


- alternatively, single B-cell screening and sequencing instead of phage/yeast library generation/screening. 


- downstream functional confirmation of VHH nanobodies binding to target antigens 


- generation of final VHH-Fc candidates for further validation 


1.3 Intended Use of Antibodies 


  • Research (Western blot, immunohistochemistry, ELISA) 


  • Animal testing (subcutaneous injection in mice) 


  • Therapeutic lead generation (in combination with other antibody domains, Fc, etc) 



2. Target / Antigen Information 


Field 


Detail 


Target name/ID 


Human NPR-C (P17342 · ANPRC_HUMAN) 


Species reactivity required 


Human / Mouse / Rat / Cross-reactive 


Target type 


secreted / extracellular domain 


Antigens to be provided (amount needed: 0.5-2mg) 


  1. Human NPR-C, Fc tag (immunization) 


  1. Human NPR-C, His tag (immunization) 


  1. Biotinylated human NPR-C, His tag (panning) 


  1. Mouse NPR-C, His tag (immunization) 


  1. Human NPR2, mFc tag (counter screening) 


  1. Human IgG1 Fc Protein, His-Avi Tag (counter screening) 


  1. Human CNP (blocking screening) 


Known structural considerations 


Avoid cross-reactivity with Alpaca/Llama NPR-C and NPR-B 



3. Scope of Work 


  1. Development Platform  


  • Track 1: Phage display or Yeast display using immunized library 


  • Track 2: Single B-cell cloning 


3.2.1 Workstream Breakdown for Track 1 (phage/yeast display) 


Phase 1 — Antigen Generation (less than 1 month) 


  • Antigens listed in section 2 to be generated and validated for purity before proceeding to immunization. 


Phase 2 — Immunization / Library Generation (1-2 months) 


  • 1-2 naïve Alpaca/Llama to be immunized. 


  • Alpaca/Llama shall be immunized four times with antigen over six to eight weeks. Up to two extra boosts shall be performed (preferably at no cost) if the serum titer is below the level required (1:15000) for phage display library construction. 


  • Anti-serum titer to be performed with ELISA against human and mouse NPR-C-His 


  • Peripheral blood mononuclear cell (PBMC) to be collected for library construction after immunization and confirmed serum titer 


Phase 3 — Library Construction (up to 1 month) 


  • PBMC collected will be used for library construction 


  • VHH genes to be PCR amplified and cloned into phage or yeast display vector for library construction 


  • A phage/yeast display library with a size of 1x108 or greater is required to proceed to the next step 


  • 50 colonies shall be selected by random to check for insertion, an insertion rate of 95% or greater, and a diversity of 90% or greater, is required to proceed to screening 


Phase 4 — Screening and Sequencing (1-2 months) 


  • 3 rounds of screening for human NPR-C are required 


  • Counter screening should be performed against human NPR-B 


  • Counter-screening (e.g., against homologous proteins, for specificity) 


  • Individual phage clones shall be confirmed using phage ELISA against human and mouse NPR-C 


  • Background ELISA screenings shall be carried out with Human Fc 


  • Positive clones will be sequenced, and sequence diversity analysis shall be performed. 


  • Expected number of positive clones: 20-100 unique clones  


Phase 5 — Expression and Purification (less than 1 month) 


  • At least 10 confirmed binders chosen based on sequencing and ELISA shall be produced with human Fc tag (hereafter VHH-Fc) in CHO/Expi293, or comparable mammalian cells. 


  • VHH-Fc shall be purified through Protein A affinity chromatography. SDS-PAGE and SEC-HPLC shall be used as QC for purification. Purified samples are subject to further characterization  


Phase 6 — VHH-Fc characterization (less than 1 month) 


  • ELISA shall be performed to confirm dose-dependent binding activity of purified VHH-Fc hits to human and mouse NPR-C protein. 


  • Counter screening to NPR-B by dose-curve ELISA shall be performed. 


  • Ability of VHH-Fc to block CNP binding to NPR-C shall be performed by dose-dependent ELISA blocking assay. 


  • SPR shall be used to evaluate the binding affinity of VHH-Fc to human NPR-C-His 


  • Full KD detection of selected VHH-human Fc antibodies via Biacore (or comparable).  


Phase 7 — Project Completion (total expected time: 4-6 months) 


  • At least 10 (ten) unique sequences of VHH antibodies, purified antibodies (1mg/antibody) and plasmids.  


  • A unique sequence is defined as one that has at least 1 unique amino acid in the three CDR regions relative to the sequences of the other clones. 


  • Final project report (sequence report, affinity, ELISA binding results, etc) 


3.2.2 Workstream Breakdown for Track 2 (Single B-cell cloning) 


Phase 1 — Antigen Generation (less than 1 month) 


  • Identical to track 1 


Phase 2 — Immunization (1-2 months) 


  • Identical to track 1 


Phase 3 — Single B-Cell Isolation and Screening (up to 1-2 months) 


  • Antigen-specific B cells shall be isolated from PBMCs/lymphoid tissue via fluorescence-activated cell sorting (FACS) using labeled human NPR-C antigen as bait, or an equivalent single-cell isolation method proposed by the vendor. 


  • Vendor shall report total B cells screened and number of antigen-specific single cells recovered. 


  • Counter-screening against human NPR-B shall be performed at the single-cell stage where the vendor's platform allows, to minimize downstream cross-reactive candidates. 


  • At least 100 antigen-specific single cells are expected to be carried forward for sequencing 


Phase 4 — Sequence Recovery and Analysis (up to 1 month) 


  • VHH variable region genes shall be recovered from each confirmed antigen-specific single cell via RT-PCR and sequenced. 


  • Sequence diversity analysis shall be performed to identify unique clones (per the uniqueness definition in Phase 7). 


  • Sequence liability screening (e.g., deamidation, glycosylation, unpaired cysteines) shall be reported for candidate sequences. 


Phase 5 — Expression and Purification (less than 1 month) 


  • Identical to Track 1 


Phase 6 — VHH-Fc Characterization (less than 1 month) 


  • Identical to Track 1 


Phase 7 — Project Completion (total expected time: 4-6 months) 


  • Identical to Track 1 


3.3 Explicitly Out of Scope 


The following activities are not included in this SOW. Vendors should not include costs for these items in their base proposal but may list them as optional add-ons with separate pricing if desired: 


  • Humanization or affinity maturation of VHH candidates 


  • Bispecific or multi-domain antibody engineering (e.g., fusion to additional Fc domains or antibody formats beyond VHH-Fc)  


  • GMP or GMP-like manufacturing of any antibody material 


  • Cell line development for stable production (beyond transient expression for characterization) 



4. Deliverables 



Deliverable 


Format 


Acceptance Criteria 



Serum titer report 


PDF/Excel 


titer curves, EC50 values, etc 



Sequence report 


PDF + FASTA 


VHH sequences, annotated CDRs, etc 



Purified antibody 


1 mg, liquid/lyophilized 


Purity ≥95% by SEC, endotoxin <5 EU/mg 


Expected affinity for human NPR-C: KD=10nM, or better 



Characterization data 


PDF/Excel 


ELISA, SPR, Biacore data, etc 



Final summary report 


PDF 


Recommendation of 10 lead candidates with data supported rationale 



5. Timeline 


Milestone 


Target Completion 


Phase 1: Antigen Generation 


2-4 weeks 


Phase 2: Alpaca Immunization 


6-8 weeks 


Phase 3: 


Library Generation (track 1), or 


Single B-Cell Screening (track 2) 



2-3 weeks (track 1)  


4-6 weeks (track 2) 


Phase 4: 


Phage Library Screening (track 1), or 


Single B-Cell Sequencing (track 2) 



4-6 weeks(track 1)  


2-3 weeks (track 2) 


Phase 5: VHH-Fc Production 


2 weeks 


Phase 6: Candidate Characterization 


2 weeks 


Project Completion: 


Total expected time: 4-6 months 



6. Materials and Responsibilities 


6.1 Provided by Client 


  • Reference antibodies, if needed. 


6.2 Provided by Vendor 


  • Animals, reagents, equipment, protocol 


6.3 Intellectual Property 


  • The NIH retains all IP ownership of resulting antibodies, sequences, and data. 



7. Quality and Compliance Requirements 


  • Animal work must comply with IACUC-equivalent standards; vendor to provide accreditation (e.g., AAALAC) 


  • Data traceability / lab notebook standards 


  • Certificate of Analysis (CoA) required for final deliverables 



8. Pricing Structure Requested 


Phase 


Description 


Payout 


Total Payout 


Phase 1 


Antigen Generation 


10% 


10% 


Phase 2 


Alpaca Immunization 


20% 


30% 


Phase 3 


Phage Library Generation / Single B-Cell Screening 


20% 


50% 


Phase 4 


Phage Library Screening / 


Single B-Cell Sequencing  


25% 


75% 


Phase 5 


VHH-Fc Production 


5% 


80% 


Phase 6 


Candidate Characterization 


10% 


90% 


Phase 7 


Project Completion 


10% 


100% 



9. Evaluation Criteria 


Criterion 


Weight 


Technical approach and platform justification 


40% 


Timeline 


20% 


Price 


20% 


Relevant experience / past performance with similar targets 


15% 


Quality certifications 


5% 



10. Proposal Submission Requirements 


Vendor response should include: 


  • Project proposal detailing approach narrative (platform choice, screening strategy, risk mitigation for difficult targets, etc) 


  • Proof of Team qualifications / expertise  


  • Detailed timeline with milestones 


  • Itemized pricing 


  • Quality/compliance certifications (if applicable) 



Submission format: PDF or microsoft word 


Submission method: Email 


Q&A Deadline: 8/24/2026 


Deadline:  8/28/2026

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