Special NoticePosted Sep 8, 2026·Responses due Dec 9, 2026

TIDAL: Target-Induced Droplet Assembly of Ligands

Energy · TRIAD - DOE CONTRACTOR

Stage
Early notice (sources sought, presolicitation or special notice)
NAICS
541714
Value
Not stated
Solicitation
S-197478
Set-aside
No Set aside used
PSC
AJ11
Place
Los Alamos, NM, USA
Contact
Caleb Ledgerwood (licensing@lanl.gov)
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Where this opportunity stands

Every notice posted under solicitation S-197478 in this department, oldest first.

Early notice
  • Sep 8, 2026 · this notice
    Special Notice
Solicitation
None posted
Award
Not yet. Typical award: Sep 29, 2026 to Nov 29, 2026, middle of the range Oct 9, 2026.
Measured from 192 past early notices at Energy, Department of that later posted an award (middle half of cases, counted from Sep 8, 2026).
Responses are due Dec 9, 2026, so an award before then is unlikely; past cases include short solicitations.

Next steps for this stage

Standard steps for the notice type; not advice about this buyer.

  • Answer the notice: this is when the requirement can still be shaped.
  • Contact the contracting officer named on the notice.
  • Check who won similar work; they are the likely bidders.

What the notice says

Developed by Los Alamos National Laboratory, TIDAL (Target-Induced Droplet Assembly of Ligands) transforms the small antibody fragments known as nanobodies into a programmable, protein-only material that organizes itself on demand. By harnessing a natural process called liquid-liquid phase separation, TIDAL lets these binders gather into dense, dynamic droplets precisely when they encounter their intended target, giving developers a single platform that can purify proteins without costly resins, deliver drugs as a self-forming slow-release depot and even trap harmful proteins inside living cel… (show all)

ls. The outcome is a versatile toolkit that lowers production costs, simplifies manufacturing and opens fresh therapeutic and diagnostic possibilities, all from a building block that biology already knows how to make. Overview At the heart of TIDAL is a small, engineered tag, called an encapsulation peptide (EP), that is fused to a nanobody. When many of these tagged nanobodies are present, they undergo liquid-liquid phase separation, similar to what makes oil bead up in water, and they collect into concentrated liquid droplets made entirely of protein. Binding to the target molecule intensifies the effect, so the droplets form most strongly exactly where and when that target is present. Because the assembly is dynamic and reversible, the droplets behave as stimuli-responsive materials whose thickness and flow can be tuned by the target ligand, allowing one design to serve as a purification handle, a delivery vehicle or an intracellular trap. Technology Description TIDAL: Target-Induced Droplet Assembly of Ligands treats the nanobody itself as a structural component rather than merely a binding reagent. Each fusion polypeptide pairs a target-specific nanobody with the encapsulation peptide (EP), and it is the peptide that drives the many weak, cooperative interactions responsible for phase separation. In solution these interactions produce biomolecular condensates, dense droplet phases that concentrate the nanobodies far above their ordinary levels; the presence of the matching ligand pushes the balance further toward condensation. Because condensation is governed by many cooperative contacts rather than a single rigid bond, the droplets stay liquid-like and dynamic, and their formation can be reversed when the trigger is removed. Building on that behavior, the droplets function as programmable modules for delivery, stability or signal enhancement. Their rheology, meaning how readily they flow, can be switched by the target ligand, so a preparation can remain fluid enough to pass through a fine needle yet convert into a slow-release depot once injected. The same concentrating power lets the droplets scavenge and enrich internalized components to levels far above normal, which sharpens detection in diagnostics, and, when produced inside cells, the condensates can sequester disease-driving proteins such as oncogenic or viral factors into synthetic granules that block their activity. Purification follows the same logic: Triggering condensation precipitates the bound target out of solution, offering a resin-free alternative to the slow and expensive column methods used today. Advantages Cuts protein purification costs by replacing slow, expensive column resins with a simple trigger-and-precipitate step Enables patient-friendly, at-home injections that stay liquid in the syringe then set into a slow-release depot Works entirely from protein, avoiding synthetic carriers and easing manufacturing Can operate inside living cells to trap and neutralize harmful proteins linked to cancer or viral infection Boosts diagnostic sensitivity by concentrating faint signals into detectable droplets Offers one adaptable platform spanning manufacturing, therapy and detection Market Applications � Biopharmaceutical Manufacturing (antibody and enzyme purification, protein production) � Therapeutics and Drug Delivery (subcutaneous slow-release treatments, intracellular protein targeting) � Diagnostics (high-sensitivity detection assays, point-of-care testing) � Biotechnology (resin-free enzyme immobilization, biocatalysis) � Reagents (protein capture, condensate-based cell studies) TRL 3 U.S. Patent pending LA-UR-26-27937 LANL Tech Partnerships: Unlock the Innovative Potential Los Alamos National Laboratory offers a wide range of cutting-edge technologies and capabilities that may provide your company with a competitive edge in the market and unlock the innovative potential that can enhance, refine, and revolutionize your products. LANL�s licensing program focuses on moving inventions developed by our researchers to commercial innovations. Patented and patent pending inventions and copyrighted software are available to existing and start-up companies through exclusive and non-exclusive licensing agreements. For specific discussions, please contact licensing@lanl.gov. Note: This is not a call for external services for the development of this technology. https://www.lanl.gov/engage/collaboration/feynman-center/partner-with-us/licensing-technology m.lanl.gov/tech-search

Who won similar work

834 award notices on SAM.gov in the last 24 months. Matched by: Same agency (Energy), any industry: a loose match.

Loose match: same agency, any industry. Read the titles before treating these as competitors.

Single-winner award sizes (819): middle half $28K to $497K, median $85K; range $267 to $3.0B.

WinnerAwardsValueLast
DH TECHNOLOGIES, INC.16$2.8MSep 29, 2026
VALI COOPER INTERNATIONAL LLC14$37.2MAug 5, 2026
ENERGY BY NATIVE AMERICAN DESIGN CORP11$2.8MJun 2, 2026
RLH INC.11$514KSep 2, 2026
COUNTERTRADE PRODUCTS, INC.11$300KSep 24, 2026
THUNDERCAT TECHNOLOGY, LLC9$3.4MAug 13, 2026
VECTOR RESOURCE INC8$85.9MAug 3, 2026
HUGHES BROTHERS INC8$10.3MAug 20, 2026
Aantilia LLC8$504KSep 24, 2026
SOFTWARE INFORMATION RESOURCE CORP.8$82KJul 27, 2026

Value counts single-winner awards. "Shared" awards are multiple-award contracts that list every winner with the same total ceiling; that ceiling is not one company's win, so it is not added in. Revenue next to a ticker is the company's last annual revenue from its 10-K.

Latest awards

Materiality: one award's value as a share of the winner's revenue over the latest 12 months in its SEC filings (or its last fiscal year, as noted when you point at it). Low under 1%, Medium 1 to 5%, High 5% or more. Many awards are paid over several years, so this overstates a single year's share.

Competitive landscape

For the 8 most frequent past winners above. Lobbying is matched by the company's exact name or exact ticker; agencies are as named on the filings.

  • 0 of these past winners lobbied Energy, Dept of since 2024 (0 filings)
  • 0 of their lobbyists list a past Energy, Dept of job
  • No corporate PAC money from them to the overseeing committees since 2024
  • 0 foreign-agent (FARA) registrations
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Policy around it

Bills the past winners named while lobbying this agency's issues, rules from the department, and executive orders that name the agency, last 12 months.

  • 0 bills named on the past winners' lobbying filings
  • 75 rules from the department in the last 12 months
  • 0 executive orders naming the agency in the last 12 months
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Market

For past winners matched exactly to a listed company. Insider trades are open-market buys and sells (Form 4) in the last 90 days, shown as facts; our own study found insiders do not reliably buy ahead of awards. A sale marked 10b5-1 was made under a trading plan set up in advance.

  • 0 of the past winners are listed companies
  • 0 insider buys and 0 insider sells at them in the last 90 days
See who and the source records with Pro

Sources: SAM.gov notices and award notices; Senate LDA lobbying filings; FEC filings; FARA; Federal Register; congress.gov; SEC Form 4. Every row above links to its record.

Companies are matched to tickers by exact name only. A company we could not match shows no market rows; that is a miss, not a finding.