Case Summary:          

We are pleased to share the success story of an EB‑1A petition approval granted to a medicinal chemistry postdoctoral fellow from Pakistan whose work spans structure‑based drug design/discovery, ligand‑protein interaction modeling, phenotypic and virtual screening, and CRISPR/Cas12‑based diagnostic innovations. At the time of filing, the client held a research scientist position at a U.S. medical research institution and had built a substantial record of high-impact scholarship and service.

Research Focus and Contributions:
The petition highlighted the client’s multifaceted research program, which includes:

• Designing and optimizing small‑molecule inhibitors targeting cancer and infectious disease pathways, using structure‑guided biochemical assays to validate binding and mechanism
• Modeling ligand–protein interactions through computational simulations to accelerate hit‑to‑lead progression and elucidate the mechanism of action
• Developing CRISPR/Cas12‑mediated lateral‑flow biosensors for rapid, point‑of‑care detection of viral and bacterial nucleic acids

Research Impact and Scientific Contributions:
To demonstrate extraordinary ability, the petition assembled evidence across key metrics:

• 34 peer‑reviewed journal articles, 5 conference abstracts, and 2 book chapters in leading venues such as Cell Chemical Biology, iScience, Expert Opinion on Therapeutic Targets, Cancer Letters, Biosensors and Bioelectronics, Bioorganic Chemistry, Pharmacological Research, and Advances in Experimental Medicine and Biology
• 1,306 citations, placing the client in the top 1 percent most‑cited authors in medicinal chemistry (h‑index 17)
• Peer Review & Editorial Service: Conducted over 25 manuscript reviews for high‑impact journals and served on editorial boards, underscoring recognition as an authority in the field

These quantitative indicators, together with evidence of the commercialization of key compounds, confirmed major significance and broad influence.

Here is a compelling excerpt from one of the recommendation letters that highlights how the client’s research benefits the United States:

“[Client] identified a compound that inhibits Skp1’s interactions with partner proteins, disrupting its normal function. This led to the conclusion that disrupting these interactions promotes cell death via activation of the p53 protein, highlighting a new avenue for developing novel cancer therapies.”

Well Positioned to Advance Extraordinary Research:
We emphasized the client’s advanced degree training (Ph.D. in medicinal chemistry), rigorous postdoctoral experience, and current role at a top U.S. institution conducting biochemical studies on ubiquitin‑mediated regulation and targeted protein degradation. Letters from independent experts further corroborated the client’s status as one of the leading scientists driving innovations in drug discovery and diagnostic technologies.

Approval and Outcome:
Filed November 8, 2024, and approved February 7, 2025, in just 2 months and 30 days, the EB‑1A petition affirms the national interest in securing this researcher’s extraordinary contributions. NAILG is proud to have guided this client through a successful EB‑1A process and looks forward to supporting ongoing advancements in medicinal chemistry and global health diagnostics.