Describing inhibitor specificity for the amino acid transporter LAT1 from metainference simulations
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Abstract
The human L-type amino acid transporter 1 (LAT1; SLC7A5) is a membrane transporter of amino acids, thyroid hormones, and drugs such as the Parkinson's disease drug levodopa (L-Dopa). LAT1 is found in the blood-brain barrier, testis, bone marrow, and placenta, and its dysregulation has been associated with various neurological diseases, such as autism and epilepsy, as well as cancer. In this study, we combine metainference molecular dynamics simulations, molecular docking, and experimental testing, to characterize LAT1-inhibitor interactions. We first conducted a series of molecular docking experiments to identify the most relevant interactions between LAT1's substrate-binding site and ligands, including both inhibitors and substrates. We then performed metainference molecular dynamics simulations using cryoelectron microscopy structures in different conformations of LAT1 with the electron density map as a spatial restraint, to explore the inherent heterogeneity in the structures. We analyzed the LAT1 substrate-binding site to map important LAT1-ligand interactions as well as newly described druggable pockets. Finally, this analysis guided the discovery of previously unknown LAT1 ligands using virtual screening and cellular uptake experiments. Our results improve our understanding of LAT1-inhibitor recognition, providing a framework for rational design of future lead compounds targeting this key drug target.
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l-DOPA is recognized by the large neutral amino acids transporter 1 on endothelial cells and transported across the blood-brain barrier for treatment of Parkinson's disease.
“Specifically, l-DOPA can be recognized by the large neutral amino acids transporter 1 on endothelial cells and be transported across the BBB for the treatment of Parkinson’s disease29–31.”
From Blood–brain-barrier-crossing lipid nanoparticles for mRNA delivery to the central nervous system (2025) · cites this paper as [31]
The Introduction (page not provided) states that LAT1 is abundant in blood-brain-barrier endothelial cells and mediates levodopa (L-DOPA) transport across the barrier. It does not state that this transport is for treatment of Parkinson’s disease; that treatment detail is not established by the eligible Introduction passages. (LLM, conf=0.78)
Experimental — accuracy not yet measuredd-Serine crosses the blood-brain barrier by amino acid transporter solute carrier family 6 member 14.
“d-Serine serves as a neuromodulator and crosses the BBB by amino acid transporter solute carrier family 6 member 14 (refs. 31–35).”
From Blood–brain-barrier-crossing lipid nanoparticles for mRNA delivery to the central nervous system (2025) · cites this paper as [31]
The Introduction (page not provided) identifies LAT1 as SLC7A5 and says it is abundant at the blood-brain barrier. Searches for d-serine and SLC6A14 found no passage addressing whether d-serine crosses the barrier through SLC6A14. (LLM, conf=0.76)
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Directory of useful decoys, enhanced (DUD-E): better ligands and decoys for better benchmarking.
Mysinger, M. M., Carchia, M., Irwin, J. J., & Shoichet, B. K. (2012) · Journal of Medicinal Chemistry · doi:10.1021/jm300687e · Cited by 2,412 · see citing works
Sampling alternative conformational states of transporters and receptors with AlphaFold2
del Alamo, D., Sala, D., Mchaourab, H. S., & Meiler, J. (2022) · eLife · doi:10.7554/elife.75751 · Cited by 511 · see citing works
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Cited by
Sorted by citations
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Wang, C., Xue, Y., Markovic, T., Li, H., Wang, S., Zhong, Y., Du, S., Zhang, Y., Hou, X., Yu, Y., et al. (2025) · Nature Materials · doi:10.1038/s41563-024-02114-5 · Cited by 171 · see citing works
- Authors
- Hutchinson, K., Silva, D. B., Bohlke, J., Clausen, C., Thomas, A. A., Bonomi, M., & Schlessinger, A.
- Affiliations
- Icahn School of Medicine at Mount Sinai (US)
- University of California, San Francisco (US)
- University of Nebraska at Kearney (US)
- Centre National de la Recherche Scientifique (FR)
- Corresponding author
- Bonomi, Massimiliano
- Schlessinger, Avner
- Venue
- Biophysical Journal
- Publisher
- Elsevier BV
- Published
- 2022-12
- Volume
- 121
- Issue
- 23
- Pages
- 4476-4491
- ISSN
- 0006-3495 (ISSN-L)
- PMC
- PMC9748366
- OpenAlex
- W4308804464
- Cited by
- 18
- References
- 2
- Citations by year
- 2026: 7 · 2025: 6 · 2024: 3 · 2023: 1 · 2022: 1
- FWCI
- 1.49
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Biophysical Journal (publishedVersion)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion, cc-by-nc-nd)
- Funders
- Icahn School of Medicine at Mount Sinai
- Agence Nationale de la Recherche (ANR-20-CE45-0002)
- NIH (R01 GM108911, R15 NS099981, T32 GM062754)
- Topics
- Physical Sciences › Computer Science › Computational Theory and Mathematics › Computational Drug Discovery Methods
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Structure and Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Amino Acid Enzymes and Metabolism
- Keywords
- LAT1, SLC7A5, amino acid transporters, inhibitor specificity, substrate binding site, cryo-EM structure, druggable pockets, virtual screening, cellular uptake, drug target design, Parkinson's disease, blood-brain barrier
- MeSH terms
- Humans, Cryoelectron Microscopy, Amino Acid Transport Systems, Molecular Docking Simulation
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