Kaushki Sharma- BI3323

Classification: MEMBRANE PROTEIN

Organism(s): Homo sapiens

Expression System: Homo sapiens

Mutation(s): No

Deposited: 2024-11-13 Released: 2025-11-05

Deposition Author(s): Jeon, H.M., Eun, J., Kim, Y.

Funding Organization(s): National Research Foundation (NRF, Korea)

Experimental Data Snapshot

Method: ELECTRON MICROSCOPY

Resolution: 3.85 Å

Aggregation State: PARTICLE

Reconstruction Method: SINGLE PARTICLE

Introduction

Members of the organic anion transporter (OAT) family, including OAT1, are expressed on the epithelial membrane of the kidney, liver, brain, intestine, and placenta.^[2][3] OAT1 regulates the transport of organic anion drugs from the blood into kidney epithelial cells by utilizing the α-ketoglutarate (α-KG) gradient across the membrane established by the tricarboxylic acid (TCA) cycle.^{[4] [5]}OAT1 also plays a key role in excreting waste from organic drug metabolism and contributes significantly to drug-drug interactions and drug disposition. However, the structural basis of specific substrate and inhibitor transport by human OAT1 (hOAT1) has remained elusive. Here are four cryo-electron microscopy (cryo-EM) structures of hOAT1 in its inward-facing conformation: the apo form, the substrate (olmesartan)-bound form with different anions, and the inhibitor (probenecid)-bound form.

Cryo-EM structure of hOAT1

Fig 1. (A) Schematic diagram of human OAT1 topology and the overall transport process.

The apo state structure of human Organic Anion Transporter 1 (hOAT1), determined by cryo-EM, reveals the transporter in an inward-facing conformation. This means the central substrate-binding cavity is open toward the intracellular side of the membrane, ready to release a substrate or accept one from the cytoplasm.

Key Structural Characteristics:

• Overall Fold:

• Adopts the classic Major Facilitator Superfamily (MFS) fold.

• Comprises 12 transmembrane helices (TMs 1-12).

• Exhibits pseudo-two-fold symmetry, divided into an N-lobe (TMs 1-6) and a C-lobe (TMs 7-12).

• Central Binding Cavity:

• The cavity is located between the N-lobe (formed by TM1, TM2, TM4, TM5) and the C-lobe (formed by TM7, TM8, TM10, TM11).

• It possesses a positively charged electrostatic environment, which explains its strong preference for transporting anionic substrates.

• The cavity is lined by 29 residues, forming a hydrophobic and aromatic-rich environment.

• Cavity Borders and Cytosolic Gate:

• The top border (extracellular side) of the cavity is formed by residues including N35, Y230, Y353, and Y354 and are involved in substrate recognition

• The bottom border (cytosolic side) features a narrow "thin bottom gate" formed by residues M207 and F442. The interaction between these two residues splits the cytosolic entrance into two distinct pathways:

• Path A: Located between TM2 and TM11.

• Path B: Located between TM5 and TM8.

• This suggests that aromatic residues located at the top border are important for extracellular anion binding, while residues at the bottom play a role in exporting extracellular anions to the cytoplasmic side.

• Conformational State:

• In the apo state, the transporter is in a relaxed, inward-open conformation, providing access for substrates from the cytoplasm.

Olmesartan recognition by hOAT1

The structural and functional analysis of provides a detailed blueprint for substrate specificity and binding.

1. Binding Location and Pose

• Olmesartan binds within the central cavity of hOAT1 in an inward-facing conformation.

• It occupies Site 3 of the binding pocket, which is the primary polyspecific site for anionic substrates.

• The drug adopts a diagonal orientation relative to the membrane plane, a pose that requires more space than the smaller inhibitor probenecid. This orientation is similar to its conformation when bound to the angiotensin receptor.

2. Key Interacting Residues

• Olmesartan occupies Site 3 of the binding pocket and is located within 5A˚ distance of residues of TM1, TM4, TM5, TM7, TM10, and TM11, namely N35, M207, G227, Y230, W346, Y353, Y354, F438, F442, S462, and R466.

• The biphenyl group and tetrazole ring of olmesartan rely on interactions with hydrophobic residues close to the bottom gate in the binding pocket.

• Upon olmesartan binding, the side chain of Y230 undergoes a vertical rotation to accommodate and interact with the substrate.

• M207 and F442 residues forming the bottom gate of the binding pocket affect olmesartan interactions

Mechanism of OAT1 inhibition by probenecid

The cryo-EM structure of reveals a dual-mechanism of action that goes beyond simple competition, effectively arresting the transporter in a restricted state.

1. Binding Mode and Direct Competition

• Probenecid binds at the top of the central cavity, parallel to the membrane plane.

• Its binding site overlaps with both Site 1 (partially) and Site 3.

• In the binding pocket of Site 1, surrounded by 16 residues located within a 5 A ˚ (M31, N35, M142, V145, G227, Y230, W346, Y353, Y354, K382, D378, F438, S462, A465, R466, and S469).

• It engages in specific, high-affinity interactions with key residues:

• K382 on TM8 forms a hydrogen bond with the carboxylate group of probenecid.

• Y354 on TM7 forms a hydrogen bond with its sulfonyl group.

• Crucially, K382 is also the residue that interacts with the counter-substrate α-ketoglutarate (α-KG), establishing a direct competitive inhibition mechanism by blocking α-KG binding.

2. Conformational Arrest and Cytoplasmic Path Blockage

The primary inhibitory mechanism is a probenecid-induced conformational change that physically blocks substrate access and exit.

• Constriction of the Binding Pocket: Compared to the apo state, the cytoplasmic opening of the binding pocket narrows from ~15 Å to ~12 Å in the probenecid-bound state.

• Dual-Pathway Blockade: The cytosolic entrance is split into two paths. Probenecid binding critically affects both:

• Path A (between TM2 and TM11) is narrowed from ~5 Å to ~4 Å.

• Path B (between TM5 and TM8) is completely blocked. Restriction of the access route to path B likely limits the entry of substrates to Site 1 and the exit of substrates from the binding pocket.

This structural rearrangement is caused by a slight inward movement of the cytoplasmic ends of TM5, TM8, TM10, and TM11 toward the binding pocket.

3. Locked Conformation

By constricting the cytoplasmic access routes, probenecid does not just compete for the substrate-binding site; it stabilizes the transporter in an apo-like, inward-facing conformation that is inaccessible to cytosolic substrates. This prevents the entry of new substrates and likely traps the transporter in this non-functional state, effectively "locking" it and preventing the conformational changes necessary for the transport cycle.

Mechanistic Insights into hOAT1 Function and Inhibition

Fig 2. Mechanism of olmesartan binding and conformational inhibition by probenecid. A) When the transporter is in its outward-facing conformation, substrates or inhibitors enter the central binding pocket and undergo structural rearrangement to the inward-facing conformation. When olmesartan interacts with the bottom gating residues M207 and F442, the side chains S203, Y230 (not shown here), and R466 appear to rearrange to coordinate with a chloride ion and drug compared to the apo structure. Whereas probenecid binding induces an additional conformation change for inhibition (apo-like conformation).

1. A Dual-Mechanism for Potent Inhibition by Probenecid

The study reveals that the classic inhibitor probenecid employs a sophisticated, dual-mechanism to arrest OAT1 function, moving beyond simple competition.

Direct Competition: Probenecid occupies the central binding pocket, and its interaction with K382 in Site 1 directly competes with the binding of the counter-substrate α-ketoglutarate (α-KG). This disrupts the exchange cycle that drives substrate transport.

Conformational Arrest: More significantly, probenecid binding induces subtle conformational changes in the cytoplasmic ends of transmembrane helices (TM5, TM8, TM10, TM11). This leads to a constriction of the cytosolic opening, completely blocking one access path (Path B) and narrowing the other (Path A). This physically prevents substrates from entering or exiting the binding site from the cytoplasm, effectively "locking" the transporter in an inactive, inward-facing state. This mechanism is reminiscent of inhibition seen in other transporters like hURAT1, suggesting it may be a general strategy for effective transport arrest.

2. Structural Basis for Species-Specific Drug Transport

A major advancement of this work is the structural explanation for long-observed differences in drug handling between human OAT1 and animal orthologs.

The Critical Role of S203: The residue S203 in hOAT1 (which is an alanine, A203, in rat OAT1) is identified as a key species-specific determinant. It does not contact substrates like olmesartan directly. Instead, its hydroxyl group is crucial for coordinating a chloride ion along with residues Y230 and R466.

Chloride Coordination Enhances Substrate Affinity: This chloride coordination network stabilizes the binding of certain substrates. Functional data confirms that the S203A mutation drastically reduces olmesartan affinity specifically in the presence of chloride. This explains why drugs like olmesartan and tenofovir show different transport kinetics between species; the human transporter, with its S203, has a enhanced, chloride-dependent mechanism for high-affinity binding that the rat ortholog lacks.

Notes & References

1. ↑ Cryo-EM structures of human OAT1 reveal drug binding and inhibition mechanisms https://doi.org/10.1016/j.str.2025.07.019
2. ↑ Molecular cloning and characterization of a novel liver-specific transport protein https://doi.org/10.1242/jcs.107.4.1065
3. ↑ Molecular Cloning and Characterization of NKT, a Gene Product Related to the Organic Cation Transporter Family That Is Almost Exclusively Expressed in the Kidney https://doi.org/10.1074/jbc.272.10.6471
4. ↑ Ingraham, L., Li, M., Renfro, J.L., Parker, S., Vapurcuyan, A., Hanna, I., and Pelis, R.M. (2014). A plasma concentration of α-ketoglutarate influences the kinetic interaction of ligands with organic anion transporter 1. Mol. Pharmacol. 86, 86–95. https://doi.org/10.1124/mol.114.091777.
5. ↑ Uwai, Y., Kawasaki, T., and Nabekura, T. (2017). D-Malate decreases renal content of α-ketoglutarate, a driving force of organic anion transporters OAT1 and OAT3, resulting in inhibited tubular secretion of phenolsulfonphthalein, in rats. Biopharm. Drug Dispos. 38, 479–485. https://doi.org/10. 1002/bdd.2089.