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Murad Nayal, Barry Honig Columbia University, NY

On the nature of cavities on protein surfaces: Application to the Identification of drug-binding sites. Murad Nayal, Barry Honig Columbia University, NY Proteins: Structure, Function and Bioinformatics, Accepted 15 Nov. 05. Ankur Dhanik. Abstract.

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Murad Nayal, Barry Honig Columbia University, NY

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  1. On the nature of cavities on protein surfaces: Application to the Identification of drug-binding sites Murad Nayal, Barry Honig Columbia University, NY Proteins: Structure, Function and Bioinformatics, Accepted 15 Nov. 05 Ankur Dhanik

  2. Abstract • Identification of drug-binding sites useful for virtual screening and drug design. • Small ligands are known to bind proteins at surface cavities. • Two tasks: identification of cavities and prediction of their drugabbilities (whether the cavity is suitable for drug binding). • The method presented in this paper encoded in program called SCREEN (Surface Cavity REcognition and EvaluatioN).

  3. Abstract • SCREEN works by first constructing two molecular surfaces using GRASP: a conventional molecular surface (MS) using a 1.4 A radius and a second low resolution envelope using a large probe sphere, which serves as ‘sea-level’. Depth of each vertex of MS is computed and compared with threshold. • For each surface cavity, 408 attributes are computed (physiochemical, structural, and geometric). • Random Forests based classifier is used. • Training data set is derived from a collection of 100 nonredundant protein ligand complexes.

  4. Results • SCREEN predicts drug binding cavities with a balanced error rate of 7.2% and coverage of 88.9%, while a CASTp ( a popular protein cavity detection program) based druggability predictor (using cavity size criteria alone) predicts with a balanced error rate of 15.7% and coverage of 71.7%. • SCREEN predicts drug-binding cavities missed by cavity size criteria (three examples). • Out 18 attributes out of 408 used, were found to be significant predictors of drug binding cavities. • It follows from the above that drug binding cavities are large, deep, have an intricate curvature profile, are rigid, and have a relatively small number of prolines, as well as amino acids with small but negative octanol-to-water transfer free energies (Asn, Gln, Glu).

  5. Results Protein-tyrosine phosphatase 1B, PTP1B (PDB code: 1l8g). The largest surface cavity (colored green: area, 184 Å2; volume, 400 Å3; residues Gln78, Arg79, Ser80, and Pro210) is about 20 Å from the ligand-binding site. The drug binds at the second largest cavity, colored red, as predicted (area, 170 Å2; volume, 259 Å3; residues Gln262, Ala217, Ile219, Val49, and Asp181).

  6. Results Human carbonic anhydrase II (CA II). The largest cavity (area, 281 Å2; volume, 679 Å3; residues Phe213, Tyr7, Gly8, Asp243, and Lys170), shown in green, is rather shallow and is predicted not to bind a drug. Instead, the second largest cavity (area, 194 Å2; volume, 281 Å3; residues Leu198, Thr200, His94, Val121, and His64) is the one predicted correctly to bind the drug.

  7. Results Human factor Xa complexed with inhibitor RPR128515 (PDB code: 1ezq). Four cavities ranked 1, 2, 3, and 9, shown here in red, were predicted to be potential drug-binding cavities. The ligand actually binds at two cavities, 3 (the S1 pocket: area, 274 Å2; volume, 384 Å3; residues Gln192, Trp215, Ser195, Cys191, Gly216, and Asp) and 9 (the S4 pocket: area, 69 Å2; volume, 155 Å3; residues Trp215, Phe174, Thr98, Tyr99, and Ile175).

  8. Results

  9. Comments • The prediction of drug-binding cavities was done without considering the nature of the drug. • Physicochemical cavity properties were not found useful. • Perhaps they can play an important role when surface cavities that recognize a particular ligand are characterized. • Energy-based approach offers a promising alternative to geometry-based methods

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