Move-Biased Monte Carlo Simulation Method for Protein Native Structure Prediction

ABSTRACT

Proteins are polymers of Amino Acid (AA) which are constructed after translation of genetic code in DNA of organisms, and have functionality that depends on their Native Structure (NS). Experimental methods for protein NS determination are complicated, expensive and timeconsuming. Consequently, Computational Methods (CM), including Monte Carlo (MC), aim to circumvent these challenges. However, the MC is complex and inconsistent in NS Prediction (NSP). This study was designed to develop a Move-Biased MC (MBMC) simulation algorithm that may simplify the complexity of existing MC and makes it consistent for NSP. Protein was described as a coarse-grained structure and folding as Self-Avoiding Walks (SAW) on square lattices. Relative Probability Parameters (RPP) were introduced to determine natural probabilities of protein conformations from SAW and to simulate the desired sequence length from RPP optimal combination. Thereafter, a graphical algorithm was developed to group the SAW steps into hydrophobic and polar AA units according to the Hydrophobic-Polar (HP) model. The MBMC method was developed as a coupling of diagonal-pull Move-Biased (MB) on the lowest energy SAW conformation. The materials for testing the MBMC method included eight Benchmark Sequences (BMS) from the protein data bank such as SI-1, SI-2, SI-3, SI-4, SI5, SI-6, SI-7, and SI-8 with sequence lengths 20, 24, 25, 36, 48, 60, 64, and 85 nm, respectively. The lowest energy (consistency in prediction of NS), computation time and algorithmic steps of the MBMC method was compared with some existing methods [such as Conventional MC (CMC), Genetic Algorithm (GA), Evolutionary MC (EMC), Ant Colony Optimization (ACO), Hybrid Elastic Net Algorithm (ENA)]. Data were analysed using inferential statistics. The optimal combination of the RPP for the MBMC algorithm were 0.71, 0.02, 0.25 and 0.02 for up, down, left and right orientations, respectively. The energies of the NS obtained from the MBMC method were -9, -9, -8, -14, -23, -35, -42 and -52 J for the BMS, respectively. In contrast, for GA energies derived were -9, -9, -8, -12, -22, -34, -37, and no record for eighth BMS; for ACO they were -9, -9, -8, -14, -23, -34, -32, -53; for EMC they were -9, -9, -8, -14, - 23, -35, -39 and -52; for ENA they were -9, -9, -8, -14, -23, -36, -39, and no record for eighth BMS; for CMC they were -9, -9, -7, -12, -20, -33, -35, and no record for the eighth BMS. Also, MBMC method consistently predicted the NS of the BMS in 8.90, 8.51, 8.37, 9.14, 9.45, 9.46, 9.52, and 12.85 seconds, respectively. In contrast the computation times for GA were only reported for the first four BMS as 5.60, 6.00, 3.66, 54.60 seconds, and no record of computational time for the CMC and EMC Benchmark sequences, respectively. Moreover, MBMC has fewer algorithmic steps and simpler simulation procedure than CMC, GA, EMC and ENA methods. The developed Move-Biased Monte Carlo method had simpler algorithmic steps than the existing Monte Carlo methods and consistently predicted the native structure of proteins faster than existing algorithms.