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Prakash, M. K.

Publications and source records attributed to Prakash, M. K..

6 recordsLinked to original sources

One drug multiple targets: An approach to predict drug efficacies on bacterial strains differing in membrane composition

Rational design methodologies such as quantitative structure activity relationships (QSAR) have conventionally focused on screening through several drugs for their activity against a single target, either a bacterial protein or membrane. Recent concerns in drug design such as the development of drug resistance by membrane adaptation, or the undesirable damage to gut microbiota require a paradigm shift in activity prediction. A complementary approach capable of predicting the activity of a single drug against diverse targets, the diversity arising from bacterial adaptation or a heterogeneous composition with other helpful or harmful bacteria, is needed. As a first predictive step towards this goal, we develop a quantitative model for the activity of daptomycin on Streptococcus aureus strains with different membrane compositions, mainly varying in lysylation. The results of the predictions are good, and within the limits of the scarcely available data, hint at an interaction of daptomycin with the inner membrane. The complementary approach may in principle be extended to estimate the activity against gut bacterial membranes, when systematic data can be curated for training the model.

biochemistry

Computationally designing antimicrobial peptides for Acinectobacter Baumannii

Acinetobacter Baumannii, which is mostly contracted in hospital stays, has been developing resistance to all available antibiotics, including the last line of drugs, such as carbapenem. Because of its quick adaptation there is an immediate need to design new antibiotics, possibly antimicrobial peptides (AMPs) to which bacteria do not develop resistance easily. Our threefold goal was to curate the available activity of AMPs on the same strain of A. Baumannii, build a neural network model for predicting their activity and use it to rationally pre-screen for lead generation from the thousands of naturally occurring AMPs. By curating and analyzing the recent activity data from 81 AMPs on ATCC 19606 strain, we develop a quantitative AMP activity prediction model. We selected three other models with comparable performance against a test set with known activities. With the goal of inspiring further studies on AMP drug candidates and their rational shortlisting, we made activity predictions for the entire database of AMPs using all the models. To handle the uncertainty of training with a small data set, highlighted peptides which had consistent results from all models.

biochemistry

Visualizing Deep Mutational Scan Data

Site-directed and random mutagenesis are biochemical tools to obtain insights into the structure and function of proteins. Recent advances such as deep mutational scan have allowed a complete scan of all the amino acid positions in a protein with each of the 19 possible alternatives. Mapping out the phenotypic consequences of thousands of single point mutations in the same protein is now possible. Visualizing and analysing the rich data offers an opportunity to learn more about the effects of mutations, for a better understanding and engineering of proteins. This work focuses on such visualization analyses applied to the mutational data of TEM-1 {beta}-lactamase. The data is examined in the light of the expected biochemical effects of single point mutations, with the goal of reinforcing or retraining the intuitions. Individual attributes of the amino acid mutations such as the solvent accessible area, charge type change, and distance from the catalytic center capture most of the relevant functional effects. Visualizing the data suggests how combinations of these attributes can be used for a better classification of the effects of mutations, when independently they do not offer a high predictability.

biochemistry

Exploring the context of diacidic motif D-E as a signal for unconventional protein secretion in eukaryotic proteins

Unconventional protein secretion (UPS) is an important phenomenon with fundamental implications to cargo export. How eukaryotic proteins transported by UPS are recognized without a conventional signal peptide has been an open question. It was recently observed that a diacidic amino acid motif (ASP-GLU or DE) is necessary for the secretion of superoxide dismutase 1 (SOD1) from yeast under nutrient starvation. Taking cue from this discovery, we explore the hypothesis of whether the diacidic motif DE, which can occur fairly ubiquitously, along with its context, can be a generic signal for unconventional secretion of proteins. Two different definitions of context were evaluated: structural order and charge signature in the neighborhood of DE as one, and the nature of the amino acid insertion ( X) when a D-X-E motif is present, as another. We observe that among the eukaryotic proteins we studied, the odds of the protein being secreted are higher when the DE motif occurs in the disordered region of the protein, with higher hydrophobicity and lower charge or when the insertion X has a propensity for phosphorylation.

cell biology

Viral Complexity: Amino acid co-evolution in viral genomes as a possible metric

Viruses are simultaneously simple and complex. Simple because they have barely around ten types of proteins compared to tens of thousands of proteins in bacteria. Complex because amino acid mutation rates are very high, challenging host immune system and drugs. In this work we use the co-evolution of amino acids and the network characteristics that arise out of it to describe the complexity hidden in the multitude of variations in a viral genome. Using large-scale genomic data, the complexity in several viruses was compared. Interestingly, the co-evolutionary relations were primarily intra-protein in avian influenza and inter-protein in HIV-1. The network degree distributions showed two universality classes: a power-law with exponent -1 in HIV-1 and avian-influenza, random co-evolutionary behavior in human flu and dengue, suggesting the co-evolution as one way to statistically classify the complexity in viruses. The observed correlation between the network densities and the strengths on virus Richter scale raises interesting questions on whether it is possible to define the complexity of viruses using their evolutionary networks.

systems biology

Deep2Full: Predictive model for complementing phenotypic outcomes in a deep mutational scan using protein sequence and structure information

Large scale mutagenesis experiments are becoming possible owing to the advancement in the sequencing technologies and high throughput screening. Deep mutational scans perform exhaustive single-point muta-tions on a protein and probe their phenotypic effects. Performing a full scan with site-directed mutations of all the amino acid residues in a protein may not be practical, and may not even be required, especially if predictive computational models can be developed. Computational models are however naive to cellular response in the myriads of assay-conditions. In order to develop the realistic paradigm of assay context-aware predictive hybrid models, we combine minimal deep mutational studies with computational models and pre-dict the phenotypic outcomes quantitatively. Structural, sequence and co-evolutionary information along with partial deep mutational scan data was included to capture the phenotypic relevance of the mutations to the specific screening criterion. The model reliably predicts the fitness outcomes of hundreds of randomly selected amino acid mutations in {beta}-lactamase, when the phenotypic fitness data from as few as 15% of the full mutation is available. Interestingly, the predictive capabilities are better with a random set of mutations rather than with a systematic substitution of all amino acids to alanine, asparagine and histidine (ANH). The model can potentially be extended for predicting the phenotypic outcomes at other concentrations of the stressor by carefully analyzing the dose-response curves of a representative set of mutations.\n\nAuthor SummaryMutations are the minor changes in protein sequences, with incommensurately high consequences for their function. Many severe diseases can occur with simple single point mutations. An interesting way of studying these mutations is not to isolate the protein from its natural conditions, but rather study how the fitness of the cell improves or decreases in response to these mutations. Whether it is for understanding disease biology or for bio-engineering applications it is important to quantify the impact of mutations on the cellular fitness. An experimental paradigm has evolved which has improved the ability to sample several hundred thousands of mutation-fitness relations using high throughput screening. However, since these are very specialized experiments, the question is if the number of such experiments required can be minimized, by using computer models to complement the rest of the fitness predictions. In this work we introduce this new paradigm which uses computer model trained on a partial deep mutation scan data, to predict the fitness variations in a full mutations scan that could also be repeated under multiple experimental conditions like drug concentrations.

bioinformatics