Motivation: Cardiovascular disease is the primary cause of death globally accounting for approximately 17.7 million deaths per year. One of the stakes linked with cardiovascular diseases and other complications is hypertension. Naturally derived bioactive peptides with antihypertensive activities serve as promising alternatives to pharmaceutical drugs. So far, there is no comprehensive analysis, assessment of diverse features and implementation of various machine-learning (ML) algorithms applied for antihypertensive peptide (AHTP) model construction. Results: In this study, we utilized six different ML algorithms, namely, Adaboost, extremely randomized tree (ERT), gradient boosting (GB), k-nearest neighbor, random forest (RF) and support vector machine (SVM) using 51 feature descriptors derived from eight different feature encodings for the prediction of AHTPs. While ERT-based trained models performed consistently better than other algorithms regardless of various feature descriptors, we treated them as baseline predictors, whose predicted probability of AHTPs was further used as input features separately for four different ML-algorithms (ERT, GB, RF and SVM) and developed their corresponding meta-predictors using a two-step feature selection protocol. Subsequently, the integration of four meta-predictors through an ensemble learning approach improved the balanced prediction performance and model robustness on the independent dataset. Upon comparison with existing methods, mAHTPred showed superior performance with an overall improvement of approximately 6–7% in both benchmarking and independent datasets. Availability and implementation: The user-friendly online prediction tool, mAHTPred is freely accessible at http://thegleelab.org/mAHTPred. Supplementary information: Supplementary data are available at Bioinformatics online.

Air pollution exerts several deleterious effects on the cardiovascular system, with cardiovascular disease (CVD) accounting for 80% of all premature deaths caused by air pollution. Short-term exposure to particulate matter 2.5 (PM_2.5) leads to acute CVD-associated deaths and nonfatal events, whereas long-term exposure increases CVD-associated risk of death and reduces longevity. Here, we summarize published data illustrating how PM_2.5 may impact the cardiovascular system to provide information on the mechanisms by which it may contribute to CVDs. We provide an overview of PM_2.5, its associated health risks, global statistics, mechanistic underpinnings related to mitochondria, and hazardous biological effects. We elaborate on the association between PM_2.5 exposure and CVD development and examine preventive PM_2.5 exposure measures and future strategies for combating PM_2.5-related adverse health effects. The insights gained can provide critical guidelines for preventing pollution-related CVDs through governmental, societal, and personal measures, thereby benefitting humanity and slowing climate change.

The use of therapeutic peptides in various inflammatory diseases and autoimmune disorders has received considerable attention; however, the identification of anti-inflammatory peptides (AIPs) through wet-lab experimentation is expensive and often time consuming. Therefore, the development of novel computational methods is needed to identify potential AIP candidates prior to in vitro experimentation. In this study, we proposed a random forest (RF)-based method for predicting AIPs, called AIPpred (AIP predictor in primary amino acid sequences), which was trained with 354 optimal features. First, we systematically studied the contribution of individual composition [amino acid-, dipeptide composition (DPC), amino acid index, chain-transition-distribution, and physicochemical properties] in AIP prediction. Since the performance of the DPC-based model is significantly better than that of other composition-based models, we applied a feature selection protocol on this model and identified the optimal features. AIPpred achieved an area under the curve (AUC) value of 0.801 in a 5-fold cross-validation test, which was ∼2% higher than that of the control RF predictor trained with all DPC composition features, indicating the efficiency of the feature selection protocol. Furthermore, we evaluated the performance of AIPpred on an independent dataset, with results showing that our method outperformed an existing method, as well as 3 different machine learning methods developed in this study, with an AUC value of 0.814. These results indicated that AIPpred will be a useful tool for predicting AIPs and might efficiently assist the development of AIP therapeutics and biomedical research. AIPpred is freely accessible at www.thegleelab.org/AIPpred.

DNA N4-methylcytosine (4mC) is an important genetic modification and plays crucial roles in differentiation between self and non-self DNA and in controlling DNA replication, cell cycle, and gene-expression levels. Accurate 4mC site identification is fundamental to improve the understanding of 4mC biological functions and mechanisms. Hence, it is necessary to develop in silico approaches for efficient and high-throughput 4mC site identification. Although some bioinformatic tools have been developed in this regard, their prediction accuracy and generalizability require improvement to optimize their usability in practical applications. For this purpose, we here proposed Meta-4mCpred, a meta-predictor for 4mC site prediction. In Meta-4mCpred, we employed a feature representation learning scheme and generated 56 probabilistic features based on four different machine-learning algorithms and seven feature encodings covering diverse sequence information, including compositional, physicochemical, and position-specific information. Subsequently, the probabilistic features were used as an input to support vector machine and developed a final meta-predictor. To the best of our knowledge, this is the first meta-predictor for 4mC site prediction. Cross-validation results show that Meta-4mCpred achieved an overall average accuracy of 84.2% from six different species, which is ∼2%-4% higher than those attainable using the state-of-the-art predictors. Furthermore, Meta-4mCpred achieved an overall average accuracy of 86% on independent datasets evaluation, which is over 4% higher than those yielded by the state-of-the-art predictors. The user-friendly webserver employed to implement the proposed Meta-4mCpred is freely accessible at http://thegleelab.org/Meta-4mCpred.