Protein quantification is traditionally performed through enzyme-linked immunosorbent assay (ELISA), which involves long preparation times. To overcome this, new approaches use aptamers as an alternative to antibodies. In this paper, we present a new approach to quantify proteins with short DNA aptamers through polymerase chain reaction (PCR) resulting in shorter protocol times with comparatively improved limit of detection. The proposed method includes a novel way to quantify both the target protein and corresponding short DNA-aptamers simultaneously, which also allows to fully characterise the performance of aptasensors. Human leptin is used as a target protein to validate this technique, because it is considered an important biomarker for obesity-related studies. In our experiments we achieved a lowest limit of detection of 100 pg/mL within less than two hours, a limit affected by the dissociation constant 1 of the leptin aptamer, which could be improved by selecting a more specific aptamer.Because of the simple and inexpensive approach, this technique can be employed for Lab-On-Chip implementations and for rapid 'on-site' quantification of proteins.
The negative effect of sedentary behaviour on type 2 diabetes markers is established, but the interaction with measures of physical activity is still largely unknown. Previous studies have analysed associations with single-activity models, which ignore the interaction with other behaviours. By including results from various analytical approaches, this review critically summarises the effects of sedentary behaviour on diabetes markers and the benefits of substitutions and compositions of physical activity. Ovid Medline, Embase and Cochrane Library databases were systematically searched. Studies were selected if sedentary behaviour and physical activity were measured by accelerometer in the general population, and if associations were reported with glucose, insulin, HOMA-IR, insulin sensitivity, HbA1c, diabetes incidence, CRP and IL-6. Forty-five studies were included in the review. Conclusive detrimental associations with sedentary behaviour were determined for 2-h insulin (6/12 studies found associations), fasting insulin (15/19 studies), insulin sensitivity (4/6 studies), diabetes (3/4 studies) and IL-6 (2/3 studies). Reallocating sedentary behaviour to light or moderate-to-vigorous activity has a beneficial effect for 2-h glucose (1/1 studies), fasting insulin (3/3 studies), HOMA-IR (1/1 studies) and insulin sensitivity (1/1 studies). Compositional measures of sedentary behaviour were found to affect 2-h glucose (1/1 studies), fasting insulin (2/3 studies), 2-h insulin (1/1 studies), HOMA-IR (2/2 studies) and CRP (1/1 studies). Different analytical methods produced conflicting results for fasting glucose, 2-h glucose, 2-h insulin, insulin sensitivity, HOMA-IR, diabetes, hbA1c, CRP and IL-6. Studies analysing data by quartiles report independent associations between sedentary behaviour and fasting insulin, HOMA-IR and diabetes only for high duration of sedentary time (7–9 hours/day). However, this review could not provide sufficient evidence for a time-specific cut-off of sedentary behaviour for diabetes biomarkers. While substituting sedentary behaviour with moderate-to-vigorous activity brings greater improvements for health, light activity also benefits metabolic health. Future research should elucidate the effects of substituting and combining different activity durations and modalities.
The first evidence for X(3872) production in relativistic heavy ion collisions is reported. The X(3872) production is studied in lead-lead (Pb-Pb) collisions at a center-of-mass energy of ffiffiffiffiffiffiffi ffi s NN p ¼ 5.02 TeV per nucleon pair, using the decay chain Xð3872ÞThe data were recorded with the CMS detector in 2018 and correspond to an integrated luminosity of 1.7 nb −1 . The measurement is performed in the rapidity and transverse momentum ranges jyj < 1.6 and 15 < p T < 50 GeV=c. The significance of the inclusive X(3872) signal is 4.2 standard deviations. The prompt X(3872) to ψ2S yield ratio is found to be ρ Pb-Pb ¼ 1.08 AE 0.49ðstatÞ AE 0.52ðsystÞ, to be compared with typical values of 0.1 for pp collisions. This result provides a unique experimental input to theoretical models of the X(3872) production mechanism, and of the nature of this exotic state.
In this paper we present the design of a new pointof-care device for protein quantification. The proposed design is based on a novel aptamer-mediated methodology and real time polymerase chain reaction (RT-PCR), a robust and ultrasensitive method for DNA amplification, which we employ for very sensitive quantification of proteins. In addition, we have also developed an algorithm for the processing of raw fluorescence data from the portable RT-PCR device. The algorithm leads to better linearity than a proprietary software from a commercially available RT-PCR machine. The modular nature of the system allows for easy assembly and adjustment towards a variety of biomarkers for applications in disease diagnosis and personalised medicine.
The modern sedentary lifestyle is negatively influencing human health, and the current guidelines recommend at least 150 min of moderate activity per week. However, the challenge is how to measure human activity in a practical way. While accelerometers are the most common tools to measure activity, current activity classification methods require calibration studies or labelled datasets—requirements that slow the research progress. Therefore, there is a pressing need to classify and quantify human activity efficiently. In this work, we propose an unsupervised approach to classify activities from accelerometer data using hidden semi-Markov models. We tune and infer the model parameters on accelerometer data from the UK Biobank and select the optimal model based on features used and informativeness of the prior. The best model achieves an average correlation of 0.4 between the inferred activities and the reference ones, with the overall physical activity obtaining a correlation of 0.8. Additionally, to prove the clinical significance of the method, we validate it by performing a linear regression between the inferred activities and anthropometric measures such as BMI and waist circumference. We show that for a sedentary behaviour and total physical activity, the proposed method achieves comparable regression coefficients to the reference labelled dataset. Moreover, the proposed method achieves a good agreement with a labelled dataset for daily time spent in a sedentary behaviour and total physical activity. The unsupervised nature of the method allows for a data-driven classification that does not require calibration studies or labelled datasets and can thus facilitate both clinical research as well as lifestyle recommendations.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.