Highly Stretchable Waterproof Fiber Asymmetric Supercapacitors in an Integrated Structure

Fiber supercapacitors have attracted tremendous attention as promising power source candidates for the next generation of wearable electronics, which are flexible, stretchable, and washable. Although asymmetric fiber supercapacitors with a high energy density have been achieved, their stretchability is no more than 200%, and they still face mechanical instability and an unreliable waterproof structure. This work develops a highly integrated structure for a waterproof, highly stretchable, and asymmetric fiber-shaped supercapacitor, which is assembled by integrating a helix-shaped asymmetric fiber supercapacitor into a bifunctional polymer. The asymmetric fiber supercapacitor demonstrates a working voltage of 1.6 V, a high energy density of 2.86 mW h/cm³, has unchanged capacitance after being immersed in water for 50 h, and retains 95% of its initial capacitance after 3000 cycles of stretching–releasing at a maximum strain of 400%. The extraordinary waterproof capability, the large stretching strain, and excellent stretching stability are attributed to the highly integrated structure design, which can also simplify the assembly process of stretchable, waterproof fiber supercapacitors

Nanocellulose-Assisted Growth of Manganese Dioxide on Thin Graphite Papers for High-Performance Supercapacitor Electrodes

High volumetric energy density, based on the entire electrodes, is necessary for the miniaturization of supercapacitors. The growth of manganese dioxide (MnO₂) on graphite papers via chemical reactions was very limited, resulting in the inferior volumetric-specific capacitance. Cellulose nanofibers, coated on graphite papers, impressively enhanced the thickness of grown MnO₂ layers and, thus, volumetric-specific capacitance. The symmetric supercapacitors displayed an extremely high volumetric energy density of 10.6 mWh/cm³ at a power density of 0.11 W/cm³. The performance was superior to that of MnO₂-based symmetric and even asymmetric devices in the past studies. This research opens a new opportunity to fabricate high-performance supercapacitor electrodes by utilizing cellulose nanofibers detached from natural cellulose

HLA Class I and II Blocks Are Associated to Susceptibility, Clinical Subtypes and Autoantibodies in Mexican Systemic Sclerosis (SSc) Patients

<div><p>Introduction</p><p>Human leukocyte antigen (HLA) polymorphism studies in Systemic Sclerosis (SSc) have yielded variable results. These studies need to consider the genetic admixture of the studied population. Here we used our previously reported definition of genetic admixture of Mexicans using HLA class I and II DNA blocks to map genetic susceptibility to develop SSc and its complications.</p><p>Methods</p><p>We included 159 patients from a cohort of Mexican Mestizo SSc patients. We performed clinical evaluation, obtained SSc-associated antibodies, and determined HLA class I and class II alleles using sequence-based, high-resolution techniques to evaluate the contribution of these genes to SSc susceptibility, their correlation with the clinical and autoantibody profile and the prevalence of Amerindian, Caucasian and African alleles, blocks and haplotypes in this population.</p><p>Results</p><p>Our study revealed that class I block HLA-C*12:03-B*18:01 was important to map susceptibility to diffuse cutaneous (dc) SSc, HLA-C*07:01-B*08:01 block to map the susceptibility role of HLA-B*08:01 to develop SSc, and the C*07:02-B*39:05 and C*07:02-B*39:06 blocks to map the protective role of C*07:02 in SSc. We also confirmed previous associations of HLA-DRB1*11:04 and –DRB1*01 to susceptibility to develop SSc. Importantly, we mapped the protective role of DQB1*03:01 using three Amerindian blocks. We also found a significant association for the presence of anti-Topoisomerase I antibody with HLA-DQB1*04:02, present in an Amerindian block (DRB1*08:02-DQB1*04:02), and we found several alleles associated to internal organ damage. The admixture estimations revealed a lower proportion of the Amerindian genetic component among SSc patients.</p><p>Conclusion</p><p>This is the first report of the diversity of HLA class I and II alleles and haplotypes Mexican patients with SSc. Our findings suggest that HLA class I and class II genes contribute to the protection and susceptibility to develop SSc and its different clinical presentations as well as different autoantibody profiles in Mexicans.</p></div

Frequency of SSc-associated autoantibodies in our SSc patients.

<p>dcSSc: diffuse cutaneous systemic sclerosis, lcSSc: limited cutaneous systemic sclerosis, Anti-RNA Pol III: anti-RNA polymerase I/III.</p><p>Frequency of SSc-associated autoantibodies in our SSc patients.</p

HLA class II genes associations with specific autoantibodies in SSc.

<p>anti-RNAP I/III: anti-RNA polymerase I/III.</p><p>HLA class II genes associations with specific autoantibodies in SSc.</p

Allele-Level Haplotype Frequencies and Pairwise Linkage Disequilibrium for 14 KIR Loci in 506 European-American Individuals

<div><p>The immune responses of natural killer cells are regulated, in part, by killer cell immunoglobulin-like receptors (KIR). The 16 closely-related genes in the KIR gene system have been diversified by gene duplication and unequal crossing over, thereby generating haplotypes with variation in gene copy number. Allelic variation also contributes to diversity within the complex. In this study, we estimated allele-level haplotype frequencies and pairwise linkage disequilibrium statistics for 14 KIR loci. The typing utilized multiple methodologies by four laboratories to provide at least 2x coverage for each allele. The computational methods generated maximum-likelihood estimates of allele-level haplotypes. Our results indicate the most extensive allele diversity was observed for the KIR framework genes and for the genes localized to the telomeric region of the KIR A haplotype. Particular alleles of the stimulatory loci appear to be nearly fixed on specific, common haplotypes while many of the less frequent alleles of the inhibitory loci appeared on multiple haplotypes, some with common haplotype structures. Haplotype structures cA01 and/or tA01 predominate in this cohort, as has been observed in most populations worldwide. Linkage disequilibrium is high within the centromeric and telomeric haplotype regions but not between them and is particularly strong between centromeric gene pairs <em>KIR2DL5</em>∼<em>KIR2DS3S5</em> and <em>KIR2DS3S5</em>∼<em>KIR2DL1,</em> and telomeric <em>KIR3DL1</em>∼<em>KIR2DS4</em>. Although 93% of the individuals have unique pairs of full-length allelic haplotypes, large genomic blocks sharing specific sets of alleles are seen in the most frequent haplotypes. These high-resolution, high-quality haplotypes extend our basic knowledge of the KIR gene system and may be used to support clinical studies beyond single gene analysis.</p> </div

Demographic data and organ damage according to the modified Medsger’s Severity Scale.

<p>dcSSc: diffuse cutaneous systemic sclerosis, lcSSc: limited cutaneous systemic sclerosis, ILD: interstitial lung disease; PAH: pulmonary arterial hypertension.</p><p>Demographic data and organ damage according to the modified Medsger’s Severity Scale.</p

Principal component analysis (PCA) plot reveals a close genetic relationship of Mexican admixed SSc patients and healthy controls (HC) from Mexico City to Native American groups.

<p>Native American populations are represented in the upper left of the graphic and Caucasian components in the right bottom area of the graphic. Amerindian components are represented in the left bottom area. Red and blue dots represent difusse and limited SSc patients respectively and the total group in represented in green. The different populations included in the PCA analysis were: Ire: Ireland, Eng: England, Ger: Germany, Aus: Austria; Spa: Spain, Ita: Italy, UK: United Kingdom, Fra: France, Azo: Azores, Sao: São Tomé Island, Cam: Cameroon, Mal: Mali, Zam: Zambia, KLu: Luo from Kenia, KNa: Nandi from Kenia, Sen: Senegal, Gui: Guinea Bissau, Tar: Tarahumara, Gil: Native Americans from Gila River, Yup: Yu’pik from Alaska, Mit: Mixtec from Oaxaca, Zap: Zapotec from Oaxaca, Mix: Mixe from Oaxaca, Ser: Seri from Sonora, Nav: Navajo from New Mexico, HC: “Mexican Admixed controls” [<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0126727#pone.0126727.ref026" target="_blank">26</a>].</p

Overall linkage disequilibrium.

<p>Wn is displayed for each gene pair in a full-length KIR haplotype. Lighter shades indicate lower linkage disequilibrium and represent Wn approaching 0. Darker shades indicate higher linkage disequilibrium and represent Wn values approaching 1. Since they are now considered to be a single locus, <i>KIR2DL2</i> and <i>KIR2DL3</i> were combined into <i>KIR2DL2L3</i>; similarly, <i>KIR2DS3</i> and <i>KIR2DS5</i> were combined into <i>KIR2DS3S5.</i></p

Gene-content haplotype frequencies.

<p>Estimated frequencies for each centromere, telomere, and full reference haplotype. LD (D’) is included for each pairing of centromere and telomere. Haplotypes with frequencies less than 1% where determined by physical linkage and gene copy number of <i>KIR2DS4</i>.</p