17 research outputs found
Steady state current transfer and scattering theory
The correspondence between the steady state theory of current transfer and
scattering theory in a system of coupled tight-binding models of 1-dimensional
wires is explored. For weak interwire coupling both calculations give nearly
identical results, except at singular points associated with band edges. The
effect of decoherence in each of these models is studied using a generalization
of the Liouville-von Neuman equation suitable for steady-state situations. An
example of a single impurity model is studied in details, leading to a lattice
model of scattering off target that affects both potential scattering and
decoherence. For an impurity level lying inside the energy band, the
transmission coefficient diminishes with increasing dephasing rate, while the
opposite holds for impurity energy outside the band. The efficiency of current
transfer in the coupled wire system decreases with increasing dephasing.Comment: 22 pages, 13 figure
Steady state theory of current transfer
Current transfer is defined as a charge transfer process where the
transferred charge carries information about its original motion. We have
recently suggested that such transfer causes the asymmetry observed in electron
transfer induced by circularly polarized light through helical wires. This
paper presents the steady state theory of current transfer within a tight
binding model of coupled wires systems. The efficiency of current transfer is
quantified in terms of the calculated asymmetry in the system response to a
steady current imposed on one of the wires, with respect to the imposed current
direction.Comment: 25 pages, 14 figure
Presentation Mode of Glycans Affect Recognition of Human Serum anti-Neu5Gc IgG Antibodies
Recognition of carbohydrates by antibodies can be affected by antigen composition and density. This had been investigated in a variety of controllable multivalent systems using synthetic carbohydrate antigens, yet such effects on anticarbohydrate antibodies in circulating human serum have not been fully addressed thus far. All humans develop a polyclonal and diverse response against carbohydrates containing a nonhuman sialic acid form, N-glycolylneuraminic acid (Neu5Gc). This red meat-derived monosaccharide is incorporated into a diverse collection of human glycans resulting in circulating anti-Neu5Gc antibodies in human sera. Such antibodies can cause exacerbation of diseases mediated by chronic inflammation such as cancer and atherosclerosis. We aimed to evaluate how different presentation modes of Neu5Gc-glycans can affect the detection of anti-Neu5Gc IgGs in human serum. Here, we compare serum IgG recognition of Neu5Gc-containing glycoproteins, glycopeptides, and synthetic glycans. First, Neu5Gc-positive or Neu5Gc-deficient mouse strains were used to generate glycopeptides from serum glycoproteins. Then we developed a reproducible ELISA to screen human sera against Neu5Gc-positive glycopeptides for detection of human serum anti-Neu5Gc IgGs. Finally, we evaluated ELISA screens against glycopeptides in comparison with glycoproteins, as well as against elaborated arrays displaying synthetic Neu5Gc-glycans. Our results demonstrate that the presentation mode and diversity of Neu5Gc-glycans are critical for detection of the full collection of human serum anti-Neu5Gc IgGs
Characterization of immunogenic Neu5Gc in bioprosthetic heart valves
Background: The two common sialic acids (Sias) in mammals are N-acetylneuraminic acid (Neu5Ac) and its hydroxylated form N-glycolylneuraminic acid (Neu5Gc). Unlike most mammals, humans cannot synthesize Neu5Gc that is considered foreign and recognized by circulating antibodies. Thus, Neu5Gc is a potential xenogenic carbohydrate antigen in bioprosthetic heart valves (BHV) that tend to deteriorate in time within human patients. Methods: We investigated Neu5Gc expression in non-engineered animal-derived cardiac tissues and in clinically used commercial BHV, and evaluated Neu5Gc immunogenicity on BHV through recognition by human anti-Neu5Gc IgG. Results: Neu5Gc was detected by immunohistochemistry in porcine aortic valves and in porcine and bovine pericardium. Qualitative analysis of Sia linkages revealed Siaa2-3> Siaa2-6 on porcine/bovine pericardium while the opposite in porcine aortic/pulmonary valve cusps. Similarly, six commercial BHV containing either porcine aortic valve or porcine/bovine/equine pericardium revealed Siaa2-3> Siaa2-6 expression. Quantitative analysis of Sia by HPLC showed porcine/bovine pericardium express 4-fold higher Neu5Gc levels compared to the porcine aortic/pulmonary valves, with Neu5Ac at 6-fold over Neu5Gc. Likewise, Neu5Gc was expressed on commercial BHV (186.3 +/- 16.9 pmol Sia/mu g protein), with Neu5Ac at 8-fold over Neu5Gc. Affinity-purified human anti-Neu5Gc IgG showing high specificity toward Neu5Gc-glycans (with no binding to Neu5Ac-glycans) on a glycan microarray, strongly bound to all tested commercial BHV, demonstrating Neu5Gc immune recognition in cardiac xenografts. Conclusions: We conclusively demonstrated Neu5Gc expression in native cardiac tissues, as well as in six commercial BHV. These Neu5Gc xeno-antigens were recognized by human anti-Neu5Gc IgG, supporting their immunogenicity. Altogether, these findings suggest BHV-Neu5Gc/anti-Neu5Gc may play a role in valve deterioration warranting further investigation
Altered somatic hypermutation patterns in COVID-19 patients classifies disease severity
IntroductionThe success of the human body in fighting SARS-CoV2 infection relies on lymphocytes and their antigen receptors. Identifying and characterizing clinically relevant receptors is of utmost importance.MethodsWe report here the application of a machine learning approach, utilizing B cell receptor repertoire sequencing data from severely and mildly infected individuals with SARS-CoV2 compared with uninfected controls.ResultsIn contrast to previous studies, our approach successfully stratifies non-infected from infected individuals, as well as disease level of severity. The features that drive this classification are based on somatic hypermutation patterns, and point to alterations in the somatic hypermutation process in COVID-19 patients.DiscussionThese features may be used to build and adapt therapeutic strategies to COVID-19, in particular to quantitatively assess potential diagnostic and therapeutic antibodies. These results constitute a proof of concept for future epidemiological challenges
Chiral control of current transfer in molecules
Abstract Electron transmission through chiral molecules induced by circularly polarized light can be very different for mirror image structures. This behaviour is described in terms of current transfer: the transfer of both charge and momentum. We review recent theoretical developments on the theory of current transfer and discuss related experimental studies of electron transmission through chiral molecular structures adsorbed on surfaces.
Wastewater-derived contaminants of emerging concern: Concentrations in soil solution under simulated irrigation scenarios
In response to declineing natural water sources, treated wastewater has been introduced into the water cycle as a new water source for irrigation. However, this practice exposes the agricultural environment to various contaminants of emerging concern. To better understand their fate in the soil and to effectively predict their bioavailability for plant uptake, there is a need to quantify their concentrations in soil solutions. In this study, we examined the concentrations of treated wastewater-derived ​contaminants of emerging concern in soil solutions under three scenarios: (1) shifting from irrigation with freshwater to treated wastewater (FW→TWW scenario), (2) long-term continuous irrigation with treated wastewater (TWW→TWW scenario), and (3) prolonged irrigation with treated wastewater followed by freshwater (TWW→FW scenario). Contaminants of emerging concern including carbamazepine, 1H-benzotriazole, lamotrigine, venlafaxine, and thiabendazole were ubiquitous in the treated wastewater (mean concentrations of 125, 945, 180, 3630, and 90 ​ng/L, respectively) and irrigated soils. Interestingly, their concentrations in the soil solutions were different (higher or lower) from the corresponding concentrations in the irrigation water. In both the freshwater to wastewater (FW→TWW) and treated wastewater to freshwater (TWW→FW) irrigation scenarios, lower contaminant concentrations were observed in soil solutions compared to the prolong treated wastewater irrigation scenario (TWW→TWW), indicating that a steady state condition was not achieved after a single irrigation season. For example, the concentrations of 1H-benzotriazole in Nir Oz soil solutions were 638, 310, and 1577 ​ng/L for the three irrigation scenarios, respectively. Moreover, the ​contaminants concentrations in soil solutions were slightly lower in the TWW→FW irrigation scenario compared to the TWW→TWW scenario. Our data suggest that rain-fed crops are also exposed to treated wastewater-derived contaminants of emerging concern released from the adsorbed phase into the soil solution. The readily-available contaminants concentration in soil solution depends on the physicochemical properties of the molecule, the water type used for irrigation and the irrigation history, the contaminant concentration in the irrigation water, and soil characteristics
Tikkoun Sofrim – Combining HTR and Crowdsourcing for Automated Transcription of Hebrew Medieval Manuscripts
Abstract and poster of paper 0568 presented at the Digital Humanities Conference 2019 (DH2019), Utrecht , the Netherlands 9-12 July, 2019
Biomimetic Glyconanoparticle Vaccine for Cancer Immunotherapy
Cancer immunotherapy aims to harness the immune system to combat malignant processes. Transformed cells harbor diverse modifications that lead to formation of neoantigens, including aberrantly expressed cell surface carbohydrates. Targeting tumor-associated carbohydrate antigens (TACA) hold great potential for cancer immunotherapy. N-glycolylneuraminic acid (Neu5Gc) is a dietary non-human immunogenic carbohydrate that accumulates on human cancer cells, thereby generating neoantigens. In mice, passive immunotherapy with anti-Neu5Gc antibodies inhibits growth of Neu5Gc-positive tumors. Here, we designed an active cancer vaccine immunotherapy strategy to target Neu5Gc-positive tumors. We generated biomimetic glyconanoparticles using engineered αGal knockout porcine red blood cells to form nanoghosts (NGs) that either express (NGpos) or lack expression (NGneg) of Neu5Gc-glycoconjugates in their natural context. We demonstrated that optimized immunization of "human-like" Neu5Gc-deficient Cmah-/- mice with NGpos glyconanoparticles induce a strong, diverse and persistent anti-Neu5Gc IgG immune response. The resulting anti-Neu5Gc IgG antibodies were also detected within Neu5Gc-positive tumors and inhibited tumor growth in vivo. Using detailed glycan microarray analysis, we further demonstrate that the kinetics and quality of the immune responses influence the efficacy of the vaccine. These findings reinforce the potential of TACA neoantigens and the dietary non-human sialic acid Neu5Gc, in particular, as immunotherapy targets
Characterization of immunogenic Neu5Gc in bioprosthetic heart valves
Background: The two common sialic acids (Sias) in mammals are N-acetylneuraminic acid (Neu5Ac) and its hydroxylated form N-glycolylneuraminic acid (Neu5Gc). Unlike most mammals, humans cannot synthesize Neu5Gc that is considered foreign and recognized by circulating antibodies. Thus, Neu5Gc is a potential xenogenic carbohydrate antigen in bioprosthetic heart valves (BHV) that tend to deteriorate in time within human patients. Methods: We investigated Neu5Gc expression in non-engineered animal-derived cardiac tissues and in clinically used commercial BHV, and evaluated Neu5Gc immunogenicity on BHV through recognition by human anti-Neu5Gc IgG. Results: Neu5Gc was detected by immunohistochemistry in porcine aortic valves and in porcine and bovine pericardium. Qualitative analysis of Sia linkages revealed Siaa2-3> Siaa2-6 on porcine/bovine pericardium while the opposite in porcine aortic/pulmonary valve cusps. Similarly, six commercial BHV containing either porcine aortic valve or porcine/bovine/equine pericardium revealed Siaa2-3> Siaa2-6 expression. Quantitative analysis of Sia by HPLC showed porcine/bovine pericardium express 4-fold higher Neu5Gc levels compared to the porcine aortic/pulmonary valves, with Neu5Ac at 6-fold over Neu5Gc. Likewise, Neu5Gc was expressed on commercial BHV (186.3 +/- 16.9 pmol Sia/mu g protein), with Neu5Ac at 8-fold over Neu5Gc. Affinity-purified human anti-Neu5Gc IgG showing high specificity toward Neu5Gc-glycans (with no binding to Neu5Ac-glycans) on a glycan microarray, strongly bound to all tested commercial BHV, demonstrating Neu5Gc immune recognition in cardiac xenografts. Conclusions: We conclusively demonstrated Neu5Gc expression in native cardiac tissues, as well as in six commercial BHV. These Neu5Gc xeno-antigens were recognized by human anti-Neu5Gc IgG, supporting their immunogenicity. Altogether, these findings suggest BHV-Neu5Gc/anti-Neu5Gc may play a role in valve deterioration warranting further investigation