Combined protein construct and synthetic gene engineering for heterologous protein expression and crystallization using Gene Composer

<p>Abstract</p> <p>Background</p> <p>With the goal of improving yield and success rates of heterologous protein production for structural studies we have developed the database and algorithm software package Gene Composer. This freely available electronic tool facilitates the information-rich design of protein constructs and their engineered synthetic gene sequences, as detailed in the accompanying manuscript.</p> <p>Results</p> <p>In this report, we compare heterologous protein expression levels from native sequences to that of codon engineered synthetic gene constructs designed by Gene Composer. A test set of proteins including a human kinase (P38α), viral polymerase (HCV NS5B), and bacterial structural protein (FtsZ) were expressed in both <it>E. coli </it>and a cell-free wheat germ translation system. We also compare the protein expression levels in <it>E. coli </it>for a set of 11 different proteins with greatly varied G:C content and codon bias.</p> <p>Conclusion</p> <p>The results consistently demonstrate that protein yields from codon engineered Gene Composer designs are as good as or better than those achieved from the synonymous native genes. Moreover, structure guided N- and C-terminal deletion constructs designed with the aid of Gene Composer can lead to greater success in gene to structure work as exemplified by the X-ray crystallographic structure determination of FtsZ from <it>Bacillus subtilis</it>. These results validate the Gene Composer algorithms, and suggest that using a combination of synthetic gene and protein construct engineering tools can improve the economics of gene to structure research.</p

Perceived contributions of multifunctional landscapes to human well-being : Evidence from 13 European sites

Multifunctional landscapes provide critical benefits and are essential for human well-being. The relationship between multifunctional landscapes and well-being has mostly been studied using ecosystem services as a linkage. However, there is a challenge of concretizing what human well-being exactly is and how it can be measured, particularly in relation to ecosystem services, landscape values and related discussions. In this paper, we measure self-reported well-being through applying an inductive free-listing approach to the exploration of the relationships between landscape multifunctionality and human well-being across 13 rural and peri-urban sites in Europe. We developed a face-to-face online survey (n = 2,301 respondents) integrating subjective perceptions of well-being (free-listing method) with mapping perceived ecosystem service benefits (Public Participation GIS, PPGIS approach). Applying content analysis and diverse statistical methods, we explore the links between well-being (i.e. perceived well-being items such as tranquillity, social relations and health) and social-ecological properties (i.e. respondents' sociocultural characteristics and perception of ecosystem service benefits). We identify 40 different well-being items highlighting prominently landscape values. The items form five distinct clusters: access to services; tranquillity and social capital; health and nature; cultural landscapes; and place attachment. Each cluster is related to specific study sites and explained by certain social-ecological properties. Results of our inductive approach further specify pre-defined conceptualizations on well-being and their connections to the natural environment. Results suggest that the well-being contributions of multifunctional landscapes are connected to therapeutic well-being effects, which are largely neglected in the ecosystem services literature. Our results further point to the context-specific character of linkages between landscapes and human well-being. The clusters highlight that landscape-supported well-being is related to multiple interlinked items that can inform collective visions of well-being in the future. For landscape planning and management, we highlight the need for place-specific analysis and consideration of perceptions of local people to identify the contributions to their well-being. Future research would benefit from considering the experiential qualities of value and well-being as they relate to direct experiences with the landscape and wider psychological needs, specifically over time. A free Plain Language Summary can be found within the Supporting Information of this article.Peer reviewe

Formation and evolution of the ionospheric plasma density shoulder and its relationship to the superfountain effects investigated during the 6 November 2001 great storm

This study investigates the 6 November 2001 great storm’s impact on the topside ionosphere utilizing data from the onboard TOPEX/Poseidon-NASA altimeter, Defense Meteorological Satellite Program–Special Sensor Ions, Electrons and Scintillation instruments and ACE interplanetary observatory. A set of field-aligned profiles demonstrate the storm evolution, caused by the precursor and promptly penetrating interplanetary eastward electric (E) fields, and strong equatorward winds reducing chemical loss, during the long-duration negative BZ events. At daytime-evening, the forward fountain experienced repeated strengthening, as the net eastward E field suddenly increased. The resultant symmetrical equatorial anomaly exhibited a continuous increase,while the energy inputs at both auroral regions were similar. In both hemispheres, by progressing poleward, a midlatitude shoulder exhibiting increased plasma densities, a plasma-density dropoff (steep gradient) and a plasma depletion appeared. These features were maintained while the reverse fountain operated. At the dropoff, elevated temperatures indicated the plasmapause. Consequently, the plasma depletion was the signature of plasmaspheric erosion. In each hemisphere, an isolated plasma flow, supplying the minimum plasma, was detected at the shoulder. Plasmaspheric compression, due to the enhanced E fields, could trigger this plasma flow. Exhibiting strong longitudinal variation at evening-nighttime, the shoulder increased 306% over the southeastern Pacific, where the nighttime Weddell Sea Anomaly (WSA) appeared before the storm. There, the shoulder indicated the storm-enhanced equatorward section of the quiet time WSA. Owing to the substantial equatorward plasmapause movement, a larger poleward section of the quiet time WSA eroded away, leaving a large depletion behind. This study reports first these (northern, southern) plasma flows and dramatic storm effects on a nighttime WSA

Dynamic genome evolution in a model fern

The large size and complexity of most fern genomes have hampered efforts to elucidate fundamental aspects of fern biology and land plant evolution through genome-enabled research. Here we present a chromosomal genome assembly and associated methylome, transcriptome and metabolome analyses for the model fern species Ceratopteris richardii. The assembly reveals a history of remarkably dynamic genome evolution including rapid changes in genome content and structure following the most recent whole-genome duplication approximately 60 million years ago. These changes include massive gene loss, rampant tandem duplications and multiple horizontal gene transfers from bacteria, contributing to the diversification of defence-related gene families. The insertion of transposable elements into introns has led to the large size of the Ceratopteris genome and to exceptionally long genes relative to other plants. Gene family analyses indicate that genes directing seed development were co-opted from those controlling the development of fern sporangia, providing insights into seed plant evolution. Our findings and annotated genome assembly extend the utility of Ceratopteris as a model for investigating and teaching plant biology

Rationalization and Design of the Complementarity Determining Region Sequences in an Antibody-Antigen Recognition Interface

Protein-protein interactions are critical determinants in biological systems. Engineered proteins binding to specific areas on protein surfaces could lead to therapeutics or diagnostics for treating diseases in humans. But designing epitope-specific protein-protein interactions with computational atomistic interaction free energy remains a difficult challenge. Here we show that, with the antibody-VEGF (vascular endothelial growth factor) interaction as a model system, the experimentally observed amino acid preferences in the antibody-antigen interface can be rationalized with 3-dimensional distributions of interacting atoms derived from the database of protein structures. Machine learning models established on the rationalization can be generalized to design amino acid preferences in antibody-antigen interfaces, for which the experimental validations are tractable with current high throughput synthetic antibody display technologies. Leave-one-out cross validation on the benchmark system yielded the accuracy, precision, recall (sensitivity) and specificity of the overall binary predictions to be 0.69, 0.45, 0.63, and 0.71 respectively, and the overall Matthews correlation coefficient of the 20 amino acid types in the 24 interface CDR positions was 0.312. The structure-based computational antibody design methodology was further tested with other antibodies binding to VEGF. The results indicate that the methodology could provide alternatives to the current antibody technologies based on animal immune systems in engineering therapeutic and diagnostic antibodies against predetermined antigen epitopes

Doxycycline versus prednisolone as an initial treatment strategy for bullous pemphigoid: a pragmatic non-inferiority randomised controlled trial

Background: Bullous pemphigoid (BP) is a blistering skin disorder with increased mortality. We tested whether a strategy of starting treatment with doxycycline conveys acceptable short-term blister control whilst conferring long-term safety advantages over starting treatment with oral corticosteroids. Methods: Pragmatic multi-centre parallel-group randomised controlled trial of adults with BP (≥3 blisters ≥2 sites and linear basement membrane IgG/C3) plus economic evaluation. Participants were randomised to doxycycline (200 mg/day) or prednisolone (0·5 mg/kg/day). Localised adjuvant potent topical corticosteroids (<30 g/week) was permitted weeks 1-3. The non-inferiority primary effectiveness outcome was the proportion of participants with ≤3 blisters at 6 weeks. We assumed that doxycycline would be 25% less effective than corticosteroids with a 37% acceptable margin of noninferiority. The primary safety outcome was the proportion with severe, life-threatening or fatal treatment-related adverse events by 52 weeks. Analysis used a regression model adjusting for baseline disease severity, age and Karnofsky score, with missing data imputed. Results: 132 patients were randomised to doxycycline and 121 to prednisolone from 54 UK and 7 German dermatology centres. Mean age was 77·7 years and 68.4% had moderate to severe baseline disease. For those starting doxycycline, 83/112 (74·1%) had ≤3 blisters at 6 weeks compared with 92/101 (91·1%) for prednisolone, a difference of 18·6% favouring prednisolone (upper limit of 90% CI, 26·1%, within the predefined 37% margin). Related severe, life-threatening and fatal events at 52 weeks were 18·5% for those starting doxycycline and 36·6% for prednisolone (mITT analysis), an adjusted difference of 19·0% (95% CI, 7·9%, 30·1%, p=0·001). Conclusions: A strategy of starting BP patients on doxycycline is non-inferior to standard treatment with oral prednisolone for short-term blister control and significantly safer long-term

Basic science232. Certolizumab pegol prevents pro-inflammatory alterations in endothelial cell function

Background: Cardiovascular disease is a major comorbidity of rheumatoid arthritis (RA) and a leading cause of death. Chronic systemic inflammation involving tumour necrosis factor alpha (TNF) could contribute to endothelial activation and atherogenesis. A number of anti-TNF therapies are in current use for the treatment of RA, including certolizumab pegol (CZP), (Cimzia ®; UCB, Belgium). Anti-TNF therapy has been associated with reduced clinical cardiovascular disease risk and ameliorated vascular function in RA patients. However, the specific effects of TNF inhibitors on endothelial cell function are largely unknown. Our aim was to investigate the mechanisms underpinning CZP effects on TNF-activated human endothelial cells. Methods: Human aortic endothelial cells (HAoECs) were cultured in vitro and exposed to a) TNF alone, b) TNF plus CZP, or c) neither agent. Microarray analysis was used to examine the transcriptional profile of cells treated for 6 hrs and quantitative polymerase chain reaction (qPCR) analysed gene expression at 1, 3, 6 and 24 hrs. NF-κB localization and IκB degradation were investigated using immunocytochemistry, high content analysis and western blotting. Flow cytometry was conducted to detect microparticle release from HAoECs. Results: Transcriptional profiling revealed that while TNF alone had strong effects on endothelial gene expression, TNF and CZP in combination produced a global gene expression pattern similar to untreated control. The two most highly up-regulated genes in response to TNF treatment were adhesion molecules E-selectin and VCAM-1 (q 0.2 compared to control; p > 0.05 compared to TNF alone). The NF-κB pathway was confirmed as a downstream target of TNF-induced HAoEC activation, via nuclear translocation of NF-κB and degradation of IκB, effects which were abolished by treatment with CZP. In addition, flow cytometry detected an increased production of endothelial microparticles in TNF-activated HAoECs, which was prevented by treatment with CZP. Conclusions: We have found at a cellular level that a clinically available TNF inhibitor, CZP reduces the expression of adhesion molecule expression, and prevents TNF-induced activation of the NF-κB pathway. Furthermore, CZP prevents the production of microparticles by activated endothelial cells. This could be central to the prevention of inflammatory environments underlying these conditions and measurement of microparticles has potential as a novel prognostic marker for future cardiovascular events in this patient group. Disclosure statement: Y.A. received a research grant from UCB. I.B. received a research grant from UCB. S.H. received a research grant from UCB. All other authors have declared no conflicts of interes

Multidifferential study of identified charged hadron distributions in ZZ-tagged jets in proton-proton collisions at s=\sqrt{s}=13 TeV

Jet fragmentation functions are measured for the first time in proton-proton collisions for charged pions, kaons, and protons within jets recoiling against a $Z$ boson. The charged-hadron distributions are studied longitudinally and transversely to the jet direction for jets with transverse momentum 20 $< p_{\textrm{T}} < 100$ GeV and in the pseudorapidity range $2.5 < \eta < 4$. The data sample was collected with the LHCb experiment at a center-of-mass energy of 13 TeV, corresponding to an integrated luminosity of 1.64 fb$^{-1}$. Triple differential distributions as a function of the hadron longitudinal momentum fraction, hadron transverse momentum, and jet transverse momentum are also measured for the first time. This helps constrain transverse-momentum-dependent fragmentation functions. Differences in the shapes and magnitudes of the measured distributions for the different hadron species provide insights into the hadronization process for jets predominantly initiated by light quarks.Comment: All figures and tables, along with machine-readable versions and any supplementary material and additional information, are available at https://cern.ch/lhcbproject/Publications/p/LHCb-PAPER-2022-013.html (LHCb public pages