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Glycosylation is a topic of intense current interest in the development of biopharmaceuticals because it is related to drug safety and efficacy. This work describes results of an interlaboratory study on the glycosylation of the Primary Sample (PS) of NISTmAb, a monoclonal antibody reference material. Seventy-six laboratories from industry, university, research, government, and hospital sectors in Europe, North America, Asia, and Australia submitted a total of 103 reports on glycan distributions. The principal objective of this study was to report and compare results for the full range of analytical methods presently used in the glycosylation analysis of mAbs. Therefore, participation was unrestricted, with laboratories choosing their own measurement techniques. Protein glycosylation was determined in various ways, including at the level of intact mAb, protein fragments, glycopeptides, or released glycans, using a wide variety of methods for derivatization, separation, identification, and quantification. Consequently, the diversity of results was enormous, with the number of glycan compositions identified by each laboratory ranging from 4 to 48. In total, one hundred sixteen glycan compositions were reported, of which 57 compositions could be assigned consensus abundance values. These consensus medians provide community-derived values for NISTmAb PS. Agreement with the consensus medians did not depend on the specific method or laboratory type. The study provides a view of the current state-of-the-art for biologic glycosylation measurement and suggests a clear need for harmonization of glycosylation analysis methods.

Utilizing imaging spectroscopy technology to identify methane super‐emitters plays a vital role in mitigating methane emissions in the Oil & Gas (O&G) sector. While earlier research has uncovered significant point‐source methane emissions from O&G production in the US and Canada, which are key regions with large methane emissions, a comprehensive post‐COVID‐19 survey has been notably absent. Here, we perform a detailed survey of methane super‐emitters across multiple basins of North America (Marcellus Shale, Haynesville/Bossier Shale, Permian Basin and Montney Shale) using the new Chinese Gaofen5‐01A/02 (GF5‐01A/02) satellite measurements during 2022–2023. We detect 139 individual methane plumes emanating from 122 point sources, with flux rates ranging from 519 to 16,071 kg hr−1. These emissions exhibit a highly skewed and heavy‐tailed distribution, constituting approximately 23% of the flux inversion with TROPOMI in the sample region, with a range of 13%–40%. Moreover, we observe a 66.7% reduction in methane emissions in Permian Basin during COVID‐19, followed by fluctuations until spring 2023. By summer 2023, methane emissions rebound to twice their previous magnitude (1.68 ± 0.58 Tg a−1). Using these point‐source surveys, we further quantify a regional methane emission of 2.69 ± 0.86 Tg a−1 in Permian Basin. This estimation closely aligns with top‐down inversions (2.22 ± 0.40 Tg a−1) from TROPOMI. The upscale estimation underscores the effectiveness of high‐resolution remote sensing measurements in improving bottom‐up emissions inventories and refining regional methane emission assessments. Our results highlight the potential climate benefits derived from regular monitoring and specific remediation efforts focused on relatively few strong point‐source emissions. Plain Language Summary: Reducing methane (CH4) leaks from Oil & Gas (O&G) production is crucial for abating climate change. However, detecting these abnormal CH4 emissions globally is challenging as they often occur unexpectedly. Satellite remote sensing with hyperspectral imaging spectrometer provides an effective approach for top‐down monitoring. These instruments produce CH4 plume maps, enabling the quantification of emissions. In this research, we conduct a comprehensive survey in major O&G basins of North America during 2022–2023 using the new Chinese Gaofen5‐01A/02 satellite. Through repeated observations by high‐resolution satellites, we capture CH4 emission dynamics in sample basins and quantify their contribution to regional methane budget. Our results demonstrate the value of high‐resolution satellite observations in reducing uncertainties in quantifying anthropogenic CH4 emission and supporting strategies for emission mitigation. Key Points: The new Chinese Gaofen5‐01A/02 hyperspectral satellite missions have great capability in methane mappingWe find substantial methane point‐source emissions in Permian Basin after COVID‐19 during 2022–2023Satellite‐based survey can effectively improve bottom‐up regional methane emissions inventories [ABSTRACT FROM AUTHOR]

Motivation Molecular representation learning is pivotal for advancing deep learning applications in quantum chemistry and drug discovery. Existing methods for molecular representation learning often fall short of fully capturing the intricate interactions within chemical bonds of 2D topological graphs and the multifaceted effects of 3D geometric conformations. Results To overcome these challenges, we present a novel contrastive learning strategy for molecular representation learning, named G eometric T riangle A wareness M odel (GTAM). This method integrates innovative molecular encoders for both 2D graphs and 3D conformations, enabling the accurate capture of geometric dependencies among edges in graph-based molecular structures. Furthermore, GTAM is bolstered by the development of two contrastive training objectives designed to facilitate the direct transfer of edge information between 2D topological graphs and 3D geometric conformations, enhancing the functionality of the molecular encoders. Through extensive evaluations on a range of 2D and 3D downstream tasks, our model has demonstrated superior performance over existing approaches. Availability and implementation The test code and data of GTAM are available online at https://github.com/StellaHxy/GTAM. [ABSTRACT FROM AUTHOR]