Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Jennifer L. Lippens"'
Publikováno v:
Journal of Cheminformatics, Vol 16, Iss 1, Pp 1-14 (2024)
Abstract Small molecule identification is a crucial task in analytical chemistry and life sciences. One of the most commonly used technologies to elucidate small molecule structures is mass spectrometry. Spectral library search of product ion spectra
Externí odkaz:
https://doaj.org/article/73ad185aefad4f4d9acc13963584d7e1
Autor:
Youzhong Liu, Yingjie Zhang, Tom Vennekens, Jennifer L. Lippens, Luc Duijsens, Danh Bui-Thi, Kris Laukens, Thomas de Vijlder
Publikováno v:
Analytical chemistry
Small molecule structure elucidation using tandem mass spectrometry (MS/MS) plays a crucial role in life science, bioanalytical, and pharmaceutical research. There is a pressing need for increased throughput of compound identification and transformat
Autor:
Iain D. G. Campuzano, Emma M. Pelegri-O’Day, Nithya Srinivasan, Jennifer L. Lippens, Pascal Egea, Aiko Umeda, Jennifer Aral, Tianqi Zhang, Arthur Laganowsky, Chawita Netirojjanakul
Publikováno v:
Journal of the American Society for Mass Spectrometry. 33(11)
Reversed-phase liquid chromatographic mass spectrometry (rpLC-MS) is a universal, platformed, and essential analytical technique within pharmaceutical and biopharmaceutical research. Typical rpLC method gradient times can range from 5 to 20 min. As m
Autor:
John O. Hui, Stone D.-H. Shi, Pascal F. Egea, John H. Robinson, Jennifer L. Lippens, Michael Nshanian, Dhanashri Bagal, Joseph A. Loo, Marshall Bern, Chawita Netirojjanakul, Iain D. G. Campuzano
Publikováno v:
Analytical chemistry, vol 91, iss 15
Anal Chem
Anal Chem
Electrospray ionization mass spectrometry (ESI-MS) is a ubiquitously used analytical method applied across multiple departments in biopharma, ranging from early research discovery to process development. Accurate, efficient, and consistent protein MS
Autor:
Iain D. G. Campuzano, Pascal F. Egea, James E. Keener, Amit Vaish, Michael T. Marty, Joseph A. Loo, Jennifer L. Lippens, Chris Spahr
Publikováno v:
Analytical Chemistry. 90:13616-13623
Therapeutic target characterization involves many components, including accurate molecular weight (MW) determination. Knowledge of the accurate MW allows one to detect the presence of post-translational modifications, proteolytic cleavages, and impor
Autor:
Steven L. Van Orden, Iain Campuzano, Joseph A. Loo, Jennifer L. Lippens, Michael Nshanian, Chawita Netirojjanakul, David P. A. Kilgour
Publikováno v:
Analytical Chemistry. 90:745-751
Antibody drug conjugates (ADCs) are an important class of therapeutic molecule currently being used to treat HER2-positive metastatic breast cancer, relapsed or refractory Hodgkin lymphoma, systemic anaplastic large cell lymphoma, relapsed or refract
Autor:
Juraj Svitel, Han Xu, Jennifer L. Lippens, Joseph A. Loo, Robert J. M. Kurzeja, Iain Campuzano, Dhanashri Bagal, Paul D. Schnier, Huilin Li
Publikováno v:
Analytical Chemistry. 88:12427-12436
Over the past two decades orthogonal acceleration time-of-flight has been the de facto analyzer of choice for solution and membrane soluble protein native mass spectrometry (MS) studies; this however is gradually changing. Here we compare three MS in
Autor:
Richa Sarin, Antonius Koller, Ziqing Lin, Luis F. Schachner, Wonhyeuk Jung, Lloyd M. Smith, Ljiljana Paša-Tolić, Julia Chamot-Rooke, Alexander R. Ivanov, Iain D. G. Campuzano, Carter Lantz, Ying Ge, Caroline J. DeHart, Julian P. Whitelegge, Jennifer L. Lippens, Kendall Johnson, Krishna Aluri, Catherine M. Rawlins, Yury O. Tsybin, Neil L. Kelleher, Jeffrey N. Agar, Paul O. Danis, Daniel P. Donnelly, Jared R. Auclair, Jeremy J. Wolff, Joseph A. Loo, Luca Fornelli, Bifan Chen
Publikováno v:
Nature methods, vol 16, iss 7
Nature Methods
Nature Methods, Nature Publishing Group, 2019, 16 (7), pp.587-594. ⟨10.1038/s41592-019-0457-0⟩
Nature Methods, 2019, 16 (7), pp.587-594. ⟨10.1038/s41592-019-0457-0⟩
Nature Methods
Nature Methods, Nature Publishing Group, 2019, 16 (7), pp.587-594. ⟨10.1038/s41592-019-0457-0⟩
Nature Methods, 2019, 16 (7), pp.587-594. ⟨10.1038/s41592-019-0457-0⟩
One gene can give rise to many functionally distinct proteoforms, each of which has a characteristic molecular mass. Top-down mass spectrometry enables the analysis of intact proteins and proteoforms. Here members of the Consortium for Top-Down Prote
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f4d2ff753f4535711f739a1916ff31f
https://escholarship.org/uc/item/72c7s81j
https://escholarship.org/uc/item/72c7s81j
Publikováno v:
Rapid Communications in Mass Spectrometry. 30:773-783
RATIONALE The observation of intact non-covalent complexes by electrospray ionization mass spectrometry (ESI-MS) hinges on the ability to minimize in-source activation processes that take place during analyte desolvation. We explored the merits of re
Publikováno v:
The Analyst. 141:4084-4099
This study explored the use of modular nucleic acid (NA) standards to generate calibration curves capable of translating primary ion mobility readouts into corresponding collision cross section (CCS) data. Putative calibrants consisted of single- (ss