Search Results - "Drake, Penelope M"
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Sweetening the Pot: Adding Glycosylation to the Biomarker Discovery Equation
Published in Clinical chemistry (Baltimore, Md.) (01-02-2010)“…Cancer has profound effects on gene expression, including a cell's glycosylation machinery. Thus, tumors produce glycoproteins that carry oligosaccharides with…”
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Maytansine-bearing antibody-drug conjugates induce in vitro hallmarks of immunogenic cell death selectively in antigen-positive target cells
Published in Oncoimmunology (01-01-2019)“…Oncology treatment has been revolutionized by the introduction of immune checkpoint inhibitor drugs, which enable 20-40% of patients to generate anti-tumor…”
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Recent Developments in ADC Technology: Preclinical Studies Signal Future Clinical Trends
Published in BioDrugs : clinical immunotherapeutics, biopharmaceuticals, and gene therapy (01-12-2017)“…The antibody–drug conjugate (ADC) field is in a transitional period. Older approaches to conjugate composition and dosing regimens still dominate the ADC…”
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Polysialic acid enhances the migration and invasion of human cytotrophoblasts
Published in Glycobiology (Oxford) (01-05-2013)“…Polysialic acid (polySia) is a large, cell-surface linear homopolymer composed of α2,8-linked sialic acid residues. Most extensively studied in the nervous…”
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A lectin affinity workflow targeting glycosite-specific, cancer-related carbohydrate structures in trypsin-digested human plasma
Published in Analytical biochemistry (2011)“…Glycans are cell-type-specific, posttranslational protein modifications that are modulated during developmental and disease processes. As such, glycoproteins…”
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Antibody-Drug Conjugates Targeting the Urokinase Receptor (uPAR) as a Possible Treatment of Aggressive Breast Cancer
Published in Antibodies (Basel) (05-11-2019)“…A promising molecular target for aggressive cancers is the urokinase receptor (uPAR). A fully human, recombinant antibody that binds uPAR to form a stable…”
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An emerging playbook for antibody–drug conjugates: lessons from the laboratory and clinic suggest a strategy for improving efficacy and safety
Published in Current opinion in chemical biology (01-10-2015)“…•Review of current challenges facing ADC development.•Examine relationship between ADC composition and function.•Opportunities for ADC innovation and future…”
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Polysialic Acid Governs T-Cell Development by Regulating Progenitor Access to the Thymus
Published in Proceedings of the National Academy of Sciences - PNAS (21-07-2009)“…Although the polysialyltransferase ST8Sia IV is expressed in both primary and secondary human lymphoid organs, its product, polysialic acid (polySia), has been…”
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Tandem-Cleavage Linkers Improve the In Vivo Stability and Tolerability of Antibody–Drug Conjugates
Published in Bioconjugate chemistry (21-04-2021)“…Although peptide motifs represent the majority of cleavable linkers used in clinical-stage antibody–drug conjugates (ADCs), the sequences are often sensitive…”
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Aldehyde Tag Coupled with HIPS Chemistry Enables the Production of ADCs Conjugated Site-Specifically to Different Antibody Regions with Distinct in Vivo Efficacy and PK Outcomes
Published in Bioconjugate chemistry (16-07-2014)“…It is becoming increasingly clear that site-specific conjugation offers significant advantages over conventional conjugation chemistries used to make…”
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Human pregnancy: the role of chemokine networks at the fetal-maternal interface
Published in Expert reviews in molecular medicine (10-05-2004)“…Chemokines are multifunctional molecules initially described as having a role in leukocyte trafficking and later found to participate in developmental…”
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Reciprocal chemokine receptor and ligand expression in the human placenta: Implications for cytotrophoblast differentiation
Published in Developmental dynamics (01-04-2004)“…At the onset of pregnancy, the human placenta, which forms the interface between the embryo/fetus and the mother, must rapidly develop into a life‐sustaining…”
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Hydrazino-Pictet-Spengler Ligation as a Biocompatible Method for the Generation of Stable Protein Conjugates
Published in Bioconjugate chemistry (19-06-2013)“…Aldehyde- and ketone-functionalized biomolecules have found widespread use in biochemical and biotechnological fields. They are typically conjugated with…”
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A Case Study to Identify the Drug Conjugation Site of a Site-Specific Antibody-Drug-Conjugate Using Middle-Down Mass Spectrometry
Published in Journal of the American Society for Mass Spectrometry (01-11-2019)“…Middle-down mass spectrometry (MD MS) has emerged as a promising alternative to classical bottom-up approaches for protein characterization. Middle-level…”
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IDPicker 2.0: Improved Protein Assembly with High Discrimination Peptide Identification Filtering
Published in Journal of proteome research (01-08-2009)“…Tandem mass spectrometry-based shotgun proteomics has become a widespread technology for analyzing complex protein mixtures. A number of database searching…”
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Reconstitution of Formylglycine-generating Enzyme with Copper(II) for Aldehyde Tag Conversion
Published in The Journal of biological chemistry (19-06-2015)“…To further our aim of synthesizing aldehyde-tagged proteins for research and biotechnology applications, we developed methods for recombinant production of…”
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Reversal of gene dysregulation in cultured cytotrophoblasts reveals possible causes of preeclampsia
Published in The Journal of clinical investigation (01-07-2013)“…During human pregnancy, a subset of placental cytotrophoblasts (CTBs) differentiates into cells that aggressively invade the uterus and its vasculature,…”
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A Novel HER2-targeted Antibody–drug Conjugate Offers the Possibility of Clinical Dosing at Trastuzumab-equivalent Exposure Levels
Published in Molecular cancer therapeutics (01-09-2020)“…Abstract Trastuzumab and the related ADC, ado-trastuzumab emtansine (T-DM1), both target HER2-overexpressing cells. Together, these drugs have treatment…”
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Insights from native mass spectrometry approaches for top- and middle- level characterization of site-specific antibody-drug conjugates
Published in mAbs (04-07-2017)“…Antibody-drug conjugates (ADCs) have emerged as a family of compounds with promise as efficient immunotherapies. First-generation ADCs were generated mostly…”
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A simple LC/MRM–MS-based method to quantify free linker-payload in antibody-drug conjugate preparations
Published in Journal of chromatography. B, Analytical technologies in the biomedical and life sciences (01-10-2016)“…•A simple MRM-based method to quantify free linker-payload in an ADC is described.•The approach has an LLOQ of 10nM and requires no special laboratory…”
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