Downstream Processing of Cell Culture-Derived Animal Viruses
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Calcium Lability of Cytoplasmic Microtubules and Its Modulation By
Proc. Natl. Acad. Sci. USA Vol. 78, No. 2, pp. 1037-1041, February 1981 Cell Biology Calcium lability of cytoplasmic microtubules and its modulation by microtubule-associated proteins (detergent extraction/calmodulin/calmodulin inhibitors/immunofluorescence microscopy) MANFRED SCHLIWA*, URSULA EUTENEUER*, JEANNETTE CHLOE BULINSKItt, AND JONATHAN G. IZANT* *Department of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, Colorado 80309; and tLaboratory of Molecular Biology, University of Wisconsin, Madison, Wisconsin 53706 Communicated by Keith R. Porter, October 31, 1980 ABSTRACT Detergent-extracted BSC-1 monkey cells have The discovery that calmodulin, a ubiquitous Ca2+-binding been used as a model system to study the Ca2+ sensitivity of in vivo protein that regulates a number of Ca2+-dependent functions polymerized microtubules under in vitro conditions. The effects (for reviews, see refs. 9 and 10), influences microtubule assem- of various experimental treatments were observed by immuno- has the fluorescence microscopy. Whereas microtubules are completely bly in vitro in a Ca2+-dependent manner (11) opened stable at Ca2+ concentrations below 1 pM, Ca2+ at greater than possibility that Ca2+ effects on microtubules are mediated by 1-4 ,uM induces microtubule disassembly that begins in the cell this protein. Immunofluorescence microscopy with antibodies periphery and proceeds towards the cell center. At concentrations against calmodulin further showed an association of this protein of up to 500 jiM, both the pattern and time course of disassembly with certain components of the mitotic spindle (12, 13), sug- are not markedly altered, suggesting that, within this concentra- gesting an important role in Ca2+-dependent functions during tion range, Ca2+ effects are catalytic rather than stoichiometric. -
Purification of Recombinant Vaccinia Virus for Oncolytic and Immunotherapeutic Applications Using Monolithic Column Technology
Purification of Recombinant Vaccinia Virus for Oncolytic and Immunotherapeutic Applications using Monolithic Column Technology A thesis submitted to University College London for the degree of Doctor of Engineering by David Isaac William Vincent The Advanced Centre for Biochemical Engineering Department of Biochemical Engineering University College London Gordon Street London WC1H 0AH 1 I, David Vincent confirm that the work presented in this thesis is my own. Where information has been derived from other sources, I confirm that this has been indicated in the thesis. Signed……………….………………………Date……………………………………… 2 Acknowledgements I would like to thank my supervisor Dr Yuhong Zhou for her invaluable feedback and support over the course of this EngD. Without her continuous encouragement this work would likely never have been completed. I would also like to thank my Advisor Prof. Ajoy Velayudhan for his help and guidance. Many a long discussion was had on the intricacies of vaccinia viral purification which were thought provoking, inspirational but also really good fun. I would also like to express my gratitude to the staff and students at UCL. There are too many to mention everyone, but in particular I would like to thank Mrs Ludmila Ruban, Miss Dhushy Stanislaus and Dr Tarit Mukhopadhyay for their support, especially in setting up the vaccine lab in the department which I could benefit from in my final year. I would also like to thank Dr Patricia Perez Esteban for her support, friendship and bioprocess wisdom. I would like to express my gratitude to BIA Separations and the EPSRC for sponsoring this work. Without this financial support this work would not have been possible. -
Molecules Involved in Proliferation of Normal and Cancer Cells: Presidential Address1
[CANCER RESEARCH 47. 1488-1491, March 15, 1987] Molecules Involved in Proliferation of Normal and Cancer Cells: Presidential Address1 Arthur B. Pardee Division of Cell Growth and Regulation, Dana-Farber Cancer Institute, Boston, Massachusetts 02115 Overview may permit the escape of cells from growth control. The proposal that a labile protein is necessary for prolifera All definitions of cancer stress the defective regulation of cell tion of normal cells and that its levels are altered in tumorigenic growth and differentiation because such physiological aberra cells led us to examine proteins on two-dimensional gels. A tions underlie the gross derangements of the disease. An im candidate protein which was unstable in normal cells but rela portant goal of basic cancer biology is to provide molecular tively stabilized in tumorigenic cells was indeed identified. It explanations for these defective cellular processes. With recent has been shown to possess a molecular weight of 68,000. This developments in molecular and cellular biology, investigators protein is one of a very small number closely linked to cell have obtained penetrating insights into cell processes and their proliferation during G|. Our work in progress is designed to respective derangements. These are being investigated at four further identify this protein, clone its gene, and study its prop experimental levels: genes and their mRNAs; growth factors erties in normal cells that have been transfected with this gene. and their receptors; biochemical regulation; and cell biology in We are also investigating events following the restriction culture. The results are interrelated and integrated within the point. The rather long time interval (about 2 h) between the framework of the classical cell proliferation cycle. -
BIA Separations CIM Monolithic Columns for Purification and Analytics of Biomolecules
BIA Separations CIM Monolithic Columns for Purification and Analytics of Biomolecules Lidija Urbas, PhD [email protected] Outline • BIA Separations • Chromatography – Monolithic Chromatography – Design of monolithic columns • DSP applications • PAT columns and applications: – Case study: combining DSP and PAT of Adenoviruses • Conclusions Ajdovščina BIA Separations • BIA Separations was founded in September 1998. • Headquarters in Austria, R&D and Production in Slovenia. BIA Separations • BIA Separations was founded in September 1998. • Headquarters in Austria, R&D and Production in Slovenia. • BIA Separations USA established in September 2007 - sales and tech support office. • BIA Separations China established in January 2011 - sales and tech support office. • 90 employees world wide • Main focus: To develop and sell methacrylate monolithic columns & develop methods and processes for large biomolecules separation and purification. BIA Separations – Products and Services CIM Contract monolithic Research columns Laboratory Method development and Technical Support Important Milestones • 2004: First monolith used for the industrial cGMP purification for plasmid DNA at Boehringer Ingelheim provide 15-fold increase in productivity • 2006: First cGMP production of a vaccine (influenza) using CIM® • 2008: OEM Partnership with Agilent Technologies – develop and produce analytical monolithic columns for PAT • In 2011 BIA Separations was awarded by KAPPA-Health as a model SME in the EU Co-funded research projects • 2012: co-marketing and -
P53 Regulates Biosynthesis Through Direct Inactivation of Glucose-6-Phosphate Dehydrogenase
LETTERS p53 regulates biosynthesis through direct inactivation of glucose-6-phosphate dehydrogenase Peng Jiang1,2,4, Wenjing Du1,2,4, Xingwu Wang1, Anthony Mancuso2, Xiang Gao3, Mian Wu1,5 and Xiaolu Yang2,5 Cancer cells consume large quantities of glucose and primarily link to glycolysis, the regulation of the PPP in tumour cells use glycolysis for ATP production, even in the presence of remains unclear. adequate oxygen1,2. This metabolic signature (aerobic To investigate whether p53 modulates the PPP, we compared the glycolysis or the Warburg effect) enables cancer cells to direct oxidative PPP flux in isogenic p53C=C and p53−=− human colon glucose to biosynthesis, supporting their rapid growth and cancer HCT116 cells11. Cells were cultured in medium containing proliferation3,4. However, both causes of the Warburg effect [2-13C]glucose, and the glucose metabolites were measured by nuclear and its connection to biosynthesis are not well understood. magnetic resonance (NMR) spectroscopy. As shown in Fig. 1a, the Here we show that the tumour suppressor p53, the most absence of p53 resulted in a strong enhancement (∼50%) in oxidative frequently mutated gene in human tumours, inhibits the PPP flux, indicating that p53 suppresses the PPP. The absence of p53 pentose phosphate pathway5 (PPP). Through the PPP, p53 concomitantly led to a strong increase in glucose consumption, and this suppresses glucose consumption, NADPH production and was observed in both HCT116 and mouse embryonic fibroblast (MEF) biosynthesis. The p53 protein binds to glucose-6-phosphate cells (Fig. 1b,c). Inhibition of G6PD using either small interfering RNA dehydrogenase (G6PD), the first and rate-limiting enzyme of (siRNA) or dehydroepiandrosterone (DHEA) reversed the increase in the PPP, and prevents the formation of the active dimer. -
Control of Cell Division: Models from Microorganisms
[CANCER RESEARCH 28, 1802-1809,September 1968] Control of Cell Division: Models from Microorganisms Arthur B. Pardee Program in Biochemical Sciences, Moffett Laboratory, Princeton University, Princeton, New Jersey 08540 Control of Cell Division of a few years ago on the bacterial division cycle are sum One approach to the discovery of a difference between nor marized (12). The reviews furnish a guide to the literature mal and malignant cells is to investigate the regulation of cell before 1966. division. Normal tissues are regulated so that their cells are in a steady-state balance between duplication and destruction. Bacterial Division Malignant cells appear to duplicate unceasingly and are not Most investigations of bacterial division have been carried out with the closely related Gram-negative staining organisms in balance with the rest of the organism; they appear to have lost a control mechanism for cell division. Our problem is to Escherichia coli and Salmonella typhimurium. These organisms are implied unless otherwise stated. Gram-positive Bacillus determine how normal control mechanisms function, how they are deranged in malignant cells, and how they can be restored. species have been used for some fundamental studies on chro The working hypothesis of this article is that the funda mosome replication and for morphologic investigations. It is mental biochemical events which regulate cell division are too early to say whether important differences of cell division similar in both bacteria and higher organisms. This hypothesis regulation exist between different bacteria. Major points of will be useful at present to the extent that bacteria provide bacterial division and chromosomal duplication are illustrated a logical framework for ideas and experiments regarding an schematically in Chart 1. -
Simian Adenovirus Vector Production for Early-Phase Clinical Trials: A
Vaccine 37 (2019) 6951–6961 Contents lists available at ScienceDirect Vaccine journal homepage: www.elsevier.com/locate/vaccine Simian adenovirus vector production for early-phase clinical trials: A simple method applicable to multiple serotypes and using entirely disposable product-contact components Sofiya Fedosyuk a, Thomas Merritt b, Marco Polo Peralta-Alvarez a, Susan J Morris a, Ada Lam c, Nicolas Laroudie d, Anilkumar Kangokar c, Daniel Wright a, George M Warimwe e,f, Phillip Angell-Manning b, ⇑ Adam J Ritchie a, Sarah C Gilbert a, Alex Xenopoulos g, Anissa Boumlic d, Alexander D Douglas a, a Jenner Institute, University of Oxford, Roosevelt Drive, Oxford OX3 7BN, UK b Clinical Biomanufacturing Facility, University of Oxford, Roosevelt Drive, Oxford OX3 7JT, UK c Millipore (UK) Ltd. Bedfont Cross, Stanwell Road, TW14 8NX Feltham, UK d Millipore SAS, 39 Route Industrielle de la Hardt, Molsheim 67120, France e Centre for Tropical Medicine and Global Health, University of Oxford, Roosevelt Drive, Oxford OX3 7FZ, UK f KEMRI-Wellcome Trust Research Programme, P.O. 230-80108 Kilifi, Kenya g EMD Millipore Corporation, 80 Ashby Road, Bedford, MA 01730, USA article info abstract Article history: A variety of Good Manufacturing Practice (GMP) compliant processes have been reported for production Available online 30 April 2019 of non-replicating adenovirus vectors, but important challenges remain. Most clinical development of adenovirus vectors now uses simian adenoviruses or rare human serotypes, whereas reported manufac- Keywords: turing processes mainly use serotypes such as AdHu5 which are of questionable relevance for clinical Simian adenovirus vaccine development. Many clinically relevant vaccine transgenes interfere with adenovirus replication, GMP whereas most reported process development uses selected antigens or even model transgenes such as Clinical trials fluorescent proteins which cause little such interference. -
Restriction Point Control of Cell Growth by a Labile Protein
Proc. NatL Acad. Sci. USA Vol. 79, pp. 436-440, January 1982 Cell Biology Restriction point control of cell growth by a labile protein: Evidence for increased stability in transformed cells (animal cells/transformation/protein degradation/cell cycle/growth control) JUDITH CAMPISI, ESTELA E. MEDRANO*, GAIL MORREO, AND ARTHUR B. PARDEEt Department of Pharmacology, Harvard Medical School, and Division ofCell Growth and Regulation, Sidney Farber Cancer Institute, 44 Binney Street, Boston, Massachusetts 02115 Contributed by Arthur B. Pardee, September 14, 1981 ABSTRACT It has been proposed that animal cells must ac- mouse 3T3 cells at 2-3 hr prior to the onset of DNA synthesis cumulate a labile protein(s) before they can pass the restriction (7, 8). (R) point in the G1 phase ofthe cell cycle [Rossow, P. W., Riddle, What is the biochemical nature of the R point? Two types of V. G. H. & Pardee, A. B. (1979) Proc NatL Acad Sci USA 76, experiments have led to the hypothesis that afunctionally short- 4446-4450]. Here, we present evidence that this R protein ac- lived (labile) regulatory protein(s) (R protein), whose synthesis quires increased stability in transformed 3T3 cells, thereby allow- is sensitive to environmental conditions, need accumulate to a ing these cells to continue growth under conditions that arrest critical amount before a cell can pass the R point and proceed untransformed cells. Low doses of cycloheximide or histidinol towards DNA synthesis. First, pulses ofhigh concentrations of drastically reduced the rate at which normal 3T3 (A31) fibroblasts cycloheximide (CHM), administered to synchronized cultures, in early G, could enter DNA synthesis. -
The Role of Metals in Enzyme Activity*
ANNALS OF CLINICAL AND LABORATORY SCIENCE, Vol. 7, No. 2 Copyright © 1977, Institute for Clinical Science The Role of Metals in Enzyme Activity* JAMES F. RIORDAN, Ph.D. Biophysics Research Laboratory, Department of Biological Chemistry, Harvard Medical School, and Division of Medical Biology, Veter Bent Brigham Hospital, Boston, MA 02115 ABSTRACT Metal ions play important roles in the biological function of many en zymes. The various modes of metal-protein interaction include metal-, ligand-, and enzyme-bridge complexes. Metals can serve as electron donors or acceptors, Lewis acids or structural regulators. Those that participate directly in the catalytic mechanism usually exhibit anomalous physicochemical characteristics reflecting their entatic state. Carboxypep- tidase A, liver alcohol dehydrogenase, aspartate transcarbamoylase and al kaline phosphatase exemplify the different roles of metals in metalloen- zymes while the nucleotide polymerases point to the essential role of zinc in maintaining normal growth and development. Introduction At present, reliable measurements of small concentrations of metals present in Certain metals have long been recog tissues, cells, subcellular particles, body nized to have important biological func fluids and biomacromolecules can be tions primarily as a consequence of nu performed by colorimetry, fluorimetry, tritional investigations.14,15,22 Thus, the polarography, emission spectrometry absence of a specific, essential metal with spark, flame or plasma excitation from the diet of an organism -
Poly(ADP-Ribosyl)Ation of P53 During Apoptosis in Human Osteosarcoma Cells1
[CANCER RESEARCH 59, 2190–2194, May 1, 1999] Poly(ADP-ribosyl)ation of p53 during Apoptosis in Human Osteosarcoma Cells1 Cynthia M. Simbulan-Rosenthal, Dean S. Rosenthal, RuiBai Luo, and Mark E. Smulson2 Department of Biochemistry and Molecular Biology, Georgetown University School of Medicine, Washington, DC 20007 ABSTRACT separation of its DNA binding domain from its catalytic site essentially inactivates the enzyme. PARP has also been implicated in the induction Spontaneous apoptosis in human osteosarcoma cells was observed to be of p53 expression during apoptosis (25) The specific proteolytic cleavage associated with a marked increase in the intracellular abundance of p53. of PARP by caspase-3 is a key apoptotic event because PARP cleavage Immunoprecipitation and immunoblot analysis revealed that, together with a variety of other nuclear proteins, p53 undergoes extensive poly- and inactivation as well as subsequent apoptotic events are blocked by a (ADP-ribosyl)ation early during the apoptotic program in these cells. peptide inhibitor of this protease (23, 26). Subsequent degradation of poly(ADP-ribose) (PAR), attached to p53 pre- We have shown recently that a transient poly(ADP-ribosyl)ation of sumably by PAR glycohydrolase, the only reported enzyme to degrade nuclear proteins in intact human osteosarcoma cells occurs early in PAR, was apparent concomitant with the onset of proteolytic processing apoptosis, prior to commitment to cell death, and is subsequently and activation of caspase-3, caspase-3-mediated cleavage of poly(ADP- followed by cleavage and inactivation of PARP (24). No PAR is ribose) polymerase (PARP), and internucleosomal DNA fragmentation synthesized at the later stages of apoptosis, despite the presence of a during the later stages of cell death. -
University of California, San Diego
UNIVERSITY OF CALIFORNIA, SAN DIEGO Design and Characterization of an Allosteric Metalloprotein Assembly A dissertation submitted in partial satisfaction of the requirements for the degree of Doctor of Philosophy in Chemistry by Lewis Anthony Churchfield Committee in charge: Professor F. Akif Tezcan, Chair Professor Michael D. Burkart Professor Neal K. Devaraj Professor Tracy M. Handel Professor Valerie A. Schmidt 2018 Copyright Lewis Anthony Churchfield, 2018 All rights reserved. Signature Page This Dissertation of Lewis Anthony Churchfield is approved, and it is acceptable in quality and form for publication on microfilm and electronically: Chair University of California, San Diego 2018 iii EPIGRAPH Epigraph Sometimes science is more art than science. Dr. Rick Sanchez iv TABLE OF CONTENTS Table of Contents Signature Page ................................................................................................................... iii Epigraph ............................................................................................................................. iv Table of Contents ................................................................................................................ v List of Abbreviations ........................................................................................................ vii List of Figures .................................................................................................................... ix List of Tables .................................................................................................................. -
Monolithic Columns for Purification and In-Process Control of Viruses and Virus-Like Particles" in "Vaccine Technology IV", B
Engineering Conferences International ECI Digital Archives Vaccine Technology IV Proceedings Spring 5-24-2012 Monolithic Columns for Purification and In- process Control of Viruses and Virus-like Particles Lidija Urbas BIA Separations Milos Barut BIA Separations Follow this and additional works at: http://dc.engconfintl.org/vaccine_iv Part of the Biomedical Engineering and Bioengineering Commons Recommended Citation Lidija Urbas and Milos Barut, "Monolithic Columns for Purification and In-process Control of Viruses and Virus-like Particles" in "Vaccine Technology IV", B. Buckland, University College London, UK; J. Aunins, Janis Biologics, LLC; P. Alves , ITQB/IBET; K. Jansen, Wyeth Vaccine Research Eds, ECI Symposium Series, (2013). http://dc.engconfintl.org/vaccine_iv/43 This Conference Proceeding is brought to you for free and open access by the Proceedings at ECI Digital Archives. It has been accepted for inclusion in Vaccine Technology IV by an authorized administrator of ECI Digital Archives. For more information, please contact [email protected]. Monolithic Columns for Purification and In-process Control of Viruses and Virus-like Particles Lidija Urbas, Miloš Barut Faro, May 24th 2012 Outline • Conventional particle based chromatography • Monolith based chromatography • Downstream processing of Ad3 VLPs – Case study • Convective interaction media (CIM) monoliths for in-process control – CIMac monolithic analytical columns as a tool for HPLC based analytical methods BIA Separations • BIA Separations was founded in September 1998. • Headquartes in Austria, R&D and Production in Slovenia. • BIA Separations USA established in September 2007 - sales and tech support office. • BIA Separations China established in January 2011 - sales and tech support office. • Main focus: To develop and sell methacrylate monolithic columns & develop methods and processes for large biomolecules separation and purification .