Tag: MultiPep

10. März 2021, ab 10.15 Uhr

Erleben Sie einen ganzen Tag interessante Vorträge zu den Neuigkeiten der Peptid-Synthese. Aufgrund der Corona-Situation können Präsenzvorträge derzeit nicht stattfinden. Deshalb veranstaltet CEM zusammen mit bekannten Forschern/innen dieses kostenfreie Online Seminar.

Academic Guest Speakers:


Professor Anna Maria Papini

University of Florence,

CY Cergy Paris Université

The challenge to design fully automated solid-phase MW-assisted cGMP ready processes of peptide production as active pharmaceutical ingredients 

Interdepartmental Research Unit of Peptide & Protein Chemistry and Biology, Departments  of Chemistry and NeuroFarBa, University of Florence (Italy)

With the increase of approved peptide-based drugs and patents expiring, the manufacturers’ need in production of peptides is dramatically rising. Companies involved in peptide-based drugs that have to be compliant with good manufacturing practices (GMP), face several challenges, such as high production costs on downstream processes (due to the use of high raw material amounts) and bad scalability. Therefore, the main challenge of production of active peptides as pharmaceutical ingredients is to find solutions to specific problems encountered during scale-up. 

As a proof-of concept we will report the strategies we investigated for the preparation of Eptifibatide, scalable to kilogram-scale, having in common the use of the microwave-assisted solid-phase peptide synthesis (MW-SPPS) procedure, which is now available not only at R&D level but also for the large-scale manufacturing of peptides. Following the very fast microwave-assisted Fmoc/tBu synthesis of the Eptifibatide linear precursor by a DIC/Oxyma Pure coupling protocol at 90 °C, we explored both the solution (off-resin) and the solid-phase (on-resin) disulfide bond formation.

The relevance of the strategy we optimized is essentially based on the selection of the StBu orthogonal protection on cysteine that is easily removed by MPA acting as a novel reducing agent for Cys(StBu) deprotection. Moreover, we demonstrated that all operations can be performed by fully automated process in the instrumentation.

To the best of our knowledge, this is a unique strategy performing all the processes including disulfide bond formation in a single reactor and represents an optimized scalable fully automated solid-phase microwave-assisted cGMP-ready process to prepare Eptifibatide.


Designing Synthetic Peptides to Explore the Dark Matter of Protein Space

Dek Woolfson

Schools of Chemistry and Biochemistry, & Bristol BioDesign Institute

University of Bristol, UK

Protein design—i.e., the construction of entirely new protein sequences that fold into prescribed structures—has come of age: it is now possible to generate a wide variety stable protein folds from scratch using rational and/or computational approaches.  A new challenge for the field is to move past protein structures offered up by nature and to target the so-called ‘dark matter of protein space’; that is, protein structures that should be possible in terms of chemistry and physics, but which biology seems to have overlook or not used prolifically.  This talk will illustrate what is currently possible in this nascent field using de novo a-helical coiled-coil peptides as building blocks for assembling larger, more-complex and functional protein-like structures.1

Coiled coils are bundles of 2 or more a helices that wrap around each other to form rope-like structures.  They are one of the dominant structures that direct natural protein-protein interactions. Our understanding of coiled coils provides a strong basis for building new proteins from first principles.  The first part of my talk will survey this understanding,1 our design methods,2,3 and our current “toolkit” of de novo coiled coils.4-5

Next, I will describe how the toolkit can be expanded used to generate some dark-matter protein structures.  I’ll focus on the rational and computational design of a-helical barrel proteins, which have 5 or more helices surrounding accessible central channels.6  Finally, I’ll discuss how these synthetic barrel proteins can be put to use to make new nanotube materials,7 rudimentary catalysts,8 membrane-spanning pores,9 and the components of a new types of sensing devices.10

Professor Dek Woolfson

University of Bristol


Professor Fernando Albericio

University of Barcelona,

University of Kwazulu-Natal

Microwave-Assisted Solid-Phase Peptide Synthesis, A Unique Tool for Peptide Research

Fernando Albericio,1,2 Beatriz G. de la Torre1

1University of KwaZulu-Natal, Durban 4001, South Africa; 2University of Barcelona, 08028-Barcelona, Spain

During the last five years (2016-2020), 18 drugs containing peptides have been approved by the US FDA.  In addition, several hundred are in clinical phases or advanced preclinical studies.   The development of new synthetic strategies has facilitated this explosion in the world of peptides. In this regard, the development of new resins, coupling reagents, protecting groups, and, more importantly, reliable and robust peptide synthesizers have been vital for the consolidation of the peptide drug market. 

In the field of automatic synthesizers, the last breakthrough occurred when at the beginning of this century, CEM launched the new concept of Microwave-Assisted SPPS. Our group and others have demonstrated that both couplings and Fmoc-removal are better performed in the microwave mode compared with classical synthesis or even with conventional heating. More important, this better performance in the two key reactions is not accompanied by any significant side-reaction. 

This presentation will discuss our last results on the use of Microwave synthesis for the preparation of intriguing peptides and/or for developing new synthetic strategies: (i) the preparation of staple peptides via late-stage C(sp2)-H Pd activation using the microwave; (ii) synthesis of N-alkyl amino acid containing peptides; (iii) development of new and more efficient coupling reagents; and (iv) microwave-based Green Solid-Phase Peptide Synthesis (GSPPS). 

 

In the GSPPS, the CEM Liberty Blue Microwave technology by itself could be considered green in terms of solvent consumption and time-saving and due to the excellent quality of the crude peptides, which enormously facilitates the purification with the consequent increase of yield and reduction of chromatography solvents.


Short antimicrobial peptides – discovery and optimization 

Kai Hilpert, St George’s University

The global health threat surrounding bacterial resistance has resulted in antibiotic researchers shifting their focus away from ‘traditional’ antibiotics and concentrating on other antimicrobial agents, including antimicrobial peptides.

These peptides exhibit broad-spectrum activity against bacteria, including multi-drug resistant strains, viruses, fungi, and protozoa, and constitute a major element of the innate immune system of many multicellular organisms.

We use the Spot-synthesis technique to study and optimize naturally occurring as well as artificial antimicrobial peptides. Understanding the features that make them antibacterial and hemolytic allows for targeted drug development. 

Associate Professor Kai Hilpert

St George’s University

 

Der Zeitliche Ablauf

 

Registrieren Sie sich hier kostenfrei

Capturing the interaction between histones and their deacetylases with hydroxamic acid-modified microarrays

Histone deacetylases (HDACs) modify the epigenetic code recorded on histones. This landscape of modifications can be altered with drugs, such as HDAC inhibitors, to silence genes involved in cancer progression. Studying the HDAC‒histone interaction may help elucidate these mechanisms.

Artikel lesen

 

Die steigende Nachfrage nach synthetischen Peptiden, die zu den wichtigsten Biomolekülen in der Forschung gehören, erfordert äußerst effiziente automatisierte Synthesizer. Synthetische Peptide sind wesentliche Werkzeuge für eine Vielzahl biochemischer Experimente. Peptide fungieren beispielsweise als Hormone, Neurotransmitter oder als Signalmoleküle in der Immunantwort.

Peptide teilen die Überlegenheit von Proteinen, sind jedoch signifikant kleiner und daher mit chemischen Strategien kostengünstig zu synthetisieren. Dadurch bieten sie eine umfassende Perspektive für ein neuartiges Wirkstoffdesign. Die hohe Wirksamkeit, Selektivität und Spezifität von Peptiden zu ihren jeweiligen biologischen Zielstrukturen haben in den letzten Jahren zu enormen Fortschritten bei therapeutischen Anwendungen geführt und sind für die Arzneimittelentwicklung von großem Vorteil.

Die automatisierte Lösung

Neue Fragestellungen der Proteomforschung, die zur Identifizierung von Zielpeptiden oder -proteinen geführt haben, können oft nur durch den Vergleich mit einer großen Anzahl verschiedener Peptide beantwortet werden. Diese werden in Milligramm-Mengen benötigt und können mit den automatisierten parallelen Synthesizern MultiPep 1 oder MultiPep 2 synthetisiert werden. Die automatisierte Festphasenpeptidsynthese (SPPS) bietet dafür eine geeignete Technologie zur Herstellung synthetischer Peptide. CEM hat die bewährten MultiPep Peptidsynthesizer von Intavis übernommen und entwickelt sie weiter als Ergänzung zu den Liberty Mikrowellen-Peptid-Synthesizern.

Artikel lesen

Im kostenfreien Web-Seminar erläutern die Referenten Frau Dr. Monika Swiontek und Herr Dr. Christian Behn die unterschiedlichen Techniken zur schnellen und flexiblen Peptid-Synthese.

Die Synthese unter Mikrowellenaktivierung ermöglicht in wenigen Stunden die Darstellung reiner Peptide statt wie üblich in vielen Tagen. Synthesemaßstäbe von Milligramm Mengen bis zur Produktion im kg-Bereich werden vorgestellt. Während einer live Vorführung im Labor erleben Sie einen Kopplungszyklus und lernen dabei die einfache intuitive Software kennen. In Ergänzung dazu werden flexible Formate der multiplen parallelen Synthese vorgestellt, wie z. B. SPOT-Synthese, Festphasensynthese in 96er Filterplatten- und Filtersäulen zur Synthese von Peptid- und PNA-Bibliotheken. Zusätzlich wird ein Aspekt der beiden Referenten auf die Abspaltung der fertig synthetisierten Peptide gelegt und es werden zwei moderne Cleavage-Systeme vorgestellt.

Mittwoch, den 9. Dezember 2020, 10.00 – 11.30 Uhr und 14.00 – 15.30 Uhr

Hier kostenfrei anmelden

0

CEM und Intavis gehen gemeinsam neue Wege

Seit dem 01.03.2020 hat die Firma CEM die Produkte der Firma Intavis in ihr Produktportfolio übernommen.

Um unseren neuen Kunden die Zusammenarbeit weiter einfach zu machen, werden die Produkte beider Firmen unverändert weitergeführt. Auch die Wartung der Geräte bzw. die Reparatur der Geräte wird wie gewohnt stattfinden. Die Verbrauchsmaterialien und Ersatzteile sind nach wie vor erhältlich. Selbst die Ansprechpartner bleiben für unsere Kunden dieselben, nur unter neuen Telefonnummern oder E-Mailadressen.

Was sich für Sie ändert? Es steht Ihnen ein größeres Team an Produktspezialisten, Vertrieb und Service zur Verfügung.