Literature DB >> 20180552

Direct solid-phase synthesis of the beta-amyloid (1-42) peptide using controlled microwave heating.

Bernadett Bacsa1, Szilvia Bosze, C Oliver Kappe.   

Abstract

Standard linear Fmoc/t-Bu solid-phase synthesis of the 42-mer beta-amyloid (1-42) peptide was achieved under controlled microwave conditions at 86 degrees C using inexpensive DIC/HOBt as coupling reagent on ChemMatrix resin. In order to avoid racemization of the sensitive amino acids, the coupling of the three His residues in the difficult peptide sequence was performed at room temperature. The desired peptide was obtained within 15 h overall processing time in high yield and purity (78% crude yield).

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Year:  2010        PMID: 20180552     DOI: 10.1021/jo100136r

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  12 in total

1.  Improved chemical synthesis of hydrophobic Aβ peptides using addition of C-terminal lysines later removed by carboxypeptidase B.

Authors:  Saketh Chemuru; Ravindra Kodali; Ronald Wetzel
Journal:  Biopolymers       Date:  2014-03       Impact factor: 2.505

2.  Efficient microwave-assisted synthesis of human islet amyloid polypeptide designed to facilitate the specific incorporation of labeled amino acids.

Authors:  Peter Marek; Ann Marie Woys; Kelvin Sutton; Martin T Zanni; Daniel P Raleigh
Journal:  Org Lett       Date:  2010-11-05       Impact factor: 6.005

3.  N-Amino peptide scanning reveals inhibitors of Aβ42 aggregation.

Authors:  Khalilia C Tillett; Juan R Del Valle
Journal:  RSC Adv       Date:  2020-04-08       Impact factor: 3.361

Review 4.  Advances in Fmoc solid-phase peptide synthesis.

Authors:  Raymond Behrendt; Peter White; John Offer
Journal:  J Pept Sci       Date:  2016-01       Impact factor: 1.905

5.  Decreasing amyloid toxicity through an increased rate of aggregation.

Authors:  Silvia Sonzini; Helen F Stanyon; Oren A Scherman
Journal:  Phys Chem Chem Phys       Date:  2017-01-04       Impact factor: 3.676

6.  Epimerization-free access to C-terminal cysteine peptide acids, carboxamides, secondary amides, and esters via complimentary strategies.

Authors:  Christine A Arbour; Thilini D Kondasinghe; Hasina Y Saraha; Teanna L Vorlicek; Jennifer L Stockdill
Journal:  Chem Sci       Date:  2017-11-09       Impact factor: 9.825

7.  An Optimised Di-Boronate-ChemMatrix Affinity Chromatography to Trap Deoxyfructosylated Peptides as Biomarkers of Glycation.

Authors:  Monika Kijewska; Francesca Nuti; Magdalena Wierzbicka; Mateusz Waliczek; Patrycja Ledwoń; Agnieszka Staśkiewicz; Feliciana Real-Fernandez; Giuseppina Sabatino; Paolo Rovero; Piotr Stefanowicz; Zbigniew Szewczuk; Anna Maria Papini
Journal:  Molecules       Date:  2020-02-10       Impact factor: 4.411

8.  Semi-synthesis and analysis of chemically modified zif268 zinc-finger domains.

Authors:  Friederike Fehr; André Nadler; Florian Brodhun; Ivo Feussner; Ulf Diederichsen
Journal:  ChemistryOpen       Date:  2012-01-02       Impact factor: 2.911

9.  An explorative study towards the chemical synthesis of the immunoglobulin G1 Fc CH3 domain.

Authors:  Luigi Grassi; Cornelia Roschger; Vesna Stanojlović; Chiara Cabrele
Journal:  J Pept Sci       Date:  2018-10-22       Impact factor: 1.905

Review 10.  Challenges and Perspectives in Chemical Synthesis of Highly Hydrophobic Peptides.

Authors:  Lena K Mueller; Andreas C Baumruck; Hanna Zhdanova; Alesia A Tietze
Journal:  Front Bioeng Biotechnol       Date:  2020-03-04
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