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Relevant bibliographies by topics / Solid-Phase Peptide Synthesis; Spot Synthesis / Journal articles

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Journal articles on the topic 'Solid-Phase Peptide Synthesis; Spot Synthesis'

Author: Grafiati

Published: 4 June 2021

Last updated: 7 February 2022

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1

Li, Wenyi, John D. Wade, Eric Reynolds, and Neil M. O'Brien-Simpson. "Chemical Modification of Cellulose Membranes for SPOT Synthesis." Australian Journal of Chemistry 73, no. 3 (2020): 78. http://dx.doi.org/10.1071/ch19335.

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Since the development of solid-phase peptide synthesis in the 1960s, many laboratories have modified the technology for the production of peptide arrays to facilitate the discovery of novel peptide mimetics and therapeutics. One of these, known as SPOT synthesis, enables parallel peptide synthesis on cellulose paper sheets and has several advantages over other peptide arrays methods. Today, the SPOT technique remains one of the most frequently used methods for synthesis and screening of peptides on arrays. Although polypropylene and glass can be used for the preparation of peptide arrays, the

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2

De-Simone, Salvatore Giovanni, Larissa Rodrigues Gomes, Paloma Napoleão-Pêgo, Guilherme Curty Lechuga, Jorge Soares de Pina, and Flavio Rocha da Silva. "Epitope Mapping of the Diphtheria Toxin and Development of an ELISA-Specific Diagnostic Assay." Vaccines 9, no. 4 (2021): 313. http://dx.doi.org/10.3390/vaccines9040313.

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Background: The diphtheria toxoid antigen is a major component in pediatric and booster combination vaccines and is known to raise a protective humoral immune response upon vaccination. Although antibodies are considered critical for diphtheria protection, little is known about the antigenic determinants that maintain humoral immunity. Methods: One-hundred and twelve 15 mer peptides covering the entire sequence of diphtheria toxin (DTx) protein were prepared by SPOT synthesis. The immunoreactivity of membrane-bound peptides with sera from mice immunized with a triple DTP vaccine allowed mappin

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3

Swiontek, Wasko, Fraczyk, Galecki, Kaminski, and Kolesinska. "Insulin Hot-Spot Analogs Formed with N-Methylated Amino Acid Residues Inhibit Aggregation of Native Hormone." Molecules 24, no. 20 (2019): 3706. http://dx.doi.org/10.3390/molecules24203706.

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In this study, N-methylated analogs of hot-spots of insulin were designed and synthesized, in the expectation that they would inhibit the aggregation of both insulin hot-spots and the entire hormone. Synthesis of insulin “amyloidogenic” analogs containing N-methylated amino acid residues was performed by microwave-assisted solid phase according to the Fmoc/tert-Bu strategy. As a coupling reagent 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium toluene-4-sulfonate (DMT/NMM/TosO-) was used. Three independent methods were applied in aggregation studies of the complexes of insulin with it

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4

Lloyd-Williams, Paul, Fernando Albericio, and Ernest Giralt. "Convergent solid-phase peptide synthesis." Tetrahedron 49, no. 48 (1993): 11065–133. http://dx.doi.org/10.1016/s0040-4020(01)81800-7.

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5

LLOYD-WILLIAMS, PAUL, FERNANDO ALBERICIO, and ERNEST GIRALT. "Convergent solid-phase peptide synthesis." International Journal of Peptide and Protein Research 37, no. 1 (2009): 58–60. http://dx.doi.org/10.1111/j.1399-3011.1991.tb00733.x.

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6

KISO, YOSHIAKI, YOICHI FUJIWARA, TOORU KIMURA, AKIKO NISHITANI, and KENICHI AKAJI. "Efficient solid phase peptide synthesis." International Journal of Peptide and Protein Research 40, no. 3-4 (2009): 308–14. http://dx.doi.org/10.1111/j.1399-3011.1992.tb00306.x.

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7

Grandas, A., E. Pedroso, E. Giralt, C. Granier, and J. Van Rietschoten. "Convergent solid phase peptide synthesis IV." Tetrahedron 42, no. 24 (1986): 6703–11. http://dx.doi.org/10.1016/s0040-4020(01)82111-6.

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8

Le´ger, Roger, Rose Yen, Miles W. She, Ving J. Lee, and Scott J. Hecker. "N-Linked solid phase peptide synthesis." Tetrahedron Letters 39, no. 24 (1998): 4171–74. http://dx.doi.org/10.1016/s0040-4039(98)00777-1.

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9

Felix, Arthur M. "SOLID-PHASE PEPTIDE SYNTHESIS. Bruce Merrifield." Kobunshi 51, no. 8 (2002): 630–32. http://dx.doi.org/10.1295/kobunshi.51.630.

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10

Krchňák, Viktor, Josef Vágner, Martin Flegel, and Otakar Mach. "Continuous-flow solid-phase peptide synthesis." Tetrahedron Letters 28, no. 38 (1987): 4469–72. http://dx.doi.org/10.1016/s0040-4039(00)96541-9.

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11

Giralt, Ernest, Ramon Eritja, Enrique Pedroso, Claude Granier, and Jurphaas Van Rietschoten. "Convergent solid phase peptide synthesis-III." Tetrahedron 42, no. 2 (1986): 691–98. http://dx.doi.org/10.1016/s0040-4020(01)87472-x.

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12

Ramage, R., J. Green, and O. M. Ogunjobi. "Solid phase peptide synthesis of ubiquitin." Tetrahedron Letters 30, no. 16 (1989): 2149–52. http://dx.doi.org/10.1016/s0040-4039(01)93735-9.

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13

O'Donnell, Martin J., Changyou Zhou, and William L. Scott. "Solid-Phase Unnatural Peptide Synthesis (UPS)." Journal of the American Chemical Society 118, no. 25 (1996): 6070–71. http://dx.doi.org/10.1021/ja9601245.

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14

MERRIFIELD, B. "ChemInform Abstract: Solid-Phase Peptide Synthesis." ChemInform 27, no. 29 (2010): no. http://dx.doi.org/10.1002/chin.199629275.

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15

WALKER, B. "ChemInform Abstract: Solid-Phase Peptide Synthesis." ChemInform 27, no. 29 (2010): no. http://dx.doi.org/10.1002/chin.199629279.

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16

DAVIES, J. S. "ChemInform Abstract: Solid Phase Peptide Synthesis." ChemInform 26, no. 32 (2010): no. http://dx.doi.org/10.1002/chin.199532286.

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17

Fields, Gregg B. "ChemInform Abstract: Solid-Phase Peptide Synthesis." ChemInform 30, no. 13 (2010): no. http://dx.doi.org/10.1002/chin.199913316.

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18

Ferderigos, Nikolas, and Christos Zikos. "ChemInform Abstract: Solid-Phase Peptide Synthesis." ChemInform 43, no. 39 (2012): no. http://dx.doi.org/10.1002/chin.201239267.

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19

HANSEN, PAUL ROBERT, ARNE HOLM, and GUNNAR HOUEN. "Solid-phase peptide synthesis on proteins." International Journal of Peptide and Protein Research 41, no. 3 (2009): 237–45. http://dx.doi.org/10.1111/j.1399-3011.1993.tb00331.x.

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20

Ghassemian, Artin, Xavier Vila-Farrés, Paul F. Alewood, and Thomas Durek. "Solid phase synthesis of peptide-selenoesters." Bioorganic & Medicinal Chemistry 21, no. 12 (2013): 3473–78. http://dx.doi.org/10.1016/j.bmc.2013.03.076.

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21

Stewart, John M. "Bradykinin in Solid-phase Peptide Synthesis." International Journal of Peptide Research and Therapeutics 13, no. 1-2 (2006): 3–5. http://dx.doi.org/10.1007/s10989-006-9043-2.

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22

Ottesen, Jennifer J., Maya Bar-Dagan, Baldissera Giovani, and Tom W. Muir. "An amalgamation of solid phase peptide synthesis and ribosomal peptide synthesis." Biopolymers 90, no. 3 (2007): 406–14. http://dx.doi.org/10.1002/bip.20810.

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23

SPATOLA, ARNO F., MOHMED K. ANWER, and MEENA N. RAO. "Phase transfer catalysis in solid phase peptide synthesis." International Journal of Peptide and Protein Research 40, no. 3-4 (2009): 322–32. http://dx.doi.org/10.1111/j.1399-3011.1992.tb00308.x.

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24

Liu, Dan, Ya-Li Guo, Jin Qu, and Chi Zhang. "Recyclable hypervalent-iodine-mediated solid-phase peptide synthesis and cyclic peptide synthesis." Beilstein Journal of Organic Chemistry 14 (May 22, 2018): 1112–19. http://dx.doi.org/10.3762/bjoc.14.97.

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The system of the hypervalent iodine(III) reagent FPID and (4-MeOC6H4)3P was successfully applied to solid-phase peptide synthesis and cyclic peptide synthesis. Four peptides with biological activities were synthesized through SPPS and the bioactive cyclic heptapeptide pseudostellarin D was obtained via solution-phase peptide synthesis. It is worth noting that FPID can be readily regenerated after the peptide coupling reaction.

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25

Sabatino, Giuseppina, Mario Chelli, Alberto Brandi, and Anna Papini. "Analytical Methods for Solid Phase Peptide Synthesis." Current Organic Chemistry 8, no. 4 (2004): 291–301. http://dx.doi.org/10.2174/1385272043485954.

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26

Shin, Dong-Sik, Do-Hyun Kim, Woo-Jae Chung, and Yoon-Sik Lee. "Combinatorial Solid Phase Peptide Synthesis and Bioassays." BMB Reports 38, no. 5 (2005): 517–25. http://dx.doi.org/10.5483/bmbrep.2005.38.5.517.

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27

Burdick, Daniel J., Martin E. Struble, and John P. Burnier. "Solid phase synthesis of peptide para -nitroanilides." Tetrahedron Letters 34, no. 16 (1993): 2589–92. http://dx.doi.org/10.1016/s0040-4039(00)77632-5.

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28

Peters, S., T. Bielfeldt, M. Meldal, K. Bock, and H. Paulsen. "Solid phase peptide synthesis of mucin glycopeptides." Tetrahedron Letters 33, no. 43 (1992): 6445–48. http://dx.doi.org/10.1016/s0040-4039(00)79011-3.

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29

Moss, Jason A., Tobin J. Dickerson, and Kim D. Janda. "Solid phase peptide synthesis on JandaJelTM resin." Tetrahedron Letters 43, no. 1 (2002): 37–40. http://dx.doi.org/10.1016/s0040-4039(01)02076-7.

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30

Jad, Yahya E., Ashish Kumar, Ayman El-Faham, Beatriz G. de la Torre, and Fernando Albericio. "Green Transformation of Solid-Phase Peptide Synthesis." ACS Sustainable Chemistry & Engineering 7, no. 4 (2019): 3671–83. http://dx.doi.org/10.1021/acssuschemeng.8b06520.

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31

Chen, Jack J., and Arno F. Spatola. "Solid phase synthesis of peptide hydroxamic acids." Tetrahedron Letters 38, no. 9 (1997): 1511–14. http://dx.doi.org/10.1016/s0040-4039(97)00143-3.

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32

Fields, Gregg B., and Cynthia g. Fields. "Solvation effects in solid-phase peptide synthesis." Journal of the American Chemical Society 113, no. 11 (1991): 4202–7. http://dx.doi.org/10.1021/ja00011a023.

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33

Tong, Xiao-He, and Anita Hong. "Solid phase synthesis of aspartyl peptide aldehydes." Tetrahedron Letters 41, no. 46 (2000): 8857–60. http://dx.doi.org/10.1016/s0040-4039(00)01615-4.

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34

Pedersen, Søren L., A. Pernille Tofteng, Leila Malik, and Knud J. Jensen. "Microwave heating in solid-phase peptide synthesis." Chem. Soc. Rev. 41, no. 5 (2012): 1826–44. http://dx.doi.org/10.1039/c1cs15214a.

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35

Ulijn, Rein V., Nicola Bisek, Peter J. Halling, and Sabine L. Flitsch. "Understanding protease catalysed solid phase peptide synthesis." Organic & Biomolecular Chemistry 1, no. 8 (2003): 1277–81. http://dx.doi.org/10.1039/b211890d.

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36

KORNREICH, WAYNE, HARRY ANDERSON, JOHN PORTER, WYLIE VALE, and JEAN RIVIER. "Peptide N-alkylamides by solid phase synthesis*." International Journal of Peptide and Protein Research 25, no. 4 (2009): 414–20. http://dx.doi.org/10.1111/j.1399-3011.1985.tb02194.x.

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37

McFERRAN, N. V., B. WALKER, C. D. McGURK, and F. C. SCOTT. "Conductance measurements in solid phase peptide synthesis." International Journal of Peptide and Protein Research 37, no. 5 (2009): 382–87. http://dx.doi.org/10.1111/j.1399-3011.1991.tb00752.x.

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38

ENGLEBRETSEN, DARREN R., and DAVID R. K. HARDING. "Solid phase peptide synthesis on hydrophilic supports." International Journal of Peptide and Protein Research 40, no. 6 (2009): 487–96. http://dx.doi.org/10.1111/j.1399-3011.1992.tb00432.x.

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39

Reczek, Joseph J., Elisa Rebolini, and Adam R. Urbach. "Solid-Phase Synthesis of Peptide−Viologen Conjugates." Journal of Organic Chemistry 75, no. 6 (2010): 2111–14. http://dx.doi.org/10.1021/jo100018f.

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40

Al Musaimi, Othman, Beatriz G. de la Torre, and Fernando Albericio. "Greening Fmoc/tBu solid-phase peptide synthesis." Green Chemistry 22, no. 4 (2020): 996–1018. http://dx.doi.org/10.1039/c9gc03982a.

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41

LLOYD-WILLIAMS, P., F. ALBERICIO, and E. GIRALT. "ChemInform Abstract: Convergent Solid-Phase Peptide Synthesis." ChemInform 25, no. 11 (2010): no. http://dx.doi.org/10.1002/chin.199411324.

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42

ALBERICIO, F., P. LLOYD-WILLIAMS, M. GAIRI, et al. "ChemInform Abstract: Convergent Solid Phase Peptide Synthesis." ChemInform 24, no. 27 (2010): no. http://dx.doi.org/10.1002/chin.199327317.

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43

ALBERICIO, F., P. LLOYD-WILLIAMS, and E. GIRALT. "ChemInform Abstract: Convergent Solid-Phase Peptide Synthesis." ChemInform 29, no. 10 (2010): no. http://dx.doi.org/10.1002/chin.199810312.

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44

Zaoral, Milan. "DDAVP (Desmopressin) and solid phase peptide synthesis." Biopolymers 90, no. 3 (2008): 213. http://dx.doi.org/10.1002/bip.20936.

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45

Behrendt, Raymond, Peter White, and John Offer. "Advances in Fmoc solid‐phase peptide synthesis." Journal of Peptide Science 22, no. 1 (2016): 4–27. http://dx.doi.org/10.1002/psc.2836.

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46

Christensen, Leif, Richard Fitzpatrick, Brian Gildea, et al. "Solid-Phase synthesis of peptide nucleic acids." Journal of Peptide Science 1, no. 3 (1995): 175–83. http://dx.doi.org/10.1002/psc.310010304.

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47

KASPARI, ANNE, ANGELIKA SCHIERHORN, and MIKE SCHUTKOWSKI. "Solid-phase synthesis of peptide-4-nitroanilides." International Journal of Peptide and Protein Research 48, no. 5 (2009): 486–94. http://dx.doi.org/10.1111/j.1399-3011.1996.tb00867.x.

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48

Gogoll, Adolf, and Máté Erdélyi. "Rapid Microwave-Assisted Solid Phase Peptide Synthesis." Synthesis, no. 11 (2002): 1592–96. http://dx.doi.org/10.1055/s-2002-33348.

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49

Bodanszky, Miklos, and Maria A. Bednarek. "Active esters in solid-phase peptide synthesis." Journal of Protein Chemistry 8, no. 4 (1989): 461–69. http://dx.doi.org/10.1007/bf01026430.

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50

Elmore, D. T. "Solid-phase peptide synthesis: a practical approach." FEBS Letters 265, no. 1-2 (1990): 152. http://dx.doi.org/10.1016/0014-5793(90)80916-7.

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