The solid-phase method introduced by Merrifield is now firmly established as a powerful technique for the study of biologically important peptides. Synthesis normally begins by covalently liking the C-terminal amino acid residue of the desired peptide to an insoluble polymeric support. This anchoring step is an integral part of the overall synthetic plan, and the experimental details can impact significantly on the overall purity and yield of the final product. As part of our general interest in achieving milder chemical methods for peptide synthesis, we have had several occasions to pursue the advantages of """"""""handle"""""""" approaches to anchoring. Handles are defined as bifunctional spacers which serve to attach the initial residue to the polymeric support in two discrete steps. They allow precise control over the stability and ultimate cleavage of the anchoring linkage, and facilitate quantitative attachments which circumvent problems associated with extraneous polymer-bound functional groups. Handles developed in our laboratory are compatible with readily removable N alpha-amino protecting groups such as the highly acid-labile N alpha-biphenylyl- isopropyloxycarbonyl (Bpoc), the base-labile N alpha-9-fluorenylmethyloxycarbonyl (Fmoc), and the thiolysable N alpha-dithiasuccinoyl (Dts) or N alpha-3-nitro-2-pyridine-sulfenyl (Npys) functions. Cleavages of the anchoring linkages occur under relatively mild conditions with acid, light, or fluoride ion; the products may be peptide acids or amides. Application of these handles in orthogonal protection schemes offers the further possibility of preparing partially protected segment suitable for purification followed by restitching to make longer and more complicated products. The present proposal aims to take several handles that have already been worked out in simple systems and demonstrate their scope when applied to challenging peptide targets. Simultaneously, some modified and new chemistries are suggested that may lead to new handles with even better properties and/or a wider range of applications.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM042722-02
Application #
3301548
Study Section
Bio-Organic and Natural Products Chemistry Study Section (BNP)
Project Start
1989-07-01
Project End
1993-06-30
Budget Start
1990-07-01
Budget End
1991-06-30
Support Year
2
Fiscal Year
1990
Total Cost
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Type
Other Domestic Higher Education
DUNS #
168559177
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Barany, George; Britton, Doyle; Chen, Lin et al. (2015) Unexpectedly Stable (Chlorocarbonyl)(N-ethoxycarbonylcarbamoyl)disulfane, and Related Compounds That Model the Zumach-Weiss-Kühle (ZWK) Reaction for Synthesis of 1,2,4-Dithiazolidine-3,5-diones. J Org Chem 80:11313-21
Barany, Michael J; Hammer, Robert P; Merrifield, R B et al. (2005) Efficient synthesis of 1,2,4-dithiazolidine-3,5-diones [dithiasuccinoyl-amines] from bis(chlorocarbonyl)disulfane plus bis(trimethylsilyl)amines. J Am Chem Soc 127:508-9
Kappel, Joseph C; Barany, George (2005) A convenient orthogonally cleavable methionine handle for anchoring amines to polymeric supports. J Comb Chem 7:78-84
Kappel, Joseph C; Barany, George (2005) Backbone amide linker (BAL) strategy for Nalpha-9-fluorenylmethoxycarbonyl (Fmoc) solid-phase synthesis of peptide aldehydes. J Pept Sci 11:525-35
Cironi, Pablo; Tulla-Puche, Judit; Barany, George et al. (2004) Solid-phase syntheses of furopyridine and furoquinoline systems. Org Lett 6:1405-8
Tulla-Puche, Judit; Barany, George (2004) On-resin native chemical ligation for cyclic peptide synthesis. J Org Chem 69:4101-7
Shannon, Simon K; Barany, George (2004) Colorimetric monitoring of solid-phase aldehydes using 2,4-dinitrophenylhydrazine. J Comb Chem 6:165-70
Shannon, Simon K; Barany, George (2004) 4-(9-fluorenylmethyloxycarbonyl)phenylhydrazine (FmPH): a new chromophoric reagent for quantitative monitoring of solid-phase aldehydes(1-3). J Org Chem 69:4586-94
Shannon, Simon K; Peacock, Mandy J; Kates, Steven A et al. (2003) Solid-phase synthesis of lidocaine and procainamide analogues using backbone amide linker (BAL) anchoring. J Comb Chem 5:860-8
Barany, George; Han, Yongxin; Hargittai, Balazs et al. (2003) Side-chain anchoring strategy for solid-phase synthesis of peptide acids with C-terminal cysteine. Biopolymers 71:652-66

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