Literature DB >> 9353714

Concept and early development of solid-phase peptide synthesis.

B Merrifield1.   

Abstract

There are several reasons for the success of the solid-phase approach to peptide synthesis. The first is the ease of the procedure, the acceleration of the overall process, and the ability to achieve good yields of purified products. The second was the unanticipated discovery of many new biologically active peptides and the expanded need for synthetic peptides to help solve problems in virtually all disciplines of biology. In many cases, the solid-phase technique has been the method of choice. This approach, of course, does not replace the classic solution synthesis methods, but rather supplements them. The choice of techniques depends on the objectives of the synthesis. When carefully worked out, the solution methods can give high yields of highly purified products in large quantities. Many superb syntheses of active peptides have been achieved in this way. The solid-phase method has also yielded many large active peptides. It is particularly useful when large numbers of analogs, in relatively small quantities, are required as in structure-function studies on hormones, growth factors, antibiotics, and other biologically active peptides or for determining the antigenic epitopes of proteins. In addition, it has on occasion been scaled up for production of kilogram quantities. One of the unique uses of solid-phase synthesis has been the synthesis of peptide libraries. Most of the work on this new field in which thousands or millions of peptides are prepared simultaneously has been by solid-phase methods. This new technique is proving to be of great practical importance in rapid drug discovery of peptide, peptide mimetic, and nonpeptide compounds. Developments in screening methods now allow the examination of large numbers of compounds, and active products with structures unpredictable from natural product sequences are being found in this way. The properties of the solid-phase system, the changes in the chemistry, and the applications of the technique to biological problems are discussed in detail in subsequent articles of this volume.

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Year:  1997        PMID: 9353714     DOI: 10.1016/s0076-6879(97)89040-4

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  16 in total

Review 1.  Chemical genetics: ligand-based discovery of gene function.

Authors:  B R Stockwell
Journal:  Nat Rev Genet       Date:  2000-11       Impact factor: 53.242

2.  Stability and specificity of heterodimer formation for the coiled-coil neck regions of the motor proteins Kif3A and Kif3B: the role of unstructured oppositely charged regions.

Authors:  M S Chana; B P Tripet; C T Mant; R Hodges
Journal:  J Pept Res       Date:  2005-02

Review 3.  Structure-function relationships of pre-fibrillar protein assemblies in Alzheimer's disease and related disorders.

Authors:  F Rahimi; A Shanmugam; G Bitan
Journal:  Curr Alzheimer Res       Date:  2008-06       Impact factor: 3.498

4.  Anti-Listeria activities of Galleria mellonella hemolymph proteins.

Authors:  Krishnendu Mukherjee; Mobarak Abu Mraheil; Silke Silva; Daniela Müller; Franz Cemic; Jürgen Hemberger; Torsten Hain; Andreas Vilcinskas; Trinad Chakraborty
Journal:  Appl Environ Microbiol       Date:  2011-04-29       Impact factor: 4.792

5.  Experimental and theoretical study of the mechanism of hydrolysis of substituted phenyl hexanoates catalysed by globin in the presence of surfactant.

Authors:  Selami Ercan; Nevin Arslan; Safak Ozhan Kocakaya; Necmettin Pirinccioglu; Andrew Williams
Journal:  J Mol Model       Date:  2014-02-22       Impact factor: 1.810

6.  Peptide lipidation stabilizes structure to enhance biological function.

Authors:  Brian P Ward; Nickki L Ottaway; Diego Perez-Tilve; Dejian Ma; Vasily M Gelfanov; Matthias H Tschöp; Richard D Dimarchi
Journal:  Mol Metab       Date:  2013-09-05       Impact factor: 7.422

7.  Accelerating the development of novel molecular imaging probes: a role for high-throughput screening.

Authors:  H Charles Manning; Adam Lander; Eliot McKinley; Nathan J Mutic
Journal:  J Nucl Med       Date:  2008-08-14       Impact factor: 10.057

8.  The (1)H NMR structure of bovine Pb(2+)-osteocalcin and implications for lead toxicity.

Authors:  T L Dowd; L Li; C M Gundberg
Journal:  Biochim Biophys Acta       Date:  2008-08-27

Review 9.  Design of functional metalloproteins.

Authors:  Yi Lu; Natasha Yeung; Nathan Sieracki; Nicholas M Marshall
Journal:  Nature       Date:  2009-08-13       Impact factor: 49.962

10.  The three-dimensional structure of bovine calcium ion-bound osteocalcin using 1H NMR spectroscopy.

Authors:  T L Dowd; J F Rosen; L Li; C M Gundberg
Journal:  Biochemistry       Date:  2003-07-01       Impact factor: 3.162

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