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1.
Methods Mol Biol ; 2178: 217-243, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-33128753

RESUMEN

In this chapter, a protocol to design affinity chromatography matrices with short peptide ligands immobilized for protein purification is described. The first step consists of the synthesis of a combinatorial peptide library on the hydroxymethylbenzoyl (HMBA)-ChemMatrix resin by the divide-couple-recombine (DCR) method using the Fmoc chemistry. Next, the library is screened with the protein of interest labeled with a fluorescent dye or biotin. Subsequently, peptides contained on positive beads are identified by tandem matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS/MS), and those sequences showing greater consensus are synthesized in larger quantities and immobilized on chromatographic supports. Finally, target protein adsorption on peptide affinity matrices is evaluated through equilibrium adsorption isotherms and breakthrough curves.


Asunto(s)
Cromatografía de Afinidad , Técnicas Químicas Combinatorias , Biblioteca de Péptidos , Espectrometría de Masa por Láser de Matriz Asistida de Ionización Desorción
2.
J Genet ; 97(5): 1205-1212, 2018 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-30555070

RESUMEN

Amphibian secretion is an important source of bioactive molecules that naturally protect the skin against noxious microorganisms. Collectively called antimicrobial peptides (AMPs), these molecules have a wide spectrum of action, targeting viruses, bacteria and fungi. Like many membrane and secreted proteins, AMPs have cleavable signal sequences that mediate and translocate the nascent polypeptide chains into the endoplasmic reticulum. Although it is accepted that the signal peptides (SPs) are simple and interchangeable, there is neither sequence nor structure that is conserved among all gene families. They derived from a common ancestor but developed different traits as they adapt to distinct environmental pressures. The aim of this study was to provide anoverview of the diversity of SPs of the frog, taking into account reported cDNA sequences and the evolutionary relationship among them. We analysed more than 2000 records that reported the relative abundance, diversity and evolutionary divergence based on the peptide signals of frog AMPs. We conclude that the physical properties of the sequence are more important than the specific peptidesin AMP SPs. Since there is significant overlapping among related genera, differences in secretion from different peptide types should be regulated by additional levels, such as posttranscriptional modifications or 5-UTR sequences.


Asunto(s)
Proteínas Anfibias/genética , Anfibios/genética , Antibacterianos/metabolismo , Péptidos Catiónicos Antimicrobianos/genética , Bacterias/metabolismo , Señales de Clasificación de Proteína/genética , Piel/metabolismo , Proteínas Anfibias/metabolismo , Anfibios/metabolismo , Animales , Péptidos Catiónicos Antimicrobianos/metabolismo
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