Literature DB >> 28470596

N- and C-Terminal Truncations to Enhance Protein Solubility and Crystallization: Predicting Protein Domain Boundaries with Bioinformatics Tools.

Christopher D O Cooper1, Brian D Marsden2,3.   

Abstract

Soluble protein expression is a key requirement for biochemical and structural biology approaches to study biological systems in vitro. Production of sufficient quantities may not always be achievable if proteins are poorly soluble which is frequently determined by physico-chemical parameters such as intrinsic disorder. It is well known that discrete protein domains often have a greater likelihood of high-level soluble expression and crystallizability. Determination of such protein domain boundaries can be challenging for novel proteins. Here, we outline the application of bioinformatics tools to facilitate the prediction of potential protein domain boundaries, which can then be used in designing expression construct boundaries for parallelized screening in a range of heterologous expression systems.

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Keywords:  Alignment; BLAST; Bioinformatics; Domain; Hidden Markov Model (HMM); PSIPRED; Protein expression; Protein solubility; Protein structure; Secondary structure

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Year:  2017        PMID: 28470596     DOI: 10.1007/978-1-4939-6887-9_2

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  2 in total

1.  A tyrosinase, mTyr-CNK, that is functionally available as a monophenol monooxygenase.

Authors:  Hyunsu Do; Eungsu Kang; Byeongseon Yang; Hyung Joon Cha; Yoo Seong Choi
Journal:  Sci Rep       Date:  2017-12-08       Impact factor: 4.379

2.  Improved Plasmid-Based Inducible and Constitutive Gene Expression in Corynebacterium glutamicum.

Authors:  Nadja A Henke; Irene Krahn; Volker F Wendisch
Journal:  Microorganisms       Date:  2021-01-19
  2 in total

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