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Related Concept Videos

Genome Annotation and Assembly03:36

Genome Annotation and Assembly

The genome refers to all of the genetic material in an organism. It can range from a few million base pairs in microbial cells to several billion base pairs in many eukaryotic organisms. Genome assembly refers to the process of taking the DNA sequencing data and putting it all back together in a correct order to create a close representation of the original genome. This is followed by the identification of functional elements on the newly assembled genome, a process called genome annotation.
Protein Complexes with Interchangeable Parts01:57

Protein Complexes with Interchangeable Parts

Groups of proteins may form a complex where each protein in this complex has a different role in the overall execution of the complex’s function. Often some of the proteins in the complex can be replaced by a closely related variant to give a complex that contains many of the same components yet is functionally distinct.
The SCF ubiquitin ligase is a protein complex of five individual proteins. This complex attaches ubiquitin to other target proteins to mark them for degradation. In order to...
Assembly of Cytoskeletal Filaments01:18

Assembly of Cytoskeletal Filaments

Cytoskeletal filaments are polymeric forms of smaller protein subunits. However, individual cytoskeletal filaments may easily disassemble or associate with other similar filaments to form rigid structures. Microfilaments, made of actin monomers, rely on actin-binding proteins to form bundles and create networks of individual actin filaments. Microtubules rely on microtubule-associated proteins (MAPs) to form sturdy cylindrical structures. However, the proteins involved in forming complex...
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Assembly of Signaling Complexes

Multiprotein signaling complexes are formed in a dynamic process involving protein-protein interactions at the cytoplasmic domain of transmembrane receptors or enzymatic and non-enzymatic proteins associated with the receptor. These complexes ensure the activation and propagation of intracellular signals that regulate cell functions.
Interaction domains in cell signaling
Interaction domains recognize exposed features of their binding partners containing post-translationally modified sequences,...
Ligand Binding and Linkage00:49

Ligand Binding and Linkage

Allosteric proteins have more than one ligand binding site; the binding of a ligand to any of these sites influences the binding of ligands to the other sites. When a protein is allosteric, its binding sites are called coupled or linked.  In the case of enzymes, the site that binds to the substrate is known as the active site and the other site is known as the regulatory site. When a ligand binds to the regulatory site, this leads to conformational changes in the protein that can influence the...
Ligand Binding and Linkage00:49

Ligand Binding and Linkage

Allosteric proteins have more than one ligand binding site; the binding of a ligand to any of these sites influences the binding of ligands to the other sites. When a protein is allosteric, its binding sites are called coupled or linked.  In the case of enzymes, the site that binds to the substrate is known as the active site and the other site is known as the regulatory site. When a ligand binds to the regulatory site, this leads to conformational changes in the protein that can influence the...

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Related Experiment Video

Updated: Jun 15, 2026

Protocols for C-Brick DNA Standard Assembly Using Cpf1
12:03

Protocols for C-Brick DNA Standard Assembly Using Cpf1

Published on: June 15, 2017

BglBricks: A flexible standard for biological part assembly.

J Christopher Anderson1, John E Dueber, Mariana Leguia

  • 1Department of Bioengineering, University of California, Berkeley, CA 94720, USA. jcanderson@berkeley.edu

Journal of Biological Engineering
|March 9, 2010
PubMed
Summary

A new DNA assembly standard, BglBricks, overcomes limitations of older methods like BioBricks. This advance enables seamless construction of protein fusions and other synthetic biology applications.

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Area of Science:

  • Synthetic Biology
  • Molecular Biology
  • Bioengineering

Background:

  • Standard biological parts are foundational for synthetic biology, enabling applications in bioenergy, therapeutics, and environmental remediation.
  • The original BioBricks assembly standard has limitations, particularly its unsuitability for protein fusions due to an unfavorable scar sequence encoding a stop codon.

Purpose of the Study:

  • To introduce BglBricks, a novel DNA composition standard designed to address the scar translation issue in protein fusion construction.
  • To provide a more flexible and robust platform for generating standard biological parts and automating DNA assembly.

Main Methods:

  • Development of the BglBricks standard utilizing BglII and BamHI restriction enzymes.
  • Demonstration of the BglBricks system's utility in constructing gene expression devices, protein fusions, and targeted DNA integrations.

Main Results:

  • The BglBricks system creates a 6-nucleotide scar sequence encoding glycine-serine, a suitable peptide linker for protein fusions.
  • Successful construction of constitutively active gene expression devices with diverse expression profiles.
  • Demonstrated ability to create chimeric, multi-domain protein fusions and integrate DNA sequences into specific genomic loci.

Conclusions:

  • The BglBricks standard offers a more flexible platform for biological part generation and DNA assembly automation.
  • Ongoing development of BglBrick assembly reactions and associated automation/bioinformatics tools aims to streamline genetic engineering.
  • This advancement facilitates the transformation of genetic engineering into a design-based discipline.