. If we increase the concentration of NaCl how will change the binding of our transcription factor to the DNA? How will change the melting point of DNA? Of course, explain.
1. With increasing salt concentration, ions concentration inctreases. With increasing ion concentration, the ions can actually intercat with the receptor in a way that competes with the ligands. Also, the ions in the salty solution assemble in a screeing cloud around the macromolecule that have the potential to bind. When this binding reaction occurs, tehre is relese of ions in the screening cloud, whihc results in an entropy increase. Moreover, thermodynamic data suggests that the protein-DNA interaction at high salt concentration is accompanied by the removal of large numbers of water molecules from the buried hydrophobic surface area. In addition, the involvement of ions appears to influence the binding which can be explained by binding of cations in the interface between the electrostatically negative lateral lobes on the protein and the negatively charged DNA.
. If we increase the concentration of NaCl how will change the binding of our transcription...
Certain laboratories often need to prepare DNA duplexes for transcription factor binding assays. The DNA is purchased as single-stranded polynucleotides and hybridize them to form our duplexes, but this almost always leaves behind some un-renatured, single-stranded DNA, in the solution. How would you go about removing the single-stranded DNA fromour duplexes?
The hunchback gene has an enhancer containing 3 binding sites for the transcription factor Bicoid. How could the loss of a single DNA binding site -leaving the 2 others intact- act to reduce gene expression of hunchback by more than 1/3 ? A. Bound Bicoid transcription factor molecules interact antagonistically to cause maximal gene expression B. Bound Bicoid transcription factor molecules interact additively to cause maximal gene expression C. Bicoid does not bind to the hunchback enhancer D. Bound Bicoid...
How will you determine the transcription factor binding sites in the whole genome? Give at least one example from literature.
How does the Trp repressor prevents RNA polymerase from initiating transcription? by blocking the ribosome binding site by forming a loop in the operator that restricts the passage of the polymerase by binding to the polymerase to inhibit its catalytic activity by physically blocking the DNA binding site of RNA polymerase
Looking at the diagram of transcription in eukaryotes and using the information provided, how could the expression of lactase RNA be turned on and off by transcription factors, activators and repressors? Styles Font Paragraph Activators bind to genes at Rapressors bind to genes seauences and at shaoser sequences and The expression of RNA in eukaryotes is initiated by the binding of basal transcription factors to the promoter sequence of a gene. This leads to the recruitment of RNA polymerase to...
How does ribosome binding affect the final level of protein produced from a DNA sequence? Only one question at a time; only one chance to answer. Question 1 0.5 pts How does ribosome binding affect the final level of protein produced from a DNA sequence? determines the efficiency of transcription factor bindings determines how many proteins can be made from each mRNA determines mRNA stabiity determines teh rate of nuclear transport of mRNAS
How does the change in pH from 7.2 to 8.2 affect the binding of BPG to the central cavity of Hemoglobin's T state? Is it no effect, increase or decrease binding? Explain why.
BIOCHEMISTRY HELP ASAP PLEASE!!! Question 7 3 pts The transcription and production of a protein called interferon-beta (FNB) is regulated VF-Blevel by a transcription factor called IRF3 which binds to DNA as a dimer of two 30KD Mutation monomeric proteins. The DNA-binding site of RF3 contains the following amino acids. Nere Arg - Lys - lle - Thr. I create four mutants of IRF3 by changing one of the amino acids of AD the DNA-binding site to serine, and then...
How quality and safety affect our patients. How we can change that
Recrystallization of Acetanilide was conducted using water as our solvent. First we had to choose a solvent based (water was chosen as our solvent due to it not dissolving acetanilide at room temp but dissolved it when heated) Then we performed recrystallizaation, vacuum filtration and then melting point measurements. For the post lab discussion for recrystallization of acetanilide report we have to address several different arguments. The ones below I'm not sure what to focus on to completely defend what...