Biology 1002B Lecture Notes - Lecture 19: Chlamydomonas, Phototaxis, Lysis
Document Summary
Grind up -eyespot, gather proteins from there. Study the protein to look at biological function. Use mutant (that could not respond to light) to see what codes for channelrhodopsin. Wants to study gene instead of protein. Much harder to go from protein sequence to gene sequence. More than one codon can code for the same amino acid. Dna equivalent to the mrna (codons need to make the functional protein) 2 genes are fused together, makes one protein (translated together) It becomes a chimeric protein due to attachment of eyfp. Not always the case, most of the time sticking another protein on interferes with the function of the original protein. Do this so you can track chr2. Use light to excite yfp (different wavelength from channelrhodopsin) Repository or molecular information (dna, proteins, genome) Lots of sequences available (easier and cheaper to sequence genome) The sequence is great, but we need the actual piece of dna.