20.109:Module 4: Difference between revisions

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==Module 4==
==Module 4==


'''Instructors:''' Angela Belcher and [[Natalie Kuldell]]
'''Instructors:''' [[Angela Belcher]] and [[Natalie Kuldell]]


'''TA:''' [[Chandni Valiathan]]
'''TA:''' [[Chandni Valiathan]]
In this experimental module we will study an unusual protein, one that allows yeast to bind a metal, gold. Over the next few weeks we will purify yeast based on this binding property, and then we’ll vary some experimental condition to improve the yeast/gold interaction. Using your optimized conditions, we will screen a library of yeast to isolate a new gold-binding strain. The DNA encoding the new gold-binding protein will be sequenced and, with any luck, we’ll elucidate some amino acid requirements for the yeast/metal interaction.
[[Image:Macintosh HD-Users-nkuldell-Desktop-yeastbuddingandbound.png|center|400px|'''S. cerevisiae shown budding (top) and bound to CdS (bottom)''']]
[[20.109(S07):Bio-material engineering/Screening library | Module 4 Day 1: Screening library]]<br>
[[20.109(S07): Bio-material engineering/Optimizing panning | Module 4 Day 2: Optimizing panning]]<br>
[[20.109(S07): Bio-material engineering/Rescreening gold binders | Module 4 Day 3: Rescreening gold binders]]<br>
[[20.109(S07): Bio-material engineering/PCR of gold binding candidates | Module 4 Day 4: PCR of gold binding candidates]]<br>
[[20.109 (S07): Research proposal, module 4| Module 4 Day 5: Student presentations]]<br>
[[20.109(S07): Bio-material engineering/Sequence analysis | Module 4 Day 6: Sequence analysis]]<br>
[[20.109(S07): Biomaterial engineering, TA notes| TA notes Module 4]]

Latest revision as of 03:30, 17 April 2007


20.109: Laboratory Fundamentals of Biological Engineering

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Module 4

Instructors: Angela Belcher and Natalie Kuldell

TA: Chandni Valiathan

In this experimental module we will study an unusual protein, one that allows yeast to bind a metal, gold. Over the next few weeks we will purify yeast based on this binding property, and then we’ll vary some experimental condition to improve the yeast/gold interaction. Using your optimized conditions, we will screen a library of yeast to isolate a new gold-binding strain. The DNA encoding the new gold-binding protein will be sequenced and, with any luck, we’ll elucidate some amino acid requirements for the yeast/metal interaction.

S. cerevisiae shown budding (top) and bound to CdS (bottom)
S. cerevisiae shown budding (top) and bound to CdS (bottom)


Module 4 Day 1: Screening library
Module 4 Day 2: Optimizing panning
Module 4 Day 3: Rescreening gold binders
Module 4 Day 4: PCR of gold binding candidates
Module 4 Day 5: Student presentations
Module 4 Day 6: Sequence analysis
TA notes Module 4