User:Jrfisher: Difference between revisions

From OpenWetWare
Jump to navigationJump to search
 
(7 intermediate revisions by 2 users not shown)
Line 1: Line 1:
{{KeatingLabToolbar}}
{| width="100%"
| [[Image:Jfisher portrait small.jpg|frame|left|Jeremy]]
'''Jeremy Fisher'''


[[Image:Jfisher portrait small.jpg|frame|left|Jeremy]]
Technical Assistant<br>
 
77 Mass. Ave. Bldng 68-616D<br>
== Jeremy Fisher ==
 
Technical Assistant
 
Jeremy Fisher
 
77 Mass. Ave. Bldng 68-616D
Cambridge Mass. 02139
Cambridge Mass. 02139


 
email: jrfisher@mit.edu<br>
email: jrfisher@mit.edu
phone: 617 452 4101
phone: 617 452 4101
| {{KeatingLabToolbar}}
|}


 
== Bio ==
2002 B.S. Biochemistry, University of New Hampshire (UNH)
2002 B.S. Biochemistry, University of New Hampshire (UNH)


Line 26: Line 22:
"Isolation and Characterization of Leucine-Rich Repeat (LRR) Binding Peptides"
"Isolation and Characterization of Leucine-Rich Repeat (LRR) Binding Peptides"


<br><br><br><br><br>
<br><br>
 
==Intro==
==Intro==
Technical assistant and safety representative, for the Keating lab since summer of 2004. I mainly troubleshoot and optimize molecular biology, protein purification and protein binding experiments.
Technical assistant and safety representative, for the Keating lab since summer of 2004. I mainly troubleshoot and optimize molecular biology, protein purification and protein binding experiments.


== Research ==
== Research ==
'''I.) Explore High-Throughput techniques of protein purification'''
A vacuum manifold coupled with a series of 96 well filter plates is used to control the flow of dual affinity tagged proteins over corresponding affinity resins
Proteins are then transferred to a UV acceptable 96 well plate and lyophilized. This method permits the use of any buffer to re-suspend proteins and determine concentration
The 96 well of pure proteins can then be used to perform experiments to analyze protein-protein interactions 
PHOTO of APPARATUS
'''Millipore Multi-screen HTS vacuum manifold'''
'''II.) Bcl-2/BH3 Interaction Profiles and Specificity Determinants'''
Purify a panel of human and murine BH3-only peptides and mutants to test binding specificities against a subset of Bcl-2 family proteins. Identify amino acids important for various interactions.
'''III.) Identify and Characterize viral bZIP and human bZIP coiled coil interactions'''
Purify several human bZIP’s and viral bZIP’s coiled coil regions to experimentally determine and characterize homo and hetero-dimeric interactions. Generate a series of mutations and designed coiled coil peptides to identify key binding residues and the biochemical composition of interaction interfaces.


== Interests ==
== Interests ==

Latest revision as of 18:35, 22 November 2005

Jeremy

Jeremy Fisher

Technical Assistant
77 Mass. Ave. Bldng 68-616D
Cambridge Mass. 02139

email: jrfisher@mit.edu
phone: 617 452 4101

Information concerning the
Keating Lab
Research

Lab Members

Resources:
Publications
Experimental Protocols
Coder's Corner
Internal

Bio

2002 B.S. Biochemistry, University of New Hampshire (UNH)

"Two-Hybrid Analysis of LRR-Binding Peptides"


2004 M.S. Biochemistry and Molecular Biology, UNH,

"Isolation and Characterization of Leucine-Rich Repeat (LRR) Binding Peptides"



Intro

Technical assistant and safety representative, for the Keating lab since summer of 2004. I mainly troubleshoot and optimize molecular biology, protein purification and protein binding experiments.

Research

I.) Explore High-Throughput techniques of protein purification

A vacuum manifold coupled with a series of 96 well filter plates is used to control the flow of dual affinity tagged proteins over corresponding affinity resins

Proteins are then transferred to a UV acceptable 96 well plate and lyophilized. This method permits the use of any buffer to re-suspend proteins and determine concentration

The 96 well of pure proteins can then be used to perform experiments to analyze protein-protein interactions

PHOTO of APPARATUS







Millipore Multi-screen HTS vacuum manifold


II.) Bcl-2/BH3 Interaction Profiles and Specificity Determinants

Purify a panel of human and murine BH3-only peptides and mutants to test binding specificities against a subset of Bcl-2 family proteins. Identify amino acids important for various interactions.

III.) Identify and Characterize viral bZIP and human bZIP coiled coil interactions Purify several human bZIP’s and viral bZIP’s coiled coil regions to experimentally determine and characterize homo and hetero-dimeric interactions. Generate a series of mutations and designed coiled coil peptides to identify key binding residues and the biochemical composition of interaction interfaces.

Interests