Core D provides technical expertise and state of the art molecular and cellular biology methodology for? cloning and expression of the proteins described in the program project. This centralized operation coordinates? all molecular biology work and ensures that all proteins are cloned and expressed in a uniform? fashion. This is particularly important since several investigators plan to analyze different aspects of some of? the same proteins. This uniformity greatly enhances accuracy of comparison between the proteins.? Core D designs and clones expression vectors encoding wild type or mutated proteins as requested by the? individual investigators. All wild type genes described in this program project are identified, sequenced and? assembled in cloning vectors. Thus, vectors expressing wild type or mutated proteins can be cloned from? cDNAs. Vectors expressing consensus sequence peptides will be constructed from synthetic? oligonucleotides. Depending on the requirement for the analysis of the protein (amount and/or modification of? protein), the expression vectors are designed for expression in prokaryotic or eukaryotic cell lines. Core D? also establishes cell lines expressing the proteins, determines conditions for optimum protein expression and? aids in the purification of the expressed protein.? Thus the service of Core D includes: a) advice toward an optimal expression system, b) design? methodologies to express desired proteins, c) confirm wild type DNA sequence by restriction and/or DNA? sequence analysis, d) design primers for DNA sequence analysis, e) design primers for PCR amplification of? wild type or mutant constructs, f) extract DNA, g) digest DNA with restriction enzymes, h) amplify DNA by? PCR, i) ligate DNA (fragments) in cloning and expression vectors, j) transform/transfect ligated DNA into cell? lines to express the proteins, k) select clones, I) amplify clones, m) isolate permanently transfected cell lines,? n) maintain transformed cell lines, o) establish optimum protein expression conditions, p) assist in protein? purification, q) maintain cell lines carrying wild type and expression vectors.? All personnel in Core D trains new users associated with the projects in molecular biology and cell culture? techniques and oversees proper use of cell culture facilities. This ensures safe maintenance of cell systems? and guarantees compliance with NIH guidelines.? Core D designs and clones expression vectors encoding proteins requested by the principal investigators of? the individual projects. They establish cell lines, determine optimum conditions for protein expression and aid? in the purification of the expressed protein.?

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
2P01HL026335-26
Application #
7140015
Study Section
Heart, Lung, and Blood Initial Review Group (HLBP)
Project Start
2006-01-01
Project End
2010-12-31
Budget Start
2006-01-01
Budget End
2007-01-31
Support Year
26
Fiscal Year
2006
Total Cost
$188,905
Indirect Cost
Name
Boston University
Department
Type
DUNS #
604483045
City
Boston
State
MA
Country
United States
Zip Code
02118
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Gursky, Olga (2013) Crystal structure of ?(185-243)ApoA-I suggests a mechanistic framework for the protein adaptation to the changing lipid load in good cholesterol: from flatland to sphereland via double belt, belt buckle, double hairpin and trefoil/tetrafoil. J Mol Biol 425:1-16
Khachfe, Hassan M; Atkinson, David (2013) Conformation and stability properties of B17: II. Analytical investigations using differential scanning calorimetry. Eur Biophys J 42:309-14
Meyers, Nathan L; Wang, Libo; Small, Donald M (2012) Apolipoprotein C-I binds more strongly to phospholipid/triolein/water than triolein/water interfaces: a possible model for inhibiting cholesterol ester transfer protein activity and triacylglycerol-rich lipoprotein uptake. Biochemistry 51:1238-48

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