The Molecular Biology Core has been in operation for the past twelve years and has provided state-ofthe-art methodologies for numerous molecular biological techniques and recombinant protein expression andpurification. The major goals of the Molecular Biology Core remain:1. To collect and maintain suitable plasmid vectors and host for expression of HIV/SIV and relatedrecombinant proteins2. To provide a service for construction of recombinant plasmids and high level expression of HIV/SIVand related proteins, including HLA tetramers for immunological analysis.3. To provide a service for purification of HIV/SIV and related proteins.4. To establish an onsite repository for plasmids with HIV/SIV genes as well as recombinant HIV/SIVproteins.5. To provide a service for construction of infectious HIVISIV proviral clones containing definedmutations in genes of interest.6. To train personnel to assist in the various phases of plasmid construction and expression/purificationof recombinant proteins for the purpose of facilitating technology transfer.The Molecular Biology Core has assisted, on average, over 25 CFAR members per year during the lastfunding period. The Core has averaged over $40,000 per year in chargebacks over the last funding period($180,000 total). The Molecular Biology Core has provided critical reagents and expertise to UAB CFARmembers that have funded individual R01 grants, UAB's National Corporative Vaccine Development Groupand a multi-investigator funded program project to elucidate features of the HIV-1 reverse transcription. Inthe next funding period, the Core will expand its efforts to provide critical reagents for the international CFARtransmission and vaccine initiatives. Support of this facility is thus instrumental for the continued success ofnumerous investigators working in different areas of HIV pathogenesis, vaccine and therapeuticdevelopment currently conducted at UAB.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Center Core Grants (P30)
Project #
3P30AI027767-20S1
Application #
7697009
Study Section
Special Emphasis Panel (ZAI1-EC-A (J1))
Project Start
2008-09-16
Project End
2009-02-28
Budget Start
2008-09-16
Budget End
2009-02-28
Support Year
20
Fiscal Year
2008
Total Cost
$102,031
Indirect Cost
Name
University of Alabama Birmingham
Department
Type
DUNS #
063690705
City
Birmingham
State
AL
Country
United States
Zip Code
35294
Adeli, Ehsan; Kwon, Dongjin; Zhao, Qingyu et al. (2018) Chained regularization for identifying brain patterns specific to HIV infection. Neuroimage 183:425-437
Verma, Richa; Sahu, Rajnish; Dixit, Saurabh et al. (2018) The Chlamydia M278 Major Outer Membrane Peptide Encapsulated in the Poly(lactic acid)-Poly(ethylene glycol) Nanoparticulate Self-Adjuvanting Delivery System Protects Mice Against a Chlamydia muridarum Genital Tract Challenge by Stimulating Robust Systemic Front Immunol 9:2369
Grover, Surbhi; Desir, Fidel; Jing, Yuezhou et al. (2018) Reduced Cancer Survival Among Adults With HIV and AIDS-Defining Illnesses Despite No Difference in Cancer Stage at Diagnosis. J Acquir Immune Defic Syndr 79:421-429
Crockett, Kaylee B; Turan, Bulent (2018) Moment-to-moment changes in perceived social support and pain for men living with HIV: an experience sampling study. Pain 159:2503-2511
Carson, Tiffany L; Wang, Fuchenchu; Cui, Xiangqin et al. (2018) Associations Between Race, Perceived Psychological Stress, and the Gut Microbiota in a Sample of Generally Healthy Black and White Women: A Pilot Study on the Role of Race and Perceived Psychological Stress. Psychosom Med 80:640-648
Salantes, D Brenda; Zheng, Yu; Mampe, Felicity et al. (2018) HIV-1 latent reservoir size and diversity are stable following brief treatment interruption. J Clin Invest 128:3102-3115
Goodin, Burel R; Owens, Michael A; White, Dyan M et al. (2018) Intersectional health-related stigma in persons living with HIV and chronic pain: implications for depressive symptoms. AIDS Care 30:66-73
Jiang, Wei; Luo, Zhenwu; Martin, Lisa et al. (2018) Drug Use is Associated with Anti-CD4 IgG-mediated CD4+ T Cell Death and Poor CD4+ T Cell Recovery in Viral-suppressive HIV-infected Individuals Under Antiretroviral Therapy. Curr HIV Res 16:143-150
Bilal, Usama; McCaul, Mary E; Crane, Heidi M et al. (2018) Predictors of Longitudinal Trajectories of Alcohol Consumption in People with HIV. Alcohol Clin Exp Res 42:561-570
Bekhbat, Mandakh; Mehta, C Christina; Kelly, Sean D et al. (2018) HIV and symptoms of depression are independently associated with impaired glucocorticoid signaling. Psychoneuroendocrinology 96:118-125

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