The present invention is directed to the identification and use of ribonucleoside analogs to induce the mutation of an RNA virus, including BVDV, HIV and HCV, or a virus which otherwise replicates through an RNA intermediate. The increase in the mutation rate of the virus results in reduced viability of progeny generations of the virus, thereby inhibiting viral replication. In addition to these methods and related compositions, the invention provides methods and combinatorial chemistry libraries for screening ribonucleoside analogs for mutagenic potential.
Ancestral And Cot Viral Sequences, Proteins And Immunogenic Compositions
James I. Mullins - Seattle WA, US Allen G. Rodrigo - Auckland, NZ Gerald H. Learn - Kingston WA, US Fusheng Li - Seattle WA, US David C. Nickle - Seattle WA, US Mark A. Jensen - Snohomish WA, US
Assignee:
University of Washington - Seattle WA
International Classification:
C07H 21/02 C12N 15/00 C12N 1/20
US Classification:
536 231, 4353201, 4352523
Abstract:
The present invention is directed to ancestral and COT nucleic acid and amino acid sequences, methods for producing such sequences and uses thereof, including prophylactic and diagnostic uses.
The present invention is directed to ancestral HIV and FIV nucleic acid and amino acid sequences, methods for producing such sequences and uses thereof, including prophylactic and diagnostic uses.
Allen Rodrigo - , US Howard Ross - , US James Mullins - Seattle WA, US
International Classification:
C07H021/04 C12N007/00
US Classification:
536/023720, 435/235100
Abstract:
The present invention is directed to ancestral viral nucleic acid and amino acid sequences, methods for producing such sequences and uses thereof, including prophylactic and diagnostic uses.
Induction Of Viral Mutation By Incorporation Of Miscoding Ribonucleoside Analogs Into Viral Rna
Lawrence Loeb - Bellevue WA, US James Mullins - Seattle WA, US
Assignee:
University of Washington - Seattle WA
International Classification:
A61K048/00 C12N015/86 C12N007/00
US Classification:
514044000, 435235100, 435456000
Abstract:
The present invention is directed to the identification and use of ribonucleoside analogs to induce the mutation of an RNA virus, including BVDV, HIV and HCV, or a virus which otherwise replicates through an RNA intermediate. The increase in the mutation rate of the virus results in reduced viability of progeny generations of the virus, thereby inhibiting viral replication. In addition to these methods and related compositions, the invention provides methods and combinatorial chemistry libraries for screening ribonucleoside analogs for mutagenic potential.
The present invention is directed to ancestral HIV nucleic acid and amino acid sequences, methods for producing such sequences and uses thereof, including prophylactic and diagnostic uses.
Conserved-Element Vaccines And Methods For Designing Conserved-Element Vaccines
James Mullins - Seattle WA, US David Nickle - Seattle WA, US Morgane Rolland - Seattle MA, US
International Classification:
A61K 39/00 G06F 19/00
US Classification:
4241881, 702 20
Abstract:
Embodiments of the present invention include conserved-element vaccines and methods for designing and producing conserved-element vaccines. A conserved-element vaccine (“CEVac”) is a recombinant and/or synthetic vaccine that incorporates only highly conserved epitopes from an observed set of pathogen variants. The conserved epitopes are identified computationally by aligning biopolymer sequences, such as concatenated polypeptide sequences that together represent a pathogen proteome, corresponding to an observed set of pathogen variants, and computationally selecting conserved subsequences according to a number of subsequence-selection criteria. These subsequence-selection criteria may include a minimum conserved-subsequence length, a threshold frequency of occurrence of a particular monomer at each conserved, single-monomer position within a conserved subsequence, a threshold combined occurrence for a set of allowable variant monomers at a particular conserved, variable position within a conserved subsequence, and a maximum number of variable positions within a subsequence. A set of conserved subsequences identified according to the subsequence-selection criteria are then filtered to remove subsequences identical to, or too similar to, naturally-occurring host subsequences, and are then assembled into expression vectors for incorporation into microbial hosts for biosynthesis of a recombinant CEVac or assembled into one or more synthetic constructs for a synthetic CEVac.
Conserved-Element Vaccines And Methods For Designing Conserved-Element Vaccines
James Mullins - Seattle WA, US David Nickle - Seattle WA, US Morgane Rolland - Seattle WA, US
Assignee:
higher education - Seattle WA
International Classification:
C07K 7/08 C07K 7/06 G06N 5/00 C07H 21/04
US Classification:
530326, 530327, 536 2372, 530328, 706 46
Abstract:
Embodiments of the present invention include conserved-element vaccines and methods for designing and producing conserved-element vaccines. A conserved-element vaccine (“CEVac”) is a recombinant and/or synthetic vaccine that incorporates only highly conserved epitopes from an observed set of pathogen variants. The conserved epitopes are identified computationally by aligning biopolymer sequences, such as concatenated polypeptide sequences that together represent a pathogen proteome, corresponding to an observed set of pathogen variants, and computationally selecting conserved subsequences according to a number of subsequence-selection criteria. These subsequence-selection criteria may include a minimum conserved-subsequence length, a threshold frequency of occurrence of a particular monomer at each conserved, single-monomer position within a conserved subsequence, a threshold combined occurrence for a set of allowable variant monomers at a particular conserved, variable position within a conserved subsequence, and a maximum number of variable positions within a subsequence. A set of conserved subsequences identified according to the subsequence-selection criteria are then filtered to remove subsequences identical to, or too similar to, naturally-occurring host subsequences, and are then assembled into expression vectors for incorporation into microbial hosts for biosynthesis of a recombinant CEVac or assembled into one or more synthetic constructs for a synthetic CEVac.
Midland and Big Time AJ in Houston. We had a contingent from Central Texas and one from West Texas, two statewide candidates (Dan Branch and Harvey Hilderbran) and we had logic, food, music (with the wonderful talent of James Mullins), and political discussion! I think we will do it again.
Date: Jan 20, 2014
Category: U.S.
Source: Google
Researchers come a step closer to finding HIV vaccine
James Mullins, UW professor of microbiology, medicine and laboratory medicine, leads one of the two laboratories that did genetic analyses of the virus. He said the study proved that an HIV vaccine is within reach.
Date: Sep 15, 2012
Category: Health
Source: Google
Youtube
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Here's me beating the gong. A very tough, intimidating night,but manag...
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Because he lives James Mullins
Gospel music.
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James mullins
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Joy ( feat. Catherine Mullins)
Eddie James.
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The Law Offices Of James M. Mullins, Jr. PLLC...
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