RU2015119440A - Стабильные и растворимые антитела - Google Patents

Стабильные и растворимые антитела Download PDF

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RU2015119440A
RU2015119440A RU2015119440/10A RU2015119440A RU2015119440A RU 2015119440 A RU2015119440 A RU 2015119440A RU 2015119440/10 A RU2015119440/10 A RU 2015119440/10A RU 2015119440 A RU2015119440 A RU 2015119440A RU 2015119440 A RU2015119440 A RU 2015119440A
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Леонардо БОРРАС
Дэвид УРЕХ
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ИЭсБиЭйТЕК - Э НОВАРТИС КОМПАНИ ЭлЭлСи
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/395Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P27/00Drugs for disorders of the senses
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    • A61P27/04Artificial tears; Irrigation solutions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • A61P27/06Antiglaucoma agents or miotics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • A61P27/14Decongestants or antiallergics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/24Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against cytokines, lymphokines or interferons
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/24Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against cytokines, lymphokines or interferons
    • C07K16/241Tumor Necrosis Factors
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/20Immunoglobulins specific features characterized by taxonomic origin
    • C07K2317/24Immunoglobulins specific features characterized by taxonomic origin containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/30Immunoglobulins specific features characterized by aspects of specificity or valency
    • C07K2317/31Immunoglobulins specific features characterized by aspects of specificity or valency multispecific
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/50Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/56Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/60Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments
    • C07K2317/62Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments comprising only variable region components
    • C07K2317/622Single chain antibody (scFv)
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/70Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/76Antagonist effect on antigen, e.g. neutralization or inhibition of binding
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/90Immunoglobulins specific features characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin
    • C07K2317/94Stability, e.g. half-life, pH, temperature or enzyme-resistance

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  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
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  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
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Abstract

1. Способ уменьшения способности агрегации антитела, которое представляет собой гетеродимерный комплекс, включающий вариабельный домен легкой цепи и вариабельный домен тяжелой цепи, где способ включает стадии:(а) обеспечения полного атомно-молекулярного представления антитела;(b) определения свободной энергии взаимодействия двух доменов;(c) выбора одного или более аминокислотных остатков, участвующих во взаимодействии, для замены посредством предоставления молекулярной модели антитела, содержащего одну или более замен в выбранных положениях, и определения свободной энергии взаимодействия в представлении молекулы с заменой(ами);(d) выбора аминокислотного остатка для замены, если свободная энергия взаимодействия в модели молекулы с заменой(ами) меньше свободной энергии взаимодействия в исходной молекулярной модели.2. Способ по п. 1, в котором свободную энергию взаимодействия определяют с помощью расчета разницы между энергией комплекса и суммой энергий отдельных доменов в рамках способа с использованием неявно заданного растворителя.3. Способ по п. 2, в котором растворителем является GBMV или PBSA.4. Способ по п. 1, дополнительно включающий стадию(i) моделирования распределения зарядов в белке, причем эту стадию выполняют в рамках стадии a и b.5. Способ по п. 4, в котором моделирование распределения зарядов осуществляют на основе электростатических сил или сил Ван-дер-Ваальса.6. Способ по п. 1, в котором стадия (c) включает дополнительную стадию минимизации энергии в области вокруг мутации.7. Способ по п. 1, в котором антителом является одноцепочечный Fv-фрагмент (scFv).

Claims (7)

1. Способ уменьшения способности агрегации антитела, которое представляет собой гетеродимерный комплекс, включающий вариабельный домен легкой цепи и вариабельный домен тяжелой цепи, где способ включает стадии:
(а) обеспечения полного атомно-молекулярного представления антитела;
(b) определения свободной энергии взаимодействия двух доменов;
(c) выбора одного или более аминокислотных остатков, участвующих во взаимодействии, для замены посредством предоставления молекулярной модели антитела, содержащего одну или более замен в выбранных положениях, и определения свободной энергии взаимодействия в представлении молекулы с заменой(ами);
(d) выбора аминокислотного остатка для замены, если свободная энергия взаимодействия в модели молекулы с заменой(ами) меньше свободной энергии взаимодействия в исходной молекулярной модели.
2. Способ по п. 1, в котором свободную энергию взаимодействия определяют с помощью расчета разницы между энергией комплекса и суммой энергий отдельных доменов в рамках способа с использованием неявно заданного растворителя.
3. Способ по п. 2, в котором растворителем является GBMV или PBSA.
4. Способ по п. 1, дополнительно включающий стадию
(i) моделирования распределения зарядов в белке, причем эту стадию выполняют в рамках стадии a и b.
5. Способ по п. 4, в котором моделирование распределения зарядов осуществляют на основе электростатических сил или сил Ван-дер-Ваальса.
6. Способ по п. 1, в котором стадия (c) включает дополнительную стадию минимизации энергии в области вокруг мутации.
7. Способ по п. 1, в котором антителом является одноцепочечный Fv-фрагмент (scFv).
RU2015119440/10A 2010-10-22 2011-10-24 Стабильные и растворимые антитела RU2015119440A (ru)

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US40579810P 2010-10-22 2010-10-22
US61/405,798 2010-10-22
US201161484749P 2011-05-11 2011-05-11
US61/484,749 2011-05-11

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