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HIV Attachment and Entry: Pursuing a Challenging Target

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Presentation on theme: "HIV Attachment and Entry: Pursuing a Challenging Target"— Presentation transcript:

1 HIV Attachment and Entry: Pursuing a Challenging Target

2 Introduction

3 This program will include a discussion of data that were presented in abstract form. These data should be considered preliminary until published in a peer-reviewed journal.

4 HIV-1 Entry: The First Step in the HIV-1 Life Cycle

5 Key Viral Protein for HIV Entry

6 HIV-1 Immune Pressure and Evasion

7 Overall Outline of Type 1 Fusion Mechanism of HIV-1 Entry Resolved 20 Years Ago

8 HIV-1 Env Entry Pathway Contains Additional Prefusion States

9 Understand Entry and Immune Evasion With Atomic-Level Insights

10 Understand Entry and Immune Evasion with Atomic-Level Insights (cont)

11 Outline

12 Link Ligand-Induced States to smFRET Measurements

13 smFRET Tags in V1-V4 Sample Conformational Flexibility of HIV-1 Env Trimer on Infectious Virus

14 Functional Env Trimer Transitions Between 3 Prefusion Conformation States

15 State 1 Was Preferentially Recognized by Most Broadly Neutralizing Antibodies

16 Determination of Env Trimer Structure Used 2 Antibodies for Crystallization

17 Initial Interaction of CD4 With the HIV-1 Env Trimer

18 Measurement of smFRET Directly on Soluble Env Trimers

19 Insights on Structure of Env Trimers

20 Structural Transformation: State 2 to State 3

21 Summary: HIV-1 Env Structure

22 Outline

23 Inhibitors That Bind to States 1 and 2 Neutralize Primary Isolates; Those That Only Bind State 3 Often Do Not

24 Entry Inhibitors and Targets

25 Fostemsavir (BMS )

26 Fostemsavir: BRIGHTE Phase 3 Study

27 Crystal Structures of HIV-1-Env Trimer With BMS-378806 and Its Derivative, Temsavir

28 Lattice-Chaperone Strategy: Mutations for Improvement

29 Summary: Chaperone Mutations for Improvement

30 New Lattice Appears to Be Improved

31 New Crystal Allows for the Determination of Structures With Trimers From Diverse HIV-1 Strains

32 Co-Crystal Structures Show Potential Additional Functional Group

33 Structural "Freezing" by Temsavir Binding

34 Summary: Small Molecule Entry Inhibitors

35 Concluding Remarks

36 Abbreviations


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