Evidence map›Paper›PMID 42277315›Full record

ReviewNature reviews. Microbiology2026

Mechanisms of HIV-1 assembly, release and maturation.

Alex B Kleinpeter, Eric O Freed

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Alex B KleinpeterDepartment of Microbiology and Immunology, University of Iowa, Iowa City, IA, USA. alex-kleinpeter@uiowa.edu.ORCID http://orcid.org/0000-0001-5630-1345
Eric O FreedVirus-Cell Interaction Section, HIV Dynamics and Replication Program, Center for Cancer Research, National Cancer Institute, Frederick, MD, USA. efreed@mail.nih.gov.ORCID http://orcid.org/0000-0003-3345-022X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Over the past decade, major advances in structural biology and in vitro and cell-based technologies have enhanced our understanding of HIV-1 assembly, release and maturation. The cryo-electron microscopy revolution, alongside developments in single-molecule approaches and live-cell imaging techniques, have enabled researchers to visualize biological complexes at remarkably high resolution, reconstitute biochemical processes under physiologically relevant conditions and directly observe these processes in cells and virions. Effective integration of these methods with both classical and novel molecular virology approaches has yielded a wealth of basic knowledge that has driven the development of potent inhibitors targeting virus maturation and highlighted mechanisms by which events that take place late in the virus replication cycle prime newly formed virus particles for infection of a new host cell. This Review outlines the recent progress in elucidating the molecular underpinnings of the late stages of the HIV-1 replication cycle and highlights the interplay between virology, host cell biology and the development of antiretroviral compounds with therapeutic potential.

Indexed as

HIV-1HIV InfectionsVirus AssemblyVirus ReleaseCryoelectron MicroscopyHumansVirionVirus Replication

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.