ASU Regents' Professors Open Access Works

The membrane proximal region (MPR, residues 649–683) and transmembrane domain (TMD, residues 684–705) of the gp41 subunit of HIV-1’s envelope protein are highly conserved and are important in viral mucosal transmission, virus attachment and membrane fusion with target cells. Several structures of the trimeric membrane proximal external region (residues 662–683) of MPR have been reported at the atomic level; however, the atomic structure of the TMD still remains unknown. To elucidate the structure of both MPR and TMD, we expressed the region spanning both domains, MPR-TM (residues 649–705), in Escherichia coli as a fusion protein with maltose binding protein (MBP). MPR-TM was initially fused to the C-terminus of MBP via a 42 aa-long linker containing a TEV protease recognition site (MBP-linker-MPR-TM).

Biophysical characterization indicated that the purified MBP-linker-MPR-TM protein was a monodisperse and stable candidate for crystallization. However, crystals of the MBP-linker-MPR-TM protein could not be obtained in extensive crystallization screens. It is possible that the 42 residue-long linker between MBP and MPR-TM was interfering with crystal formation. To test this hypothesis, the 42 residue-long linker was replaced with three alanine residues. The fusion protein, MBP-AAA-MPR-TM, was similarly purified and characterized. Significantly, both the MBP-linker-MPR-TM and MBP-AAA-MPR-TM proteins strongly interacted with broadly neutralizing monoclonal antibodies 2F5 and 4E10. With epitopes accessible to the broadly neutralizing antibodies, these MBP/MPR-TM recombinant proteins may be in immunologically relevant conformations that mimic a pre-hairpin intermediate of gp41.

Aim
To establish a chronology for late Quaternary avian extinction, extirpation and persistence in the Bahamas, thereby testing the relative roles of climate change and human impact as causes of extinction.
Location
Great Abaco Island (Abaco), Bahamas, West Indies.
Methods
We analysed the resident bird community as sampled by Pleistocene (> 11.7 ka) and Holocene (< 11.7 ka) fossils. Each species was classified as extinct (lost globally), extirpated (gone from Abaco but persists elsewhere), or extant (still resident on Abaco). We compared patterns of extinction, extirpation and persistence to independent estimates of climate and sea level for glacial (late Pleistocene) and interglacial (Holocene) times.
Results
Of 45 bird species identified in Pleistocene fossils, 25 (56%) no longer occur on Abaco (21 extirpated, 4 extinct). Of 37 species recorded in Holocene deposits, 15 (14 extirpated, 1 extinct; total 41%) no longer exist on Abaco. Of the 30 extant species, 12 were recovered as both Pleistocene and Holocene fossils, as were 9 of the 30 extirpated or extinct species. Most of the extinct or extirpated species that were only recorded from Pleistocene contexts are characteristic of open habitats (pine woodlands or grasslands); several of the extirpated species are currently found only where winters are cooler than in the modern or Pleistocene Bahamas. In contrast, most of the extinct or extirpated species recorded from Holocene contexts are habitat generalists.
Main conclusions
The fossil evidence suggests two main times of late Quaternary avian extirpation and extinction in the Bahamas. The first was during the Pleistocene–Holocene transition (PHT; 15–9 ka) and was fuelled by climate change and associated changes in sea level and island area. The second took place during the late Holocene (< 4 ka, perhaps primarily < 1 ka) and can be attributed to human impact. Although some species lost during the PHT are currently found where climates are cooler and drier than in the Bahamas today, a taxonomically and ecologically diverse set of species persisted through that major climate change but did not survive the past millennium of human presence.

Viral protein U (Vpu) is a type-III integral membrane protein encoded by Human Immunodeficiency Virus-1 (HIV- 1). It is expressed in infected host cells and plays several roles in viral progeny escape from infected cells, including down-regulation of CD4 receptors. But key structure/function questions remain regarding the mechanisms by which the Vpu protein contributes to HIV-1 pathogenesis. Here we describe expression of Vpu in bacteria, its purification and characterization. We report the successful expression of PelB-Vpu in Escherichia coli using the leader peptide pectate lyase B (PelB) from Erwinia carotovora. The protein was detergent extractable and could be isolated in a very pure form. We demonstrate that the PelB signal peptide successfully targets Vpu to the cell membranes and inserts it as a type I membrane protein. PelB-Vpu was biophysically characterized by circular dichroism and dynamic light scattering experiments and was shown to be an excellent candidate for elucidating structural models.